lecture 8 Flashcards

1
Q

humans have how many chromosomes

A

46

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2
Q

humans have two copies of each chromosome, therefore they have

A

23

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3
Q

the complex of DNA, histones and non-histone proteins with in the nucleus of a eukaryotic cell. the material of which chromosomes are made

A

chromatin

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4
Q

one of the two copies of a replicated chromosome that is joined at the centromere to the other copy

A

chromatids

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5
Q

two identical chromatids

A

sister chromatids

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6
Q

center of sister chromatids that hold them together, where kinetochore forms

A

centromere

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7
Q

prokaryotes have chromatin?

A

no, they have chromosomes that are “naked” no proteins bonded. Chromosomes live in spaghetti form

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8
Q

three main things chromatin does

A

genome compaction
genome integrity
gene expression regulation

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9
Q

explain genome compaction

A

allows genome to fit into nucleus

  • twice around nucleosome
  • wrapped around itself- 20 nm fibers (might not exist)
  • rope
  • wrapped rope
  • chromsome

can be open, closed and remodeled
-chromatin remodeling enzymes

Histones acetylation (becomes less + charged) loosens its grip on DNA and DNA can be moved around

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10
Q

explain genome integrity

A

protects genome from transposable elements (40% of genome) and DNA damage

when DNA is compacted bad things cant get in and TEs can’t react and cut itself out

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11
Q

explain gene expression regulation

two types of chromosomes

A

heterochromatin

dark are silent. chromosome is binded up and does not allow transcription factors to attach

euchromatin
light is active. chromosome is unbinded and allows transcription factor to attach

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12
Q

histone is made of

A

2 copies of H2A, H2B, H3 and H4

two copies of H3 and H4 bind to form H3-H4 tetramer

one copy of each H2A and H2B form a dimer
(happens twice)

H1 is a linker

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13
Q

explain 3 ways chromatin remodeling enzymes can work

A

sliding
histone exchange
nucleosome eviction

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14
Q

explain 3 ways chromatin remodeling enzymes can work

A

sliding
histone exchange
nucleosome eviction

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15
Q

TEs

A

transposable elements

have matching ends, can cut itself out and then can paste back into genome somewhere else

if DNA is compacted, TEs can not interact with each other

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16
Q

euchromatin

A

low nucleosomal density-
open
active transcription
light part of nucleus

17
Q

heterochromatin

A

high nucleosomal density
closed
non active- silent transcriptionally
dark part of nucleus

18
Q

histones tails

A

unfolded peptides that stick out

can have post translational modifications -(where acetylation occurs)
can activate or deactivate regions

19
Q

chromosomes like to stay in ___

A

discrete territories and with limited intermingling

20
Q

euchromatic regions like to be ___

A

close to the middle of the nucleus

21
Q

heterchromatic regions like to be ___

A

at border of nucleus

22
Q

explain DNA replication at the end. explain telomeres

A

DNA polymerase can only add to the 3’ has to go 5’ to 3’

RNA primers are added first and DNA polymerases extend the new strand after the primer

RNA primers are removed afterwards. DNA polymerase will fill in gaps where the primer was

at the end of the chromosome, primer is not added

therefore, at the end of DNA replication, 50-100 nucleotides are lost (BAD THING) too short=cell death

23
Q

telomerase

A

telomerase has an associated RNA that complements the 3’ overhang at the end of he chromosome

the RNA template is used to synthesize the complementary strand

telomerase is shifted and process is repeated

primase and DNA polymerase synthesize the complementary strand

active typically only in germ cells and stem cells

improper activation is contributor as how cancer replicates

24
Q

errors in telomerase

A

cancer- cells are replicated without shortening- can live forever!

25
Q

down syndrome

A

trisomy 21- XXY

two many chromosome

26
Q

deletion of one of two chromosomes

A

monosomy

27
Q

chromosomal duplication

A

polyploidy

28
Q

part of one arm of a chromosome is transferred to an arm or different chromsome

A

translocation

29
Q

example of translocation error

A

blood cancers

t(15;17)(q24;a21)- acute promyelocytic leukemia (APL)

30
Q

polyploidy and monosomy cause disease by generating

A

improper levels of gene expression

31
Q

translocations cause diseased by creating

A

improper proteins

32
Q

*** why does acetylation of histone N terminal tails correlate with high transcriptional activity?

A

acetylation neutralized the positive charge of the histone, decreasing the histones ionic interaction with the negative charge of DNA. This allows DNA to be exposed (TATA box, promoters) thus allowing transcription to occur

acetylation makes histone less +, loosens grip on -DNA, DNA can move/unbind and can be acted upon by transcription factors