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Central Dogma of Molecular Biology Dr.Aida Fadhel Biawi , October 2013 Enzymes in DNA replication Helicase unwinds parental double helix DNA polymerase III binds nucleotides to form new strands Binding proteins stabilize separate strands Primase adds short primer to template strand DNA polymerase I (Exonuclease) removes RNA primer and inserts the correct bases Ligase joins Okazaki fragments and seals other nicks in sugarphosphate backbone Proofreading and Repairing DNA • DNA polymerases proofread newly made DNA, replacing any incorrect nucleotides 1 A thymine dimer distorts the DNA molecule. 2 A nuclease enzyme cuts the damaged DNA strand at two points and the damaged section is removed. Nuclease DNA polymerase 3 Repair synthesis by a DNA polymerase fills in the missing nucleotides. DNA ligase 4 DNA ligase seals the Free end of the new DNA To the old DNA, making the strand complete. Accuracy of DNA Replication • The chromosome of E. coli bacteria contains about 5 million bases pairs – Capable of copying this DNA in less than an hour • The 46 chromosomes of a human cell contain about 6 BILLION base pairs of DNA!! – Takes a cell a few hours to copy this DNA – With amazing accuracy – an average of 1 per billion nucleotides Protein Synthesis • The information content of DNA is in the form of specific sequences of nucleotides along the DNA strands • The DNA inherited by an organism leads to specific traits by dictating the synthesis of proteins. • The process by which DNA directs protein synthesis, gene expression includes two stages, called transcription and translation. Transcription and Translation • Cells are governed by a cellular chain of command – DNA RNA protein • Transcription – Is the synthesis of RNA under the direction of DNA – Produces messenger RNA (mRNA) • Translation – Is the actual synthesis of a polypeptide, which occurs under the direction of mRNA – Occurs on ribosomes Transcription and Translation • In a eukaryotic cell the nuclear envelope separates transcription from translation • Extensive RNA processing occurs in the nucleus Nuclear envelope DNA TRANSCRIPTION Pre-mRNA RNA PROCESSING mRNA Ribosome TRANSLATION Polypeptide (b) Eukaryotic cell. The nucleus provides a separate compartment for transcription. The original RNA transcript, called pre-mRNA, is processed in various ways before leaving the nucleus as mRNA. Transcription • RNA synthesis – Is catalyzed by RNA polymerase, which Separates the DNA strands and hooks together the RNA nucleotides. – Follows the same base-pairing rules as DNA, except that in RNA, uracil substitutes for thymine RNA • RNA is single stranded, not double stranded like DNA • RNA is short, only 1 gene long, where DNA is very long and contains many genes • RNA uses the sugar ribose instead of deoxyribose in DNA • RNA uses the base uracil (U) instead of thymine (T) in DNA. Synthesis of an RNA Transcript • The stages of transcription are – Initiation – Elongation – Termination Promoter Transcription unit 5 3 3 5 Start point RNA polymerase DNA Initiation. After RNA polymerase binds to the promoter, the DNA strands unwind, and the polymerase initiates RNA synthesis at the start point on the template strand. 1 5 3 Unwound DNA 3 5 Template strand of DNA transcript 2 Elongation. The polymerase moves downstream, unwinding the DNA and elongating the RNA transcript 5 3 . In the wake of transcription, the DNA strands re-form a double helix. Rewound RNA RNA 5 3 3 5 3 5 RNA transcript 3 Termination. Eventually, the RNA transcript is released, and the polymerase detaches from the DNA. 5 3 3 5 5 Completed RNA transcript 3 Synthesis of an RNA Transcript - Initiation • Promoters signal the initiation of RNA synthesis • Transcription factors help eukaryotic RNA polymerase recognize promoter sequences 1 Eukaryotic promoters TRANSCRIPTION DNA RNA PROCESSING Pre-mRNA mRNA TRANSLATION Ribosome Polypeptide Promoter 5 3 3 5 T A T A A AA AT AT T T T TATA box Start point Template DNA strand Several transcription factors 2 Transcription factors 5 3 3 5 3 Additional transcription factors RNA polymerase II 5 3 Transcription factors 3 5 5 RNA transcript Transcription initiation complex • Sense strand, or coding strand, is the segment of double-stranded DNA running from 5' to 3' that is complementary to the antisense strand of DNA, which runs from 3' to 5'. The sense strand is the strand of DNA that has the same sequence as the mRNA, which takes the antisense strand as its template during transcription, and eventually undergoes translation into a protein. Promoter, a regulatory region of DNA usually located upstream of a gene, providing a control point for regulated gene transcription . Synthesis of an RNA Transcript - Elongation • RNA