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[CANCER RESEARCH 64, 1924 –1931, March 15, 2004] Advances in Brief Pol Is a Candidate for the Mouse Pulmonary Adenoma Resistance 2 Locus, a Major Modifier of Chemically Induced Lung Neoplasia Min Wang,1 Theodora R. Devereux,2 Haris G. Vikis,4 Scott D. McCulloch,3 Wanda Holliday,2 Colleen Anna,2 Yian Wang,1 Katarzyna Bebenek,3 Thomas A. Kunkel,3 Kunliang Guan,4 and Ming You1 1 Department of Surgery and The Alvin J. Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri; 2Laboratory of Molecular Carcinogenesis and Laboratory of Molecular Genetics and Laboratory of Structural Biology, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, North Carolina; and 4 Department of Biological Chemistry, University of Michigan, Ann Arbor, Michigan 3 Abstract In this study, we performed systematic candidate gene analyses of the Pulmonary adenoma resistance 2 locus. Differential gene expression in lung tissues and nucleotide polymorphisms in coding regions between A/J and BALB/cJ mice were examined using reverse transcription-PCR and direct sequencing. Although not all genes in the interval were analyzed at this moment due to the recent database updating, we have found that the Pol gene, encoding the DNA polymerase , contains 25 nucleotide polymorphisms in its coding region between A/J and BALB/cJ mice, resulting in a total of ten amino acid changes. Primer extension assays with purified BALB/cJ and A/J proteins in vitro demonstrate that both forms of Pol are active but that they may differ in substrate discrimination, which may affect the formation of Kras2 mutations in mouse lung tumors. Altered expression of POL protein and an amino acid-changing nucleotide polymorphism were observed in human lung cancer cells, suggesting a possible role in the development of lung cancer. Thus, our data support the Pol gene as a modifier of lung tumorigenesis by altering DNA polymerase activity. Introduction Lung cancer is the leading cause of cancer-related death in the United States (1). Although cigarette smoke is implicated in ⬃90% of male and 75– 80% of female lung cancer deaths, only ⬃15% of heavy smokers will ultimately develop lung cancer, which suggests that there is variation in individual susceptibility to lung cancer (2, 3). Inbred strains of mice vary markedly in their susceptibility to spontaneous and chemically induced lung tumorigenesis, thus representing a valuable model to study genetic susceptibility to lung cancer. On the basis of their mean tumor multiplicities induced by a lung carcinogen, the inbred mouse strains can be categorized into sensitive, intermediate, and resistant groups (4). The A strain is the most susceptible strain, whereas the C57BL/6J strain is the most resistant. Other strains such as the BALB/cJ strain belong to the intermediate group and are less susceptible to lung tumorigenesis than the A strain. Experimental crosses of inbred mouse strains have revealed Pulmonary adenoma susceptibility (Pas) loci, Pulmonary adenoma resistance (Par) loci, and Susceptibility to lung cancer (Slucs) loci (5). A/J and BALB/cJ inbred strains of mice carry the same Pas1 allele but show different susceptibility to urethane-induction of lung tumors. In (A/J ⫻ BALB/c) F1 mice, the relatively resistant BALB/cJ phe- notype was dominant over the high susceptibility of A/J mice (6). Additional analysis on F2 hybrids and backcross mice supported the hypothesis that a major locus named Par2 accounts for the difference in adenoma susceptibility between A/J mice and BALB/cJ mice (7). Par2 is mapped to the mouse chromosome 18 and accounts for 60% phenotype variance (7–9). The resistance of BALB/cJ mice appears due to the interaction between the Pas1 QTL and Par2 QTL in the BALB/cJ mouse genome (10). We previously used (A/J ⫻ BALB/ cJ) ⫻ BALB/cJ congenic mice to successfully fine map the Par2 locus into a candidate region encompassed by the D18Mit103 and D18Mit162 markers (11). In a recent study, this region has been additionally narrowed down to a region encompassed by the marker D18Mit103 and D18Mit188 (12), which has resulted in a ⬃2.4-Mb candidate region based on the Celera and public mouse genome databases. Four known genes are located in this region, i.e., StarD6, Pol , Mbd2, and Dcc. Preliminary analysis of the polymorphisms in the Dcc and Pol genes were reported recently (11, 13). Pol represents an interesting candidate for the Par2 locus. It is the most error-prone DNA polymerase and preferentially incorporates G rather than A across from template T (14 –16). Human POL has at least two distinct catalytic activities including translesion DNA synthesis and 5⬘-deoxyribose phosphate lyase activity (17–19). Its 5⬘-deoxyribose phosphate lyase activity and capability for filling short gaps implicate that this