* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download OC 28 Nucleic Acids
Amino acid synthesis wikipedia , lookup
Promoter (genetics) wikipedia , lookup
Transcriptional regulation wikipedia , lookup
Silencer (genetics) wikipedia , lookup
Restriction enzyme wikipedia , lookup
DNA sequencing wikipedia , lookup
DNA profiling wikipedia , lookup
Gel electrophoresis wikipedia , lookup
Eukaryotic transcription wikipedia , lookup
Genomic library wikipedia , lookup
Epitranscriptome wikipedia , lookup
Gene expression wikipedia , lookup
Agarose gel electrophoresis wikipedia , lookup
Vectors in gene therapy wikipedia , lookup
Transformation (genetics) wikipedia , lookup
SNP genotyping wikipedia , lookup
Genetic code wikipedia , lookup
Point mutation wikipedia , lookup
Real-time polymerase chain reaction wikipedia , lookup
Molecular cloning wikipedia , lookup
Community fingerprinting wikipedia , lookup
Non-coding DNA wikipedia , lookup
Biochemistry wikipedia , lookup
Bisulfite sequencing wikipedia , lookup
DNA supercoil wikipedia , lookup
Gel electrophoresis of nucleic acids wikipedia , lookup
Artificial gene synthesis wikipedia , lookup
Biosynthesis wikipedia , lookup
28 Organic Chemistry William H. Brown & Christopher S. Foote 28-1 28 Nucleic Acids Chapter 28 28-2 28 Nucleic Acids Nucleic acid: a biopolymer containing three types of monomer units • heterocyclic aromatic amine bases derived from purine and pyrimidine • the monosaccharides D-ribose or 2-deoxy-D-ribose • phosphoric acid Following are names and one-letter abbreviations for the heterocyclic aromatic amine bases most common to nucleic acids 28-3 28 Purine/Pyrimidine Bases O 3 N 2 N 5 HN 6 O 1 6 1 N 2 N O N O H Thymine (T) N H Cytosine (C) O N N N N N H2 7 5 CH3 HN H Uracil (U) Pyrimidine N H2 O 4 N HN 8 N 4 3 Purine N H 9 N N H Adenine (A) H 2N N N H Guanine (G) 28-4 28 Nucleosides Nucleoside: a building block of nucleic acids, consisting of D-ribose or 2-deoxy-D-ribose bonded to a heterocyclic aromatic amine base by a b-glycosidic bond uracil O HN b-D-riboside 1 O N 5' HOCH2 O H H 4' H 2' 3' HO OH Uridine a b-N-glycosidic bond 1' H anomeric carbon 28-5 28 Nucleotides Nucleotide: a nucleoside in which a molecule of phosphoric acid is esterified with an -OH of the monosaccharide, NH2 N O - 5' O P O CH2 - O H N O N N H H H OH OH Adenosine 5'-monophosphate (AMP) 28-6 28 Nucleotides Example 28.1 identify these nucleotides O N H2 N (a) O O O O-P- O-P- O-CH2 O O O H H H HO H N H 2N (b) HOCH2 N N O H H N HN H H O H O P O O- H 28-7 28 Acyclovir & AZT O N HN H2 N N HOCH2 O H H O N H H Acyclovir (drawn to show its structural relationship to 2-deoxyguanosine CH3 HN O HOCH2 H N O H N3 H H H Azidothymidine (AZT) 28-8 28 DNA - 1° Structure Deoxyribonucleic acids (DNA) • a backbone of alternating units of 2-deoxy-D-ribose and phosphate in which the 3’-OH of one 2-deoxy-Dribose is joined by a phosphodiester bond to the 5’OH of another 2-deoxy-D-ribose unit Primary Structure: the sequence of bases along the pentose-phosphodiester backbone of a DNA molecule (or an RNA molecule) • read from the 5’ end to the 3’ end 28-9 28 DNA - 1° Structure O phosphorylated 5' end O - CH3 HN 5' O O-P- O-C H2 O H H N O O O= P O Ofree 3' end H O H N NH H CH2 H N O N H2 H H H 3' OH N H 28-10 28 DNA - 2° Structure Secondary structure: the ordered arrangement of nucleic acid strands The double helix model of DNA 2° structure was proposed by James Watson and Francis Crick in 1953 Double helix: a type of 2° structure of DNA molecules in which two antiparallel polynucleotide strands are coiled in a righthanded manner about the same axis 28-11 28 T-A Base Pairing A major factor stabilizing the double helix 28-12 28 C-G Base Pairing 28-13 28 Forms of DNA B-DNA • • • • the predominant form in dilute aqueous solution a right-handed helix 2000 pm thick