polymerase synthesizes a single strand of RNA against the DNA template strand (anti-sense strand), adding nucleotides to the 3’ end of the RNA chain • As RNA polymerase moves along the DNA it continues to untwist the double helix, exposing about 10 to 20 DNA bases at a time for pairing with RNA nucleotides Non-template strand of DNA Elongation RNA nucleotides RNA polymerase A 3 T C C A A 3 end U 5 A E G C A T A G G T Direction of transcription (“downstream”) 5 Newly made RNA T Template strand of DNA Synthesis of an RNA Transcript - Termination • • Specific sequences in the DNA signal termination of transcription When one of these is encountered by the polymerase, the RNA transcript is released from the DNA. Transcription Overview Post Transcriptional RNA Processing • Most eukaryotic mRNAs aren’t ready to be translated into protein directly after being transcribed from DNA. mRNA requires processing. • Transcription and RNA processing occur in the nucleus. After this, the messenger RNA moves to the cytoplasm for translation. • The cell adds a protective cap to one end, and a tail of A’s to the other end. These both function to protect the RNA from enzymes that would degrade • Most of the genome consists of non-coding regions called introns 1- Non-coding regions may have specific chromosomal functions or have regulatory purposes. 2- Introns also allow for alternative RNA splicing • Thus, an RNA copy of a gene is converted into messenger RNA by doing 2 things: – Add protective bases to the ends – Cut out the introns RNA Processing - Splicing • The original transcript from the DNA is called pre-mRNA. • It contains transcripts of both introns and exons. • The introns are removed by a process called splicing to produce messenger RNA (mRNA) Alteration of mRNA Ends • Each end of a pre-mRNA molecule is modified in a particular way – The 5 end receives a modified nucleotide cap – The 3 end gets a poly-A tail A modified guanine nucleotide added to the 5 end TRANSCRIPTION RNA PROCESSING 50 to 250 adenine nucleotides added to the 3 end DNA Pre-mRNA 5 mRNA Protein-coding segment Polyadenylation signal 3 G P P P AAUAAA AAA…AAA Ribosome TRANSLATION 5 Cap Polypeptide 5 UTR Start codon Stop codon 3 UTR Poly-A tail 1 - Capping - the 5’ end of the pre-mRNA is capped with a 7methyl guanosine nucleotide. Capping is required to: 1- Protect the RNA transcript from degradation 2-Plays an important role in mRNA transport to the cytoplasm 3- Initiation of protein synthesis. CAP 5’ 3 ’ 2- Polyadenylation - the 3’ end of the pre-mRNA is cleaved and a stretch of adenosines are added to the end of the molecule. Use of alternative polyadenylation sites can result in : 1- Insertion or deletion of sequences that control the stability of the mRNA. 2-The polyA tail is also involved in translation termination. CAP 5’ 3’ An 3- Pre-mRNA splicing - intron-exon junctions (also referred to as splice sites) in the pre-mRNA, the intronic sequences are excised and the exons are ligated to generate the spliced mRNA. 5’ CAP An 3’ The enzyme that catalyzes intron excision is a ~ 3 MDa complex spliceosome pre-mRNA spliced mRNA Assembly and structural dynamics of the spliceosome, one of the most complex molecular machines in the cell However, multiple introns may be spliced differently in different circumstances, for example in different tissues. Heart muscle 1 1 2 2 Uterine muscle 5 3 3 1 3 4 4 5 5 Thus one gene can encode more than one protein. The proteins are similar but not identical and may have distinct properties. This is important in complex organisms mRNA Splicing mRNA mRNA Typical human gene structure: 90-95% intron / 5-10% exon average Intron 3500bp / average exon 150 Thus expression of a gene with an intron requires an extra step to remove the intron exon 1 DNA intron GE exon 2 NE transcription pre-mRNA intron RNA splicing mRNA translation protein The human genome sequencing project (Venter et al., 2001) estimated the number of human genes to be between 30,000-40,000, which is much less than the previous estimates . There are 130 thousands types of proteins. Types of RNA Genetic information copied from DNA is transferred to 3 types of RNA: mRNA Copy of information in DNA constitutes ( 2%) , 100,000 KINDS. rRNA Most of the RNA in cells is associated with structures known as ribosomes, the protein factories of the cells.(80%), FEW KINDS It is the site of translation where genetic information brought by mRNA is translated into actual proteins. Types of rRNA : In prokaryotic :( 23S,16S,5S) In Eukaryotic: ( 28S,18S, 5.8S and 5S). Note: S ( Svedberg) is a unit refers to the molecular weight and shape of the compound . tRNA Brings the amino acid to the ribosome that mRNA coded for. (15%), 100 KINDS. It has 4S in molecular weight. Structure of tRNA