polymerase may play a role in certain base excision repair (BER) reactions (19). It may also play a role in lung tumorigenesis by affecting DNA adduct repair and thus Kras2 mutations that are found in a high proportion of mouse and human lung tumors (13, 20). In the present study, we identified multiple nucleotide polymorphisms and alternatively spliced transcript isoforms in the Pol gene between A/J and BALB/cJ mice. We provide initial biochemical support for the hypothesis that the amino acid differences between the two mouse isoforms may affect their substrate discrimination properties. An amino acid-changing nucleotide polymorphism and altered expression of POL protein in human lung cancer cell lines was observed. These data support the Pol gene as a modifier of lung tumorigenesis by altering DNA polymerase and, possibly, repair activity. Materials and Methods Expression and Nucleotide Polymorphism Analyses of Genes in the Par2 Region. Inbred mouse strains were purchased from The Jackson Laboratory (Bar Harbor, ME). DNA was isolated from tail snips. For RNA isolaReceived 9/30/03; revised 1/6/04; accepted 1/12/04. tion, 100 mg of lung tissue were pulverized and total RNA extracted using Grant support: NIH Grants R01CA099147 and R01CA58554. The costs of publication of this article were defrayed in part by the payment of page TRIzol reagent according to the manufacturer’s protocol (Life Technologies, charges. This article must therefore be hereby marked advertisement in accordance with Inc., Gaithersburg, MD). The quality of the isolated RNA was assessed by 18 U.S.C. Section 1734 solely to indicate this fact. absorbance at 260 nm, the A260/A280 ratio (1.7–1.9), and electrophoresis on Note: M. Wang, T. Devereux, and H. Vikis and their laboratories contributed equally 1% agarose/formaldehyde gels that indicated the intensity and integrity of the to this article. Data deposition: The Pol A/J and BALB/c coding sequences reported in this article have been deposited in the GenBank database (accession nos. AY515316 and 28S and 18S bands. Two g of total RNA were used in a reverse transcription AY515317). reaction to synthesize the first-strand cDNA using oligo-dT primer. Primers Requests for reprints: Ming You, Department of Surgery, The Washington Univerwere designed for each gene based on their published sequences. The followsity School of Medicine, 660 South Euclid Avenue, St. Louis, MO 63110. E-mail: ing PCR condition was used for each primer set: 95°C for 3 min, followed by [email protected]. 1924 Downloaded from cancerres.aacrjournals.org on June 18, 2017. © 2004 American Association for Cancer Research. Pol IS A CANDIDATE MOUSE LUNG TUMOR MODIFIER GENE 30 cycles of 94°C for 30 s, 55°C for 30 s and 72°C for 1 min, and finally 72°C 0.01% xylene cyanol), heated to 94°C for 3 min, and separated by 12% for 6 min. Annealing temperature was optimized for each primer set. Electro- denaturing PAGE. Gels were quantified by phosphorimage analysis. phoreses on 1.5% agarose gels were performed to resolved PCR products. Human POL Mutation and Expression Analyses. Eleven human lung Genomic DNA- and DNase I-treated cDNA samples were used for those cancer cell lines, including A427 (carcinoma), A549 (carcinoma), CaLu-1 containing only one exon. Amplified PCR products were purified with QIA- (metastatic epidermoid carcinoma), CaLu-3 (adenocarcinoma), CaLu-6 (adequick gel extraction kit (Qiagen, Valencia, CA) and subjected to direct se- nocarcinoma), SK-LU1 (adenocarcinoma), SK-MES1 (squamous cell carciquencing. noma), NCI-H460 (large cell carcinoma), NCI-H596 (adenosquamous carciTo detect alternative transcripts and nucleotide polymorphisms in the Pol noma), NCI-H520 (squamous cell carcinoma), and NCI-H661 (large cell gene, five primer sets were used to cover the entire Pol coding region: primer carcinoma), and the normal fetal lung cells MRC5 [all available from the set 1: forward, 5⬘-GAGGAAGAAGACGCTCCTC-3⬘, and reverse, 5⬘-TTC- American Type Culture Collection, Manassas, VA] were used in this study. CTCCAACAATTCTGTGAC-3⬘; primer set 2: forward, 5⬘-GAGCCGCTA- The cells were grown in Eagle’s MEM ⫹10%FBS (MRC-5, A549, A427, CAGAGAGATG-3⬘, and reverse, 5⬘-GTAGTAAGACCGTCTGCTG-3⬘; CaLu-1, CaLu-3, CaLu-6, SK-LU-1, and SK-MES-1) or RPMI 1640 ⫹ 10FBS primer set 3: forward, 5⬘-GTGGCTCCTAATAAACTCTTG-3⬘, and reverse, (NCI-H460, NCI-H596, NCI-H520, and NCI-H661) and were harvested at 5⬘-AGGCCCTTTCTTAGCACTGC-3⬘; primer set 4: forward, 5⬘-ATGGT- 80 –90% confluence. DNA, RNA, and protein were isolated from these cells by GAACGTGAAGATGCC-3⬘, and reverse, 5⬘-GCCTTGACTCGTTTGCT- standard techniques. Primers used to amplify the human POL gene (GenBank CAT-3⬘; and primer set 5: forward, 5⬘-TCGTGCGGAAAGGACTGTTC-3⬘, accession no. NM_007195) are the following: 1F, 5⬘-GCGACG ACGAGGAAand reverse, 5⬘-ACTAGAATTTCCTTCCTGTGC-3⬘. Alternative mRNA GACG-3⬘ (33-50); 2R, 5⬘-GTATTCCCTTGCTTTTCAGAC-3⬘ (2230-2250); 3F, splicing was detected by using primer sets 1 and 2. 