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Gene expression

HBIO3 unit 8

QuestionAnswer
What did Fredrick Griffith find he found that there was something that transformed a non-virulent strain of bacteria to a virulent strain in 1928
What did Griffith's experiment use he used a smooth strain (s) with a protective capsule that kills mice, and a rough strain (r) that has no capsule so it doesn't affect mice
What happened in Griffith's experiment He heat-killed the smooth strain which didn't affect the mice but when he mixed that with the rough strain, it was turned into living smooth strain
What did Oswald Avery find He found that DNA was the transforming factor, but didn't understand how - 1944
What happened in Avery's experiment He mixed killed smooth strain and living rough strain bacteria with enzymes and found when DNAse is present, the mice live
What did Hershey and Chase do They tracked DNA and PRO and found that DNA was being copied not PRO
What did Hershey and Chase's experiment use -Bacteriophage (virus that infects bacteria) -Ratiolabelled phoshorus (found in DNA) -Ratiolabelled sulfur (found in PRO)
What happened in Hershey and Chase's experiment The virus injected it's DNA into the bacterium, who's DNA was then transformed into the viruses, meaning phosphorus was found in the bacterium, not sulfur
The chemical formula for Deoxyribose and Phosphate group is C5H10O4 and Po4-
The nitrogen bases are Adenine (A), Guanine (G), Cytosine (C), and Thymine (T)
Purines are Adenine and Guanine - doubled ringed and larger
Pyrimidines are Cytosine and Thymine - single ringed
The base pairs are -Guanine and Cytosine (3 H+ bonds) -Adenine and Thymine (2 H+ bonds)
DNA replication -happens during s phase in the nucleus -is a semiconservative process -requires multiple enz
Helicase cuts H+ bonds and unwinds DNA creating the replication fork
Single-stranded binding (SSB) protein prevent strands from reattaching
Primase lays down RNA primers for polymerase
DNA Polymerase Adds new bases in the 3'->5' direction and replaces RNA primers with correct nucleotides
Topoisomerase prevents overwinding ahead of replication fork
Okazaki fragments pieces/sections of newly made lagging strand
DNA Polymerase 𝝳 and 𝜶 - 𝝳 adds new bases and checks for errors and - 𝜶 adds bases where RNA primers were
Protein synthesis is A process in which cells make proteins
Transcription is making mRNA from DNA in the nucleus
Transcription first 2 steps 1) DNA is unwound and the strands are separated 2) RNA polymerase used the template strand containing the gene to form the mRNAi
Transcription last 2 steps 3) the iotrons are removed from the mRNAi and the exons are spliced together to from the mRNAm 4) The mRNAm leaves the nucleus through the nucleus poles
Translation happens in the cytoplasm
Translation first 2 steps 1) 2 ribosomal subunits "sandwich" the mRNAm and move the start codon (AUG) into the reading window 2) the 1st tRNA with the anticodon that is complementary to the start will enter the A site of the reading window
Translation last 2 steps 3) The mRNAm will shift in the reading window and the new tRNA will arrive at A site peptide bonds will continue to form between adjacent Aa's 4) When a stop codon enters the reading window the ribosome will release the mRNAm
The 2 steps of protein synthesis is 1) Transcription 2)Translation
The 3 types of RNA are 1) Messenger - mRNA 2) Ribosomal - rRNA 3) Transfer - tRNA
Differences between DNA and RNA 1) DNA has 2 strands - RNA has 1 strand 2) DNA has deoxyribose sugar - RNA has ribose sugar 3) DNA has thymine (T) - RNA has uracil (U)
mRNA is -made from DNA template during transcription -carries instructions from the nucleus to the cytoplasm for -2 forms: mRNAi (made of introns + exons) and mRNAm (only exons)
rRNA is -RNA part of a ribosome -Reads mRNA codons and attaches Aa together
A ribosome is made of Protein and rRNA
tRNA is -carries specific Aa -has an anticodon on bottom (matches with codon)
Created by: erica.y
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