with 3400 pm per ten base pairs minor groove of 1200pm and major groove of 2200 pm A-DNA • a right-handed helix, but thicker than B-DNA • 2900 pm per 10 base pairs Z-DNA • a left-handed double helix 28-14 28 DNA - 3° Structure Tertiary structure: the three-dimensional arrangement of all atoms of nucleic acid, commonly referred as supercoiling Circular DNA: a type of double-stranded DNA in which the 5’ and 3’ ends of each stand are joined by phosphodiester bonds (Fig 28.10) Histone: a protein, particularly rich in the basic amino acids lysine and arginine, that is found associated with DNA molecules 28-15 28 DNA - 3° Structure Chromatin: consists of DNA molecules wound around particles of histones in a beadlike structure • further coiling produces the dense chromatin found in nuclei of plant and animal cells 28-16 28 Ribonucleic Acids (RNA) RNA are similar to DNA in that they, too, consist of long, unbranched chains of nucleotides joined by phosphodiester groups between the 3’-OH of one pentose and the 5’-OH of the next. However, • the pentose unit in RNA is b-D-ribose rather than b2-deoxy-D-ribose • the pyrimidine bases in RNA are uracil and cytosine rather than thymine and cytosine • RNA is single stranded rather than double stranded 28-17 28 RNA RNA molecules are classified according to their structure and function Type Molecular Weight Range (g/mol) mRNA tRNA rRNA 25,000 - 1,000,000 23,000 - 30,000 35,000 - 1,100,000 Number of Percentage Nucleotides of Cell RNA 75 - 3,000 73 - 94 120 - 2904 2 16 82 Ribosomal RNA (rRNA): a ribonucleic acid found in ribosomes, the site of protein synthesis 28-18 28 RNA Transfer RNA (tRNA) : a ribonucleic acid that carries a specific amino acid to the site of protein synthesis on ribosomes O t RNA -O- P-O- CH 2 O amino acid, bound as an ester to its specific tRNA - H H O O Base H H OH C= O C N H3 + H R 28-19 28 RNA Messenger RNA (mRNA): a ribonucleic acid that carries coded genetic information from DNA to the ribosomes for the synthesis of proteins • present in cells in relatively small amounts and very short-lived • single stranded • their synthesis is directed by information encoded on DNA • a complementary strand of mRNA is synthesized along one strand of an unwound DNA, starting from the 3’ end 28-20 28 RNA • the synthesis of mRNA from DNA is called transcription DNA template 3'-A-G-C-C-A-T-G-T-G-A-C-C-5' 5'-U-C-G-G-U-A-C-A-C-U-G-G-3' mRNA 28-21 28 The Genetic Code U C U UUU Phe UUC Phe UUA Leu UUG Leu C UCU Ser UCC Ser UCA Ser UCG Ser A UAU UAC UAA UAG CUU Leu CUC Leu CUA Leu CUG Leu CCU Pro CCC Pro CCA Pro CCG Pro CAU His CAC His CAA Gln CAG Gln CGU Arg CGC Arg CGA Arg CGG Arg U C A G Ile Ile Ile Met ACU Thr ACC Thr ACA Thr ACG Thr AAU Asn AAC Asn AAA Lys AAG Lys AGU Ser AGC Ser AGA Arg AGG Arg U C A G GUU Val GUC Val GUA Val GUG Val GCU Ala GCC Ala GCA Ala GCG Ala GAU Asp GAC Asp GAA Glu GAG Glu GGU GGC GGA GGG U C A G AUU A AUC AUA AUG* G G Tyr UGU Cys Tyr UGC Cys Stop UGA Stop Stop UGG Trp *AUG also serves as the principal initiation codon. Gly Gly Gly Gly U C A G 28-22 28 The Genetic Code Properties of the Code • only 61 triplets code for amino acids; the remaining 3 (UAA, UAG, and UGA) signal chain termination • the code is degenerate, which means that several amino acids are coded for by more than one triplet. Leu, Ser, and Arg, for example, are each coded for by six triplets • for the 15 amino acids coded for by 2, 3, or 4 triplets, it is only the third letter of the codon that varies. Gly, for example, is coded for by GGA, GGG, GGC, and GGU • there is no ambiguity in the code; each triplet codes for one and only one amino acid 28-23 28 Sequencing DNA Restriction endonuclease: an enzyme that catalyzes hydrolysis of a particular phosphodiester bond within a DNA strand • over 1000 endonucleases have been isolated and