5⬘-GATCTCAGATTGCAGCAGAG-3⬘ (591-610); 4R, 5⬘-AGAAGCCACTCA/J and BALB/cJ GST-Pol Plasmid Constructs. A full length of Pol CAGCACAG-3⬘ (649-667); 5F, 5⬘-GGATTTCCTACCAAGTGGAAG-3⬘ (1447coding sequence was separately amplified using two sets of oligonucleotides: 1467); 6R, 5⬘-GAAGCTGCTTGAAGACTTCTTG-3⬘ (1574-1595); 7F, 5⬘-CAAP1 set: forward, 5⬘-GAACGCGGATCCGCGGCCATGGAGCCCTTGCACGC- GAAGTCTTCAAGCAGCTTC-3⬘ (1574-1595); and 8R, 5⬘-GTCCAATG3⬘(A/J), forward, 5⬘-GAACGCGGATCCGCGGCCATGGAGCCCTCGC- TGGAAATCTGATC-3⬘ (1284-2204). ACGC-3⬘ (BALB/cJ), and reverse, 5⬘-ATAAGGATATCAATCAGGGGAGGCTo examine the 2147 base coding region of the human POL gene for 3⬘; and P2 set: forward, 5⬘-CCTCCCCTGATTGATATCCTTATG-3⬘, and polymorphisms or mutations, we made cDNA from the RNA and amplified reverse, 5⬘-CTCCCTCCATCGATGGACTTATCTGTGCGCCGAGG-3⬘. P1 overlapping regions with primers 1F ⫻ 4R, 3F ⫻ 6R, and 5F ⫻ 2R. After Qiagen and P2 PCR products were digested with BamHI/EcoRV and EcoRV/ClaI PCR purification (Qiagen), the PCR products were both sequenced directly and restriction enzymes. Digested P1 and P2 PCR products were separately cloned cloned using a TOPO-TA PCR cloning kit (Invitrogen). DYE-ET (Amershaminto the pBluesript II SK vector, and their sequences were confirmed by direct Pharmacia, Sunnyvale, CA) and BIG DYE (Applied Biosystems, Foster City, CA) sequencing in both directions. The Pol -pBluesript II SK plasmid containing fluorescent terminator cycle sequencing kits were used. Two to four clones were a full length of Pol open reading frame was produced by subcloning the P2 sequenced in each direction, and direct sequencing of products without cloning in fragment into P1 plasmid. at least two reactions was used to confirm the polymorphisms detected. Western The GST-Pol plasmid was generated by subcloning the ⬃2.2-kb BamHI to blot analysis was performed to examine the protein expression of POL in the ClaI fragment from Pol -pBluesript II SK plasmid into BamHI/ClaI double- human lung cancer cell lines and normal MRC5 line. A polyclonal antibody to the digested glutathione S-transferase (GST)-tagged expression vector pEBG-3X- full-length POL protein made in rabbits was used. Ponceau Red staining was HV. The in-frame open reading frame of GST-Pol fusion was confirmed by used to confirm the even loading of protein. direct sequencing. Purification of GST-Tagged Pol Proteins. The GST-Pol expression Results plasmids were transfected into HEK293 cells using Lipofectamine (Invitrogen, Carlsbad, CA), and 48 h after transfection, cells were lysed in NP40 buffer [20 Expression and Nucleotide Polymorphism Analyses of Genes in mM Tris (pH 7.5), 100 mM NaCl, 1% NP40, 1 mM EDTA, 1 mM DTT, 0.1 mM the Par2 Region. The present minimum Par2 physical region is phenylmethylsulfonyl fluoride, 5 g/ml aprotinin, and 5 g/ml leupeptin]. encompassed by the D18Mit103 and D18Mit188 markers. We obLysates were cleared by centrifugation, and NaCl was added to 1 M before the tained the marker sequence information from the Whitehead Institute/ addition of glutathione-agarose beads and incubation for 2 h. Beads were MIT Center for Genome Research.5 Using the marker sequences to washed by NP40 buffer and eluted in glutathione elution buffer [50 mM Tris blast against the Celera and National Center for Biotechnology Infor(pH 8), 100 mM NaCl, 10 mM glutathione, and 1 mM DTT]. Eluted proteins mation (NCBI) mouse genome databases, we localized these two were resolved by SDS-PAGE to determine purity and concentration. In addition, protein concentrations were estimated by Western blot analysis using markers on both maps. The physical distance between the D18Mit103 human GST-i as a standard. The antibody to full-length human POL was and D18Mit188 markers was ⬃2.4 Mb in the Celera map with both kindly provided by Rajendra Prasad and Samuel H. Wilson. markers located on the scaffold GA_x6K02T2NR3J. In the NCBI Primer Extension Assays. A set of experiments were designed to compare mouse map, these two markers were localized to the contig the incorporation of dATP by the A/J and PALB/c Pol isoforms. The DNA NT_082383 and encompassed a ⬃2.6-Mb region (D18Mit103 at the template used was 5⬘-CTCGTCAGCATCTTCATCATACAGTCAGTG-3⬘. nucleotide position 2932731-2932845 and D18Mit188 at the nucleoThe matched primer was 5⬘-CACTGACTGTATGATGA-3⬘, and the mistide position 5505960-5506058). The chromosome position for each matched primer was 5⬘-CACTGACTGTATGATGG-3⬘. For matched primergene in the candidate region is illustrated in Fig. 1. Generally, the gene template extension, 10, 25, 50, 110, and 225 ng of A/J and BALB/cJ Pol proteins were used. Reactions were performed at 37°C