Central Dogma Of Molecular Biology PDF
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Musni, Pauleen Frances M.
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Summary
This document provides an overview of the central dogma of molecular biology, including the processes of DNA replication, transcription, and translation. It also discusses genes, simple and complex organisms, and RNA Polymerase, and their functions.
Full Transcript
CENTRAL DOGMA GENES - nucleotide sequences that carry of molecular biology specific instructions for the cell - The smallest hereditary unit that Central dogma of molecular...
CENTRAL DOGMA GENES - nucleotide sequences that carry of molecular biology specific instructions for the cell - The smallest hereditary unit that Central dogma of molecular biology can be passed from parent to - Process of making copies of offspring genetic information - Process of conversion into protein Note: number and structure of gene products DEPENDS per species - DNA can be replicated and converted to RNA and then into Gene expression - process of converting proteins in this information into genes into a functional protein product DNA: stored in the nucleus - Replicates after each cell division Simple organisms - more segments/genes DNA gets transcribed into RNA, - Prokaryotic RNA gets translated into protein - Es: bacteria, archaea - Tightly packed DNA with genes DNA - goes through transcription RNA- goes through Translation Note: prokaryotes or a simple organisms because there only a little can fit inside Proteins - is the final product them unlike humans - These are enzymes, antibodies Note: Eukaryotes like human have more Reverse transcription non coding material known as “introns” - Is an exception which are the gray area - Only for viruses, they process RNA to become DNA More complex organisms = more - Only exhibited by retroviruses non-coding regions Retroviruses example: Human Organism: Chromosomal segment immunodeficiency virus (HIV) Bacteria: 20kb Yeast: 20kb Drosophila: 200kb Note: All HUMAN cells , even a part of Human: 200kb human cell (like hand cells, thigh cells, etc.) are eukaryotes PROKARYOTES - the entire gene codes for a protein or molecule Musni, Pauleen Frances M. I BSN I biochem reviewer EUKARYOTES - the gene consists of Mini- satellites & Microsatellites coding and non-coding regions - Shorter repeats INNON, EXCO - Repeated in the entire genome INTRONS - non-coding region - Used to monitor mutations - Nascent mRNA - undergo RNA implicated diseases like Cancer splicing - Remains inside the nucleus Additional: - Note part of the mature RNA Genome - entirety of genetic material - removed during transcription Gene - specific segment EXONS- coding region DNA REPLICATION - The one translate in for protein synthesis REPLICATION - process by which DNA - Mature RNA/ expressed/ exits the makes copies of itself nucleus - Occurs in semi-conservative - Joined together in transcription to manner form FINAL mRNA product through - Takes place in NUCLEUS of RNA Splicing Eukaryotic cells, and CYTOPLASM of prokaryotic cells SPLICING - process of intron removal and exon joining Semi- conservative - one strand of the parent DNA becomes the template for Mature RNA only has exons the daughter strands - When two strands separate they Note: Only 3% of human DNA codes for become the template proteins Other models: Conservative model & Additional: Dispersive model Maintenance of chromosomal structure: ORIGIN OF REPLICATION - Replication starts here Disease susceptibility Where the double stranded DNA Gene expression (dsDNA) begins to open to form the SATELLITES - highly repetitive “REPLICATION BUBBLE” - A chromosome can have multiple - Is a Non coding DNA sequence origins - Provide structural stability to - Eukar: multiple origin, Prokar: one chromosomes origin Has 2 kind: mini-satellites, microsatellites Musni, Pauleen Frances M. I BSN I biochem reviewer REPLICATION FORK - where replication Additional: oligonucleotide - actively occurs polynucleotide molecules that contain small number of nucleotides REPLISOME - assembly of proteins that facilitate DNA replication at the CLAMP PROTEIN replication fork - Keeps