Gene Regulation Flashcards

1
Q

production of enzymes is regulated by

A

feedback inhibition or gene regulation
ex. operon model in bacteria

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2
Q

operator

A

segment of DNA in bacteria that can act as an on/off switch for a cluster of related genes

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3
Q

operon

A

stretch of DNA including promoter, operator, and genes

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4
Q

repressor

A

product of a regulatory gene which can bind operator and switch transcription off (repress it)
can be active or inactive, depending on corepressor

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5
Q

repressible vs inducible operon

A

repressible - operon is usually on, binding of repressor turns transcription off
ex. trp operon

inducible - operon is usually off, binding of inducer inactivates repressor and switches transcription on
ex. lac operon

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6
Q

positive control

A

uses stimulatory protein
can increase synthesis of a product that is already being synthesized

ex. CAP - catabolite activating protein
CAP activated by cAMP binds to promoter to increase RNA pol II binding and increase rate of synthesis

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7
Q

differences in cell type result from

A

differential gene expression because all cells share same genome

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8
Q

how histone modification affects gene expression

examples

A

genes with packed heterochromatin not usually expressed
modifications influence chromatin structure and expression

acetylation - to lysine residues, opens chromatin structure, promoting transcription initiation
methylation - causes condensing of chromatin
phosphorylation - next to methylated AA can loosen chromatin

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9
Q

DNA methylation can cause

A

long term silencing of genes due to condensation of chromatin structure
genomic imprinting - methylation of either parent’s alleles of a gene can be passed down to future generations of cells
genomic imprinting is type of epigenetic inheritance

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10
Q

high level of transcription in eukaryotes depends on

A

control element associated with genes and specific transcription factors interacting

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11
Q

control elements function and types

A

segments of non-coding DNA where transcription factors bind

proximal control elements - located close to promoter
distal control elements/enhancers - far away or on intron
(whole region is enhancer, control elements are individual sequences of which there can be multiple)

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12
Q

activator in eukaryotic transcription

A

binds to enhancer and stimulates transcription
domains: DNA-binding and transcription activating
can facilitate protein-protein interactions, or influence chromatin structure
some can be repressors instead

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13
Q

co-expressed eukaryotic genes

A

have same combo of control elements even if they are scattered across separate chromosomes

particular combo of control elements with right activator proteins can activate transcription when appropriate

Depending on cell, and required proteins, TF factors present will be tailored to required proteins to be transcribed

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14
Q

is chromatin static in the nucleus?

A

no, it can move towards “hot spots” with higher transcription material availabilities
chromatin produces loops towards hot spots for transcriptions

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15
Q

types of post-transcriptional regulation

A
  1. alternative splicing
  2. blockage of translation initiation by regulatory proteins binding to 5’ end of mRNA
  3. Nucleotide sequences in 3’ UTR which dictate lifespan in cytosol
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16
Q

which mRNA (eukaryotic vs prokaryotic) is longer lived?

A

eukaryotic mRNA

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17
Q

Noncoding RNA regulate gene expression at the level of

A

mRNA translation and chromatin configuration

18
Q

miRNAs

A

bind to specific mRNA and block translation or signal its degradation
half human genes regulated by miRNAs

19
Q

siRNAs

A

mediate RNAi
formed by different RNA precursors from miRNA but processed by similar enzymes
used in lab to disable genes for study
shown to play role in heterochromatin formation at the centromere in yeast

20
Q

snRNA
snoRNA

A

snRNA: small nuclear RNA
splicing of pre-mRNA

snoRNA: help process and chemically modify rRNA

21
Q

piRNA

A

Piwi-interacting RNA: bind piwi proteins, protect germ line from transposable elements (jumping from one part of genome to another)

22
Q

marking proteins for degradation

A

marking with ubiquitin
ubiquitin is recognized by proteasomes which are large protein complexes that degrade protein

23
Q

stages of embryonic development

A

cell division, cell differentiation and morphogenesis

24
Q

cytoplasmic determinants

A

RNA, protein and other things unevenly distributed in unfertilized egg, influences early development
determination is irreversible, followed by differentiation
results in differential expression of genes

25
Q

Inductive signals

A

signals from embryonic cells target nearby cells and cause transcriptional changes inducing differentiation of specialized cell types

26
Q

pattern formation in embryonic development

A

development of spatial organization of tissues and organs along the major axes
maternal effect genes encode cytoplasmic determinants, or egg-polarity genes developing segmentation in flies

27
Q

bicoid gene example

A

type of maternal effect gene
affects front half of body, no bicoid gene, a fly ends up with 2 back ends

28
Q

morphogens

A

gradient of molecules that determine polarity and position in an embryo in early development, controlled by maternal effect genes

29
Q

homeotic genes

A

control pattern formation in late embryo, larvae and adult stages
mutation causes misplacement of structures

30
Q

proto-oncogenes vs oncogenes

A

cellular genes responsible for normal cell growth and division
mutated proto-oncogenes which are cancer-causing (abnormal stimulation of cell cycle)

31
Q

conversion of proto-oncogene to oncogene can be from:

A

1) translocation closer to promoter
2) amplification of proto-oncogene
3) point mutations of gene or control elements leading to increase in gene expression

32
Q

Ras

A

proto-oncogene, leads to hyperactive Ras which leads to increased cell division (MAPK pathway)
common in human cancers

33
Q

tumor-suppressor proteins

A

1) repair damaged DNA
2) control cell adhesion
3) cell signaling to inhibit cell cycle (ex. in case of damaged DNA)

decreases in these genes can lead to cancer onset

34
Q

p53

A

mutations in p53 tumor suppressor gene are common in human cancers
prevents transcription of faulty DNA

35
Q

a cancerous cell usually contains

A

at least one active oncogene and a few inactive tumor suppressor genes
requires accumulation of cancerous mutations to develop cancer

36
Q

common gene mutation in colorectal cancer

A

mutation of tumor-suppressor gene adenomatous polyposis coli (APC)

37
Q

types of breast cancer
additional mutation found in most types

A

luminal A/B, HER2, basal like
BRCA1/BRCA2 mutation

38
Q

Luminal A and B breast cancer

A

over-expressed estrogen receptors (A more than B) and progesterone receptors
lacks expression of HER2
can be treated with Tamoxifen
A type best prognosis and most common, B less so

39
Q

HER2 breast cancer

A

over expression of HER2, no hormone receptors expressed
can be treated with Herceptin
similar frequency and prognosis to luminal B type

40
Q

Basal-like breast cancer

A

no receptors expressed
aggressive, poorer prognosis, less frequent