degree for 15 min. For annotations on both maps are consistent to each other. For example, G/T mismatched primer extension, when dATP was added, 100, 200, 300, and four known genes, namely StarD6, Pol , Mbd2, and Dcc, are located in both Par2 regions. Sequence comparison revealed that the 400 ng of A/J and BALB/cJ Pol proteins were used. To examine the abilities of A/J and BALB/cJ Pol proteins to incorporate mCG9249 in the Celera map represents the same gene as the dGTP compared with dATP opposite template T, the primer oligonucleotide 2310002L13Rik does in the NCBI map. Both the mCG9258 and (5⬘-AATTTCTGCAGGTCGACTCCAAAGGCT-3⬘) was 5⬘-end labeled with Loc225699 genes encode a protein similar to 60S ribosomal protein 32 P using T4 polynucleotide kinase and annealed at a 1.5:1 ratio with the L5 and should represent a same gene. However, there are also some template oligonucleotide (5⬘-CCAGCTCGGTACCGGGTTAGCCTTTG- discrepancies between the Celera and NCBI mouse Par2 region. The GAGTCGACCTGCAGAAAT-3⬘). Reactions contained 40 mM Tris-Cl (pH Celera Par2 region has 7 annotated genes, whereas the NCBI Par2 8.0), 30 mM NaCl, 5 mM MgCl2, deoxynucleoside triphosphate (as indicated in region has 11, which may reflect different gene prediction tools and Fig. 3), 10 mM DTT, 1.25% glycerol, 250 g/ml BSA, 2 pmols of primer: template DNA, and 2 ng of GST-Pol . Samples (5 l) were removed at the prediction stringency used by annotators. Another apparent discrepindicated times and added to an equal volume of formamide loading buffer 5 (95% deionized formamide, 25 mM EDTA, 0.01% bromphenol blue, and Internet address: http://www.broad.mit.edu/cgi-bin/mouse/sts_info?database⫽mouse. 1925 Downloaded from cancerres.aacrjournals.org on June 18, 2017. © 2004 American Association for Cancer Research. Pol IS A CANDIDATE MOUSE LUNG TUMOR MODIFIER GENE Fig. 1. Annotated genes in the Par2 candidate region. D18Mit103 and D18Mit188 were separately anchored to Celera (released on August 17, 2003) and National Center for Biotechnology Information (NCBI) Build32 (released on February 10, 2003) mouse genome maps by performing BLASTn search. The unit of gene position is “Mb.” ancy is the position of Mbd2 gene (Fig. 1). For the four known genes, their order in the NCBI mouse genome map is Mbd2-Stard6-Pol -Dcc, which is different from their order (Stard6-Poli-Mbd2-Dcc) in the other three maps, i.e., the NCBI human, Celera mouse, and Celera human genome maps. Because of the high homology between human and mouse Par2 region, the Mbd2 gene apparently has been somehow mistakenly placed during the NCBI sequence assembling. We used reverse transcription-PCR (RT-PCR) and direct sequencing to examine differential expression in lung tissues and coding-region nucleotide polymorphisms for the annotated genes. The result is presented in Table 1. Because the 4930503Rik, Loc383391, Loc383392, and Loc381176 genes were annotated in the Par2 region after this work was submitted, relevant work is still ongoing in our laboratory. A previous study using Northern blot suggested that the Stard6 gene is expressed exclusively in the mouse testis, and its function has been suggested to be specific for fertility (21). However, our RT-PCR results indicate that Stard6 is expressed in mouse lung tissues but has no differential expression or nucleotide polymorphism between A/J and BALB/cJ inbred strains. Our previous study has revealed neither expression difference nor nucleotide polymorphism between A/J and BALB/cJ mice for the Dcc gene (11). Real-time RT-PCR analysis for the Mbd2 gene only revealed a slight expression difference (A/J: BALB/cJ, 0.84 ⫾ 0.03; data not shown), and no nucleotide polymorphism has been found for this gene either. Thus, Stard6, Mbd2, and Dcc are less likely to be the Par2 gene. Two other genes, i.e., A430085C19 and Loc225699, only have one exon and were not detected by DNase I-treated RT-PCR in lung. We could not detect 2310002L13Rik/mCG9249 in either A/J or BALB/cJ lung tissues. Nucleotide Polymorphisms and Alternative mRNA Splicing in the Pol Gene. The remaining known gene in the Par2 region, Pol , has a 2154-bp open reading frame and encodes a 717-amino acid protein. By sequencing its entire coding region, we found a total of 25 nucleotide polymorphisms in the Pol coding region between A/J and BALB/cJ mice. As shown in Fig. 2A, we have identified 10 amino acid-changing polymorphisms and two alternatively spliced exons in Pol between A/J and BALB/cJ mice. Among them, 9 amino acid polymorphisms and 1 alternative splicing variant were consistent with those reported previously (13). The newly observed amino acid changing polymorphism at codon 606 encodes a positively charged arginine (CGA) in BALB/cJ but a neutral Glutamine (CAA) in A/J (Fig. 2B). Pol exon 4a transcript isoform was reported as a