DNA polymerase in place - All proteins, enzymes, molecules DNA POLYMERASE (DNA Pol) COMPONENTS OF REPLISOME: - Synthesizes new DNA strand GHP-CPL-SSB - Can only add to existing - DNA Gyrase/ Topoisomerase nucleotide chain and cannot - Helicase initiate replication - Primase - Clamp protein DNA LIGASE - DNA Polymerase (DNA Pol) - Joins OKAZAKI FRAGMENTS in the - DNA Ligase lagging strand - Single- stranded Binding Proteins Okazaki fragments - short DNA regions (SSB) that is replicated DNA GYRASE/ TOPOISOMERASE SINGLE-STRANDED BINDING PROTEINS - prevents DNA from supercoiling (SSB) - Prevents by introducing breaks to - Stabilizes and protects the single relieve stress stranded region of DNA during HELICASE replication - breaks the H-bonds between base pairs to unzip the dsDNA LEADING VS LAGGING STRANDS - Separate bonds Where does replication occur? PRIMASE - It occurs on both strands of the - Synthesize primers for DNA DNA on both sides of DNA polymerase replication bubble - PRIMER - initiates replication The newly synthesized DNA is called Note: without the primer made by the either leading strand or lagging strand primase DNA polymerase cannot start replication Leading strand - 3 - Synthesized using the template Note: DNA polymerase follow the primer 3’to 5 towards the replication fork - Replication is continuous Musni, Pauleen Frances M. I BSN I biochem reviewer Lagging strand - 5 - Synthesized using template 5’to 3’ What should happen for transcription to towards replication fork take place? - Replication is discontinuous - DNA must be unwind and - Forms Okazaki fragments that separated by proteins are joined together at the end Transcription bubble - opening in the Why does leading and lagging strand double helix where transcription takes happen? place - Because of the DNA polymerase - DNA polymerase can only Separated DNA strands: synthesize 5’to 3 direction - Template strand - Coding strand Lagging strand - goes against fork movement, discontinuos, 5’to 3’’ Template Strand - DNA strand that is transcribed Leading strand - goes with the fork - Also called the negative strand or movement, continuous, 3’to 5’ antisense strand Coding strand - DNA strand that is NOT DNA REPLICATION IN BRIEF transcribe 1. Opening of the DNA - Called the positive strand or sense superstructure strand 2. DNA relaxation via DNA gyrase 3. DNA unwinding via helicase RNA POLYMERASE 4. Primer synthesis bia primase - Enzyme responsible for RNA 5. DNA elongation via DNA synthesis polymerase - Reads template from 3’ to 5 6. DNA ligation via DNA ligase - Synthesizes RNA from 5’ to 3’ - RNAPol II is used for mRNA RNA TRANSCRIPTION - Cannot recognize genes on their own Transcription - process through which - Need help of transcription factors genetic information from DNA is converted into mRNA in the nucleus TRANSCRIPTION UNIT - First step of gene expression - Protein-gene - Can be divided into: Regulatory Transcript - resulting mRNA molecule regions & structural gene Musni, Pauleen Frances M. I BSN I biochem reviewer Promoter region 2. Elongation - addition of the - Located upstream, (before the appropriate complementary nucleotide to transcription site) the growing transcript - Identifies which DNA strand is the template 3. Termination - release of the complete - Initial binding site of transcription but non- functional transcript call the factors pre-mRNA upon transcription of the - call RNA polymerase for binding terminator region - Note: transcription factors - give signal to 4. Post-transcriptional modifications - where RNA polymerase binds processing of pre-mRNA into functional mature mRNA PROMOTER REGION - Consensus Sequence - Initiation signal Consensus sequence - identifies the precise nucleotide at which transcription begins - Where initial transcription factors binds - EX: TATA box Initial signal - gives RNA pol the signal when to start transcription TERMINATION REGION - Nucleotides at the end of a gene that signals RNA polymerase to end transcription - - ends transcription process RNA TRANSCRIPTION IN BRIEF 1. Initiation - binding of transcription and RNA polymerase to the promoter region Musni, Pauleen Frances M. I BSN I biochem reviewer