Unit 3 - Transcription (DNA and RNA synthesis) Flashcards

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1
Q

Transcription 3 process

A

1) initiation
2) elongation
3) termination
-occurs in nucleus + DNA is chemically rewritten as an RNA code

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2
Q

simple Initation

A

RNA polymerase binds to the DNA and unwind it

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3
Q

Elongation simple

A

RNA polymerase creat a complementary mRAN strand. it + on ribonucleotides in 5’ to 3’ direction

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4
Q

Termination simple

A

translation ceases, and the mRNA is relesed

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5
Q

STRAND terms

A

template strand = used as a template
coding stand = not used as a template

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6
Q

Initiation in depth

A

RNA polymerase enzyme used to synthesize an RNA stran while using DNA as a template and needs no primer

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7
Q

RNA polymerase

A
  • binds to the promoter region located upstream of the gene
  • and unzips the double strand in order to expose the bases
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8
Q

Promoter

A

a nucleotide sequence that lies just before a gene and allows for the binding of RNA polymerase
- high inn A=T bp
- only two H-bonds = easy to break needing less energy needed

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9
Q

TATA Box

A

a section of DNA with a high % of T and A bases, which recognized by RNA polymerase
Eukaryotes = TATA
Prokaryotes = TATAAT

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10
Q

two steps of initation

A

1) binding to promoter
2) unzipping the DNA

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11
Q

Elongation in depth

A

builds mRNA strand
- incorporates ribonucleotides that r complementary to template DNA (catalyzes the formation of phosphodiester bonds)
- no primer
- 5’ to 3’
- promoter does not get transcribed

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12
Q

where r mRNA found(+)

A

at 3’ end

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13
Q

which enzyme initiates transciption

A

RNA polymerase

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14
Q

RNA is synthesized from strand of DNA

A

DNA template strand

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15
Q

Termination in depth

A
  • The terminator sequence is located at the end of the gene
  • recognizes the terminator sequence (AAUAA) + releases mRNA strand
  • transcription stops (DNA rewinds itself)
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16
Q

After transcription

A
  • mRNA will exit nucleus
  • transcription of mRNA = protein in cytoplasm
17
Q

post transcriptional modification

A
  • newly built mRNA but must be modified bf leaving the nucleus
  • remove non-coding regions
    • Protect the mRNA from cytoplasmic nucleases and phosphates
18
Q

3 modifications

A

1) splicing
2) add 5’ cap
3) add poly-A tail

19
Q

Splicing

A

removal of non coding regions (introns) in the transcript
a) excise the introns
b) ligate exons
c) degraded in the nucleus

20
Q

3 splicing steps

A

1) small nuclear RiboNucleoProteins bond together to from splicesome

2) splicesome loops the intron bringing the exon close together

3) intron is cute and removed

21
Q

5’ cap

A

made of 7-methyl guanosine
- protects mRNA from digestion by enzymes
- ribosomes recognizes this site as initial attachment

22
Q

Poly (A) tail

A
  • 200 A nucleotides r added to 3’ end of mRNA
  • catalyzed by poly-a-polymerase
  • prevent degradation
  • aids in export from nucleus
23
Q

quality control

A
  • no proofreading mechanisms
  • more errors in transcription than replication
  • redundancy of the genetic code
24
Q

first major step in transcription

A

recognition of the promoter sites

25
Q

T or F
during initiation of transcription, RNA polymerase binds to the promoter region

A

T

26
Q

T or F
RNA polymerase transcribes both strands of DNA at the same time

A

F

27
Q

what is added to the 3’ end of mRNA

A

a poly-A-tail