product of alternative splicing on exon 4 (13). In our study, we have found that in addition to this isoform (detected by our primer set 2; data not shown), another isoform also exists in mouse lung tissues. The new alternative transcript was detected by primer set 1 and has a shorter nucleotide sequence compared with the regular one (Fig. 2C, a). Directly sequencing this shorter PCR product has revealed that the exon 2 in the full-length Pol mRNA is spliced out without changing open reading frame (Fig. 2C, b). We present this isoform as exon 2d (“d” means “deleted”). In C57BL/6J mice, the exon 2d isoform seems to be more abundant than the regular isoform that contains exon 2, whereas A/J, BALB/cJ, 129/SvJ, and C3H/HeJ lung tissues have more of the regular-length isoform transcript than the exon 2d isoform. We did not observe differential expression of the new exon 2d transcript isoform between A/J and BALB/cJ mice. Initial Biochemical Characterization of Pol Protein. To investigate the properties of the Pol isoforms encoded in A/J and BALB/cJ mice, we expressed and purified both enzymes as full-length GST fusion proteins and measured their polymerization activity. Both enzymes were active in extending a correctly paired primer-template through the addition of dAMP opposite template T (Fig. 3A, a). Thus, the amino acid differences between the two polymerases do not result in loss of polymerization activity by either protein. At concentrations of Pol estimated to be equivalent, more extension of the correctly paired primer was ob- Table 1 Expression and nucleotide polymorphism analyses for genes in the Par2 candidate region Gene ID mCG9249/2310002L13 4930503L19 Stard6 Pol A430085C19 Mbd2 Loc225699/mCG9258 Dcc Loc383391 Loc382292 Loc381176 a Lung expression Description Riken transcript Riken transcript START domain-containing protein 6 DNA polymerase Methyl-CPG binding domain protein Similar to 60S ribosomal protein L5 Tumor suppressor protein Similar to DCC tumor suppressor protein No NDa Yes Yes No Yes No Yes NDa NDa NDa Nucleotide polymorphisms between A/J and BALB/c No Ten amino acid polymorphisms No No No ND, not determined because of recent database update. 1926 Downloaded from cancerres.aacrjournals.org on June 18, 2017. © 2004 American Association for Cancer Research. Pol IS A CANDIDATE MOUSE LUNG TUMOR MODIFIER GENE Fig. 2. Amino acid alterations and transcript isoforms of the mouse Pol gene. A, schematic illustration of amino acid-changing nucleotide polymorphisms and alternative splicing. The full length of Pol mRNA consists of 10 exons (f, E1-E10) with a total of 2497 bp (GenBank accession no. NM_011972). Exon 2d isoform is produced by alternatively splicing out exon 2 (s) without changing the entire open reading frame. The asterisk sign (ⴱ) indicates that the exon 4a isoform has extra 32 bp (䡺) on regular exon 4, which produces a truncated protein caused by an early termination codon (tga) in exon 5. Ten amino acid changing codons are located in exon 1 (2), exon 8 (1), exon 9 (1), and exon 10 (6). The start codon (atg) is at 95 bp position, and the stop codon in the regular isoform is at 2246 bp position. B, amino acid-changing nucleotide polymorphism on codon 606 of the Pol regular transcript. Direct sequencing results revealed that the codon 606 of the Pol full-length transcript encodes a positive-charged arginine (CGA) in BALB/cJ but a neutral glutamine (CAA) in A/J mice. C, alternative mRNA splicing on exon 2. a, reverse transcription-PCR result using primer set 1 (see “Materials and Method” for primer sequences). Two transcript isoforms were detected in A/J and BALB/cJ mouse lung. The longer one is regular Pol transcript with exon 2. The shorter one is a new isoform without exon 2. b, sequencing result revealed that the new Pol isoform is caused by in-frame exon 2 skip. served for the BALB/cJ enzyme than for the A/J enzyme. However, in parallel reactions using somewhat higher enzyme concentrations, a difference between the two isoforms was not apparent for extension of a primer containing a terminal T-G mismatch (Fig. 3A, b). These data suggested that the two isoforms of Pol may differ in their ability to use aberrant substrates. To further test this hypothesis, we examined a property that distinguishes Pol from all other DNA polymerases studied to date—the preferential incorporation of incorrect dGMP over correct dAMP opposite template thymine (14 –17). The results show that both mouse isoforms of Pol do exhibit this noncanonical behavior (Fig. 3B). Thus, when examined at two different concentrations of dGTP or dATP (0.1 and 1.0 mM), incorporation of dGTP is preferred by both enzymes (compare squares to circles). However, at the higher deoxynucleoside triphosphate concentration (black symbols), the A/J Pol prefers dGTP by a factor