Chapter 13 Flashcards

(51 cards)

1
Q

Each structural gene has

A

its own promoter, and is transcribed separately. they dont have polycistronic rna.
so its promoter, gene, promoter, gene.

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2
Q

in multicellular organisms

A

only a small fraction of the genes are expressed.

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3
Q

Developmental and homeostasis

A

maintain same number of cells

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4
Q

enhancers are both

A

positive and negative (repress the gene).

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5
Q

enhancers

A

distance from the gene. dna loop formation brings the sequences together. 50kb from the promoter.

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6
Q

cis acting regulatory sequences

A

regulate transcription located on same chromosome that regulatory sequence is on.

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7
Q

trans acting regulatory proteins

A

proteins able to identify regulatory sequences on any chromosome.

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8
Q

enhanceosome

A

proteins bind other proteins to form large protein complex

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9
Q

pioneer factors

A

they bind first, which allows binding of other transcription factors.

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10
Q

mutation in enhancer module

A

can cause abnormal expression.

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11
Q

locus control region LCR

A

regulates transcription of linked genes at distal chromatin sites. regulates 6 genes. contains 4 regulatory sequences, hs1 to hs4

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12
Q

the hs1 to hs4 make small dna loops that serve as

A

a bridge to the promoters of the b globin complex

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13
Q

the making of galactose

A

requires the action of products of each of four galactose-utilization (GAL) genes

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14
Q

upstream activator sequence (UAS) in yeast

A

transcription activator protein that binds to enhancer element. binding sites for gal4.

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15
Q

when galactose is absent

A

gal80 binds to gal4, blocks gal gene transcription.

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16
Q

when galactose is present

A

gal3 binds gal80, so this way it doesn’t bind to gal4. then gal4 initiates gal gene transcription.

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17
Q

mediator

A

enhancesome that forms after gal4 binds uas. creates dna loop to regulate transcription.

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18
Q

transcription repression Mig1

A

bw uas and Gal1. When there is glucose, Mig1 is produced. Mig1 attracts Tup1, and repress transcription. (prevents uas from starting transcription)

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19
Q

insulator

A

enhancer action on specific gene and away from nearby genes that are not to be regulated by that enhancer.

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20
Q

repression dominant over activation

A

true

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21
Q

constitutive heterochromatic

A

always heterochromatic (tightly compacted)

22
Q

facultative heterochromatin

A

bw being heterochromatic and euchromatic

23
Q

E(var) mutations

A

(enhancers of position effect variegation). mutation encourages heterochromatin formation, increase appearance of mutant white eye phenotype.

24
Q

Su(var) mutations

A

(suppressors of position effect variegation). block heterochromatin formation, increase appearance of normal eyes.

25
length of promoters
1-2 kb long.
26
if you have mutations in the sonic hedgehog (SHH),
you will have multiple fingers.
27
how do activator and repressor bind to regulatory dna if its packed into chromatin
some regulatory sequences are not tightly bound by histones, so more access. 2: chromatin remodelers. 3: chromatin modifiers.
28
open promoters
associated with active genes, like housekeeper genes.
29
nucleosome depleted region (ndr)
100-150 bp region, adenine and thymine rich (poly A/T tract), no TATA box.
30
open chromatin
regulatory sequences access regulatory proteins. DNase I cuts DNA in open chromatin regions, but cant cut in closed chromatin regions. (tells biologists whether a region is open or closed.)
31
chemical modifiers
add or remove chemical groups to modify histone proteins.
32
histone acetyltransferases (HATs)
writers that add acetyl groups
33
histone deacetylases (HDACs)
removes acetyl groups
34
histone methyltransferases (HMTs)
writers that add methyl groups
35
histone demethylases (HDMTs)
remove methyl groups
36
methylation can play a role in
converting open euchromatin to closed heterochromatin, just like deacetylation.
37
if chromatin is in an inaccessible heterochromatic state, how do factors bind to its dna to initiate the transition to euchromatin?
by pioneer factors, which access dna even in heterochromatin.
38
PcG
acting in gene repression
39
Trx
maintain gene expression, opposite to the activity of PcG complex.
40
epigenetic
heritable changes in gene expression but no change in dna sequence. changes by maternal behavior (licking example, more happier dogs).
41
most epigenetic marks are erased during
meiosis, yet it can be passed unto another generation.
42
long noncoding rnas (lncRNAs)
long rnas without an open reading frame.
43
X inactivation
one active euchromatic X chromosome, one inactive heterochromatic X chromosome (mostly silent)
44
Xist gene
active on heterochromatic X, inactive on euchromatic X. it is a lncRNA, and is expressed in cells with at least 2 X's. randomly inactivate 1 of 2 X's to form Barr-bodies
45
genomic imprinting
both copies of genes are functional, just one is expressed. (can be from mother or father.)
46
imprinting control region ICR
bw H19 and IGF2
47
Dicer
cuts dsRNA into 21-25 bp
48
siRNA or miRNA is processed by
RISC (RNA-Induced Silencing Complex). RISC contains Argonaute that produce guide RNA (single stranded). the other is denatured.
49
when good rna goes bad sense rna antisense rna double stranded rna
no effect on offspring no effect twitching
50
When complementarity is perfect: | When complementarity is imperfect:
target mrna is degraded | target mrna is repressed.
51
when bees are injected w rnai
queens pop is lowered. # of dna methylases: lower amounts of dna methylase 3.