their specificities determined • typically they recognize a set sequence of nucleotides and cleave the DNA at or near that particular sequence • EcoRI from E. coli, for example, cleaves as shown cleavage here 5' G- A- A -T -T - C- - -3 ' EcoRI 5' G + 5 ' -A - A- T -T -C- -- 3 ' 28-24 28 Sequencing DNA • following are several more examples of endonucleases and their specificities Recognition Enzyme Sequence AluI AG CT BalI TGG CCA Recognition Enzyme Sequence HpaII C CGG Mbol GATC FnuDII CG CG Not I GC GGCCGC HeaIII GG CC SacI GAGCT C 28-25 28 Sequencing DNA Polyacrylamide gel electrophoresis: a technique so sensitive that it is possible to separate nucleic acid fragments differing from one another in only a single nucleotide • Maxam-Gilbert method: a method developed by Allan Maxam and Walter Gilbert; depends on base-specific chemical cleavage • Dideoxy chain termination method: developed by Frederick Sanger • Gilbert and Sanger shared the 1980 Nobel prize for biochemistry for their “development of chemical and biochemical analysis of DNA structure.” 28-26 28 Replication in Vitro • During replication, the sequence of nucleotides in one strand is copied as a complementary strand to form the second strand of a double-stranded DNA • Synthesis is catalyzed by DNA polymerase • DNA polymerase will catalyze synthesis in vitro using single-stranded DNA as a template, provided that (1) the four deoxynucleotide triphosphate (dNTP) monomers and (2) a primer are present • Primer: an oligonucleotide capable of forming a short section of double-stranded DNA (dsDNA) by basepairing with its complement on a single-stranded DNA (ssDNA) 28-27 28 Replication in Vitro • Because a new DNA strand grows from its 5' to 3' end, the primer must have a free 3'-OH group to which the first nucleotide of the growing chain is added 5' T C A A Single-stranded DNA C G A T C G dATP, dTTP, dCTP, dGTP 3' HO direction of synthesis catalyzed by DNA polymerase T G A C Primer A T OH 3' 5' 28-28 28 Dideoxy Chain Termination • the key to the chain termination method is addition to the synthesizing medium of a 2’,3’-dideoxynucleotide triphosphate (ddNTP) • because a ddNTP has no 3’-OH, chain synthesis is terminated where a ddNTP becomes incorporated O O O O- P-O- P-O- P-O-CH 2 O- O- OH Base O H H H H H A 2',3'-dideoxynucleoside triphosphate (ddNTP) 28-29 28 Dideoxy Chain Termination In this method, the following are mixed • single-stranded DNA of unknown sequence and primer; then divided into four reaction mixtures To each reaction mixture is then added • the four dNTP, one of which is labeled in the 5’ end with phosphorus-32 32 15P 32 16S + Beta particle + Gamma rays • DNA polymerase • one of the four ddNTPs 28-30 28 Dideoxy Chain Termination after gel electrophoresis of each reaction mixture • a piece of film is placed over the gel • gamma rays released by P-32 darken the film and create a pattern of the resolved oligonucleotide • the base sequence of the complement to the original strand is read directly from bottom to top of the developed film 28-31 28 Dideoxy Chain Termination Polyacrylamide gel electrophoresis A G Larger fragments C T 3' A G T T G This sequence is the complement of the DNA template C T Smaller fragments If the complement of the DNA template is Then the original DNA template must be A 5' 5 ' -A -T - C-G- T- T -G- A -3 ' 5 ' -T -C- A -A -C- G-A - T- 3 ' 28-32 28 Prob 28.8 Draw structural formulas for the enethiol (the sulfur equivalent of an enol) forms of each antimetabolite used in the treatment of certain types of cancer. S S HN 6 N N N H 6-Mercaptopurine HN H2 N 6 N N N H 6-Thioguanine 28-33 28 Prob 28.9 Draw two additional tautomers for cytosine and three additional tautomers for thymine. N H2 N O O CH3 HN N H Cytosine (C) O N H Thymine (T) 28-34 28 Nucleic Acids End Chapter 28 28-35