of 3– 4-fold, whereas the BALB/cJ Pol prefers dGTP by a factor of ⬍2-fold. This observation additionally supports the hypothesis that the amino acid differences between the two mouse isoforms may alter their substrate discrimination properties. Human POL Mutation and Expression in Lung Cancer Cell Lines. To explore the possible role of POL in human lung cancer development, we examined 11 human lung cancer cell lines for mutations in the coding region of the human POL gene. Two silent polymorphisms at codon 12 (TCG to TCT, Ser) and codon 293 (GTG to GTC, Val) were identified in the CaLu-1 cells, and a common polymorphism at position 2180, which changes the amino acid at codon 706 (ACA to GCA, Thr to Ala), was identified in A427, A549, CaLu-3, CaLu-6, NCI-H460, and NCI-H596 cells. These polymorphisms in the lung cancer cell lines all appeared to be heterozygous with the published sequence. Fig. 4A shows a sample without and one with the polymorphism at codon 706. 1927 Downloaded from cancerres.aacrjournals.org on June 18, 2017. © 2004 American Association for Cancer Research. Pol IS A CANDIDATE MOUSE LUNG TUMOR MODIFIER GENE Fig. 3. Primer extension assays. A, differential activities in incorporation of dATP opposite template T at high enzyme concentration. Incorporations of dATP extend matched (a) and G/T mismatched (b) primer-template T. Pol enzymatic activity is reflected by percentage of primers being converted. B, preferential incorporation of dGTP versus dATP opposite template T. Two ng of A/J and BALB/cJ full-length Pol proteins were used in each reaction. At 0.1 and 1 mM deoxynucleoside triphosphate (dNTP) concentrations, both proteins exhibit classical Pol enzymatic property, preferring incorporation of dGTP opposite template T. At 1 mM dNTP concentration, the BALB/cJ Pol protein is less efficient (⬃2-fold) at incorporating dGTP opposite template T than the A/J protein. In addition to the sequence analyses, an assessment of POL protein expression in the human lung cancer cell lines was made. Western analysis demonstrated that POL expression varied among the cell lines from low expression in the normal MRC-5 and the A427, SK-LU-1, and NCI-H460 cancer cells to very high in the CaLu-1 and NCI-H520 cell lines with the other cells in between (Fig. 4B). These expression differences did not correlate with the amino acid change at codon 706 observed in certain cell lines or with the tumor morpho- 1928 Downloaded from cancerres.aacrjournals.org on June 18, 2017. © 2004 American Association for Cancer Research. Pol IS A CANDIDATE MOUSE LUNG TUMOR MODIFIER GENE Fig. 4. Alteration of POL in human cancer cell lines. A, codon 706 polymorphism in human POL gene. Sequencing has been done with reverse primer 2R. ACA to GCA (THR to ALA) was identified in A427, A549, CaLu-3, CaLu-6, NCI-H460, and NCIH596 cells. The polymorphism appeared to be heterozygous with the published sequence as indicated by arrow in Calu-3 sequence. B, Western Blot of human POL protein in lung normal and cancer cell lines. A polyclonal antibody was used to examine protein expression. Ponceau Red staining has been performed to make sure that a similar amount of protein was loaded to each lane. logical subtypes (e.g., adenocarcinoma or squamous cell carcinoma) from which the cells were derived. The protein similarities between the human POL , mouse Pol , and other species such as Arabidopsis thaliana, Caenorhabditis elegans, Escherichia coli, as well as Saccharomyces cerevisiae Pol -like proteins are 76, 29, 29, 32, and 20%, respectively (UniGene).6 Most of conserved amino acids are clustered within the NH2-terminal region, which contains five conserved motifs (22). The evolutionary conservation of the Pol codons was examined using the human, mouse, and fruit fly’s Pol sequences. The fruit fly Pol sequence was derived from the Drosophila melanogaster transcript CG7602-RA (GenBank accession no. AAF54198). We aligned these three sequences using the Clustalw software.7 As shown in Fig. 5, the conserved amino acids are mainly clustered in NH2-terminal region consistent with the previous study (22). The codon 706 shows weak conservation among these three species. At this codon, the fruit fly Pol has a proline, whereas mouse Pol has an alanine. Both are hydrophobic and neutral amino acids. Discussion In this study, we demonstrated the candidacy of Pol for the Par2 locus. Linkage analysis and fine mapping in various mouse crosses and congenic mice have significantly narrowed the Par2 region (7–12). 6 Internet address: http://www.ncbi.nlm.nih.gov/UniGene/clust.cgi?ORG⫽Hs&CID ⫽438533. 