Lecture 4 Dr. Williams Flashcards

Gene Expression II: Transcriptional Regulation

1
Q

Importance of TBP?

A

Allows for precision binding of the transcription machinary

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2
Q

How does the pre-initiation complex form?

A

Binding of TFIID, followed by assembly of multi-protein complex that eventually includes polymerase

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3
Q

How many subunits does RNA Pol II have?

A

12 subunits

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4
Q

Protein binding can alter?

A

Transcription rates: positive or negative

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5
Q

Lac Operon low lactose:

A

Lac repressor binds tightly t o lac operator and block RNA pol access to promotor

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6
Q

Lac Operon elevated lactose:

A

low levels of beta-galactosidase activity results in formation of allolactase

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7
Q

Define: Dyad Symmetry

A

Palindromic sequence that may indicate a protein complex with two identical subunits

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8
Q

Define: DNA Binding Domains

A

contain discrete domains that specifically interact with unique DNA elements. Organized into families based on conserved BDBs.

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9
Q

Most common DBD in bacteria?

A

Helix-Turn-Helix motif

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10
Q

Helix-Turn-Helix

A

fits into the major groove of DNA, and recognizes something

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11
Q

Name 3 DBDs utilized in eukaryotic DNA binding proteins:

A

Zinc Finger
Basic region-leucine zipper
Basic region-helix-loop-helix

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12
Q

Zinc Finger

A

zinc atom interacts with major groove

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13
Q

Describe function of: CRP-cAMP complex

A

Proteins that make direct contact with RNA polymerase, and makes it more likely to unwind DNA and initiate transcription

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14
Q

Define: Chromatin

A

The state in which DNA is tightly bound by histones and is unavailable for transcription

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15
Q

How to remodel chromatin?

A

modification DNA by methylation
modification of histones (Acetylation, ubiquitylation, SUMOylation, methylation)
Rearranging nucleosomes

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16
Q

Where does DNA methylation occur?

A

C5 of Cytosine in a CpG dinucleotide

17
Q

What is SWI-SNF remodeling comples?

A

A multisubunit that destabilizes the chromatin structure and gives transcription machinery access to the promotor. Uses ATP hydrolysis to alter nucleosome positioning

18
Q

Fragile X Syndrome

A

X-linked recessive neurological disorder caused by mutations in the FMR1 gene that codes the FMRP protein, a RNA binding protein that plays a role in translation regulation. This mutational event is an expansion of the CGG triplet expansion diseases.

19
Q

Define: Genomic Imprinting

A

Somatic cells that have methylated alleles from either parent

20
Q

Angelman Syndrome

A

Maternal SNRNPN and UB3A is missing, paternal UB3A is imprinted “off” leading to severe intellectual disabilities, and developmental delay. Happy demeanor, and microcephaly, possibly with seizures

21
Q

Prader-Willi Syndrome

A

Paternal SNRNPN and UB3A are missing, and maternal SNRNPN is imprinted “off”, resulting in initial failure to thrive, later increased interest in food, and mild intellectual disabilities, and possibly behavior issues

22
Q

Define: SNRNPN

A

Small nuclear ribonucleoprotein