The Central Dogma Flashcards

1
Q

What is true of cells and their expression of genes?

A

Often, cells are always expressing genes, but at different amounts and rates, due to a difference in the ability of specific transcription factors.

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2
Q

What are 5 general places to regulate gene expression?

A

Chromatin remodeling, transcription factor regulation, mRNA splicing/maturation, destruction of mRNAs, or protein level phosphorylation

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3
Q

Nucleosome

A

Histone octamer surrounded by DNA

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4
Q

Inactive genes [methyl/acetyl]

A

Methylated DNA in promoter, and methylated, deacetylated histones

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5
Q

Active genes

A

acetylated, non-methylated histones

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6
Q

What do acetyl groups do to histones?

A

It spreads them apart, unwinding the DNA

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7
Q

Promoter

A

sequence that starts the sequence of an active gene

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8
Q

What are CpG islands?

A

They are places where a transcription factor binds and activates a promoter to transcribe the active gene

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9
Q

Where is DNA methylation high?

A

In primordial germ cells, right before fertilization, and at the embryo stage.

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10
Q

General transcription factors

A

bind to gene promoters and organize the transcriptional machinery

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11
Q

Regulatory transcription factors

A

bind to enhancers to make transcription more or less efficient

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12
Q

Where is the TATA box located?

A

In the promoter sequence.

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13
Q

What must be true before RNA polymerase can bind to the gene?

A

Several General transcription factors must be present

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14
Q

How to regulatory transcription factors interact with enhancers?

A

They can create a 3d complex such as the mediator complex which more easily allow RNA polymerase to bind.

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15
Q

Where in relation are enhancers located to the active gene?

A

Usually far away

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16
Q

What are two properties of regulatory transcription factor binding that promotes differentiation and variation?

A

Combinations of transcription factors, and cascades can induce variability

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17
Q

How do transcription factors ensure differential gene expression?

A

Specific tissues have specific transcription factors that activate tissue specific enhancer sequences

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18
Q

MyoD1 [explanation, sufficiency/necessity]

A

Can induce differentiation into muscle. is sufficient, but not necessary, as this works with myf5 as well

19
Q

What is the technical name of something that promotes differentiation into muscle?

A

myogenic factors

20
Q

Pax6

A

induces differentiation into eye tissue

21
Q

How can you study transcriptional regulation without changing the gene’s natural function?

A

Fuse the regulatory DNA associated with a gene to a “reporter” e.g GFP

22
Q

Splicing

A

taking specific exons out of the nRNA , can make many combinations.

23
Q

5’ cap

A

translatability

24
Q

3’-UTR

A

mRNA localization, regulation of translation

25
Q

poly A tail

A

mRNA stability, translation

26
Q

Polyadenylation element

A

AAUAAA catalyze addition of As to the tail.

27
Q

Where do RNAs usually end up in the Oocyte?

A

In the vegetable pole

28
Q

What is nanos mRNA

A

mRNA that is being currently translated

29
Q

What section of mRNAs attach to microtuble motors?

A

The 3’-UTR region

30
Q

Which direction do kinesins travel?

A

Toward the posterior end of the cell [Positive]

31
Q

Which direction do dyneins move?

A

Toward the anterior end of the cell [Negative]

32
Q

What do bicoid mRNAs attach to? [which motor]

A

Dyneins

33
Q

What do oskar mRNAs attach to? [which motor]

A

Kinesins

34
Q

What are two ways that mRNA translatability can be affected?

A

The Maskin/CPEB/4E complex, and the Bicoid/Caudal complex.

35
Q

How is the Maskin/CPEB/4E complex changed after fertilization?

A

CPEB is phosphorylated, poly(A)polymerase is recruited, building As which can bind poly(A) binding protein(PABP), which can finally initiate translational cofactors at the 5’ end.

36
Q

The maternal to zygotic transition varies in time between species [true/false]

A

true

37
Q

What is the name of small RNAs that regulate mRNAs?

A

micro RNAs, [miRNAs]

38
Q

First stage of a microRNA

A

pri-miRNA (primary micro RNA)

39
Q

Pri-miRNA is processed to ____ by ____ in the second step

A

Pri-miRNA is processed to pre-miRNA by Drosha

40
Q

Pre-miRNA is processed by ____ into short double stranded RNA duplexes.

A

Dicer

41
Q

RISC choices

A

if the mRNAs match, then the mRNA is destroyed. If the match is inexact, translation is blocked.

42
Q

Degradation of proteins is marked by ____ to be sent to the ____ for destruction

A

Degradation of proteins is marked by ubiquitins to be sent to the proteasome for destruction

43
Q

What famous signaling pathway that we have been studying uses proteasome?

A

Wnt B catenin signaling. In the absence of Wnt signaling, GSK-3, and APC add ubiquitins to Beta catenin, destroying it.