7 Internet address: http://www.ebi.ac.uk/clustalw/. Among all of the annotated genes in the Par2 region, Pol was identified as a candidate mouse lung resistance gene based on two lines of evidence: (a) genetic variants were identified between susceptible A/J and resistant BALB/cJ mice, and changes including genetic polymorphisms and altered expression of POL were also observed in human lung cancer cells; (b) primer extension assays with purified BALB/cJ and A/J proteins in vitro found that both forms of Pol are active but that they may differ in substrate discrimination. This result strongly supports the hypothesis that the amino acid differences between the two mouse isoforms may alter their substrate discrimination properties, which may affect the formation of Kras2 mutations in mouse lung tumors. A major characteristic of the highly error-prone human POL is its preference for inserting wobble base G rather than A opposite template T. Primer extension assays demonstrated that the full-length BALB/cJ Pol protein is less efficient than the A/J protein in incorporating G compared with A opposite a template T. At higher concentrations, the full-length BALB/cJ Pol protein incorporates Watson-Crick base A opposite template T more efficiently than the A/J protein. These results are consistent with a genetic modifier role for the Pol variant in mouse and, possibly, human lung cancer susceptibility. Human chromosome 18q21.1 locus is deleted in many human cancers, including squamous cell carcinoma, osteosarcoma, colon cancer, and breast cancer (23–26). Recent studies have indicated that deleted segments of 18q21 contained a lung cancer tumor suppressor gene (27, 28). Because the mouse Par2 region is highly homologous to human chromosome 18p21.1 region, positional cloning of the Par2 gene may facilitate the identification of the human lung cancer suppressor gene. To date, there are three known tumor suppressors (DCC, SMAD2, and SMAD4) located in the human chromosome18q21.1 region, although there is no evidence that these genes play a role in lung cancer. Because the mouse Smad2 and Smad4 genes are located outside of the refined Par2 candidate region, they can be excluded as Par2 candidates. The status of the Dcc gene as a Par2 candidate has been challenged by the fact that neither nucleotide polymorphism nor significant lung expression difference has been found between A/J and BALB/c mice (11). The MBD2 gene encodes methyl-CpG binding proteins that suppress transcription from methylated promoters and is a candidate tumor suppressor. However, one recent mutation study suggests that the MBD2 gene may only have a limited role, if any, in lung cancer tumorigenesis (29). Multiple nucleotide polymorphisms and functional testing results (i.e., different enzymatic activities) provide evidence that the Pol gene is a strong candidate for the mouse Par2 gene. As with tumor suppressors DCC, SMAD2, and SMAD4, the human POL was also mapped to the chromosome 18q21.1 (22). The gene belongs to the Rad30 branch of the recently described UmuC/DinB/Rev1/Rad30 family of DNA polymerases and encodes a 715-amino acid DNA-dependent polymerase POL in human and a 717-amino acid Pol protein in mouse (30). On the basis of in vitro studies, human POL has the lowest fidelity of any eukaryotic polymerase studied to date, which suggests that its activities must be highly specialized. The fact that POL orthologues are evolutionarily conserved in higher eukaryotes from Drosophila to humans also suggests that it provides some selective advantage. Several studies show that the POL gene may play a role in somatic hypermutation (31–33) by which specific mutations occur as part of antibody diversity. Human POL protein has also been shown carrying an intrinsic 5⬘-deoxyribose phosphate lysase activity and can substitute for POL  during BER reactions in vitro (19). Twenty-five nucleotide polymorphisms in the Pol coding region were observed between A/J and BALB/cJ strains that resulted in 10 amino acid alterations. Although none of these amino acid polymorphisms has been located in the conserved enzymatic regions, recent studies have shown that the COOH-terminal region of human POL protein may also have additional critical functions (34 –36). For ex- 1929 Downloaded from cancerres.aacrjournals.org on June 18, 2017. © 2004 American Association for Cancer Research. Pol IS A CANDIDATE MOUSE LUNG TUMOR MODIFIER GENE Fig. 5. Clustalw alignment of human, mouse, and fruit fly Pol proteins. Mouse Pol protein is represented by the A/J sequence. “ⴱ” indicates the identical residues in that column in the alignment.“:” indicates the conserved substitutions. “.” indicates semiconserved substitutions. The codon 706 is highlighted. ample, the motif SRGVLSFF (in which the conserved residues are indicated in bold) is present in residues 540 –547 of human POL and may contribute to PCNA binding (34). Another study has shown that the localization of POL protein in the nucleus requires sequences within amino acids 219 – 451, and sequences within amino acids 492–539 and 636 –715 are critical for interaction between POL and POL proteins (35, 36). The results in Fig. 3 are nonetheless consistent with the possibility that the BALB/cJ and A/J isoforms of Pol differ in substrate discrimination properties. The higher apparent activity for incorporation of dAMP (Fig. 3A) and the lower ratio of dGTP to dATP incorporation (Fig. 3B, 1.0 mM) by the BALB/cJ enzyme are both consistent with the possibility that this enzyme may be more accurate than the A/J isoform, at least for T-dGMP mismatches that would lead to T-A to C-G transition mutations. A more comprehensive test of this hypothesis for this and other mismatches is currently underway. An amino acid polymorphism at the codon 706 of human POL gene was identified in human lung cancer and normal cell lines. It is unclear at this time if this polymorphism will alter its function. The Environmental Genome Project sampled 178 chromosomes during its resequencing of POL and identified A in position 2180 (codon 706) at a proportion of 0.758 and G at 0.242. The estimated heterozygosity was 0.366 for this SNP.8 This frequency is not statistically different from our finding. We also found that the human lung cancer cell lines exhibit varied expression of POL protein, which may suggest a role in the development of lung cancers. Although these expression differences did not correlate with the amino acid change at codon 706 observed in certain cell lines or with the tumor morphological subtypes, it is noteworthy 8 Internet address: http://www.genome.utah.edu/genesnps/cgi-bin/frame.cgi_gene_id⫽350. 1930 Downloaded from cancerres.aacrjournals.org on June 18, 2017. © 2004 American Association for Cancer Research. Pol IS A CANDIDATE MOUSE LUNG TUMOR MODIFIER GENE that there are a number of polymorphisms in the 5⬘-end flanking region of the gene identified by Environmental Genome Project that may affect expression or function. Thus, additional analysis of the POL promoter region should be pursued. The Kras2 gene plays an important role in mouse lung tumor development, with most adenomas and adenocarcinomas containing Kras2 mutations (5, 20). After treatment with urethane, nearly all Kras2 mutations arise in codon 61. Kras2 codon 61 mutations were very frequent (90.9% for CAA3 CGA and 6.1% for CAA3 CTA) in lung tumors following urethane treatment from BALB.B6-Par2 congenic mice and slightly lower (86% for CAA3 CGA) in tumors from BALB/cJ mice (13). After treatment with another carcinogen, diethylnitrosamine, the CAA3 CGA mutation rates in tumors were 46% for parental BALB/cJ mice and 79% for BALB.B6-Par2 congenic mice, respectively (13). It was unclear whether these differences were because of differential protein expression in lungs of BALB/cJ and A/J mice (e.g., parental BALB/cJ mice producing less than half amount of full-length Pol protein as congenic mice) or qualitative (i.e., enzymatic activity) factors. Our primer extension assays present, for the first time, the evidence for the hypothesis that enzymatic activity differences between the BALB/cJ and A/J (or C57BL/6J) Pol proteins may contribute to differences in Kras2 mutation frequency. Indeed, preferential DNA damage and poor repair have been demonstrated to be responsible for the mutation hotspot at codon 12 of Kras gene in human lung cancer (20). The urethaneinduced DNA adduct 1, N6-ethenodeoxyadenosine, has been shown to be a strong mutagenic DNA adduct when replicated in mammalian cells (37). A recent study has revealed that the level of 1,N6-ethenodeoxyadenosine and 3,N4-ethenodeoxycytidine were ⬃70% higher in A/J mice than in C57BL/6J mice (38). Because of the conservation between mouse Pol and human POL proteins, we speculate that mouse Pol proteins are also involved in BER and may affect Kras2 mutation during BER reactions. 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Updated version Cited articles Citing articles E-mail alerts Reprints and Subscriptions Permissions Access the most recent version of this article at: http://cancerres.aacrjournals.org/content/64/6/1924 This article cites 35 articles, 14 of which you can access for free at: http://cancerres.aacrjournals.org/content/64/6/1924.full#ref-list-1 This article has been cited by 11 HighWire-hosted articles. Access the articles at: http://cancerres.aacrjournals.org/content/64/6/1924.full#related-urls Sign up to receive free email-alerts related to this article or journal. To order reprints of this article or to subscribe to the journal, contact the AACR Publications Department at [email protected]. To request permission to re-use all or part of this article, contact the AACR Publications Department at [email protected]. Downloaded from cancerres.aacrjournals.org on June 18, 2017. © 2004 American Association for Cancer Research.