Chapter 10 part 2 Flashcards

1
Q

When a chromosome breaks, both DNA strands are severed at a location called a _______

A

chromosome break point

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2
Q

Detachment of all or part of one chromosome arm can lead to a _______; the broken fragment contains a telomere and some genetic material

A

terminal deletion

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3
Q

If any broken chromosome fragment is _______, it will likely be lost during cell division as it can’t attach to the spindle apparatus

A

acentric

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4
Q

_______ is an example of chromosome deletion and is caused by the loss of 5p15.2-5p15.3

A

cri-du-chat syndrome

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5
Q

_______ is the loss of an internal portion of a chromosome and results from 2 chromosome breaks

A

interstitial deletion

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6
Q

_______ is a series of conditions caused by interstitial deletion of multiple genes on chromosome 11

A

WAGR syndrome

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7
Q

an organism with one normal and one duplication homolog is a _______

A

partial duplication heterozygote

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8
Q

Unequal crossover does not occur often and most commonly occurs when repetitive regions such as _______ and _______ of homologs misalign

A

PMSA
PMSB

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9
Q

Large deletions and duplications are identified by a _______, which is the part of one homolog missing on the pairing partner

A

unpaired loop

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10
Q

Micro-deletions and micro-duplications can be identified by _______

A

FISH

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11
Q

Sometimes chromosome breakage leads to attachment of the wrong broken ends leading to _______ on the same chromosome or _______ to a nonhomologous chromosome

A

chromosome inversion
chromosome translocation

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12
Q

_______ when the centromere is outside of the inverted region

A

paracentric inversion

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13
Q

_______ when the centromere is within the inverted region

A

pericentric inversion

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14
Q

_______ have one normal and one inverted homolog

A

inversion heterozygotes

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15
Q

Crossing over within a paracentric inversion results in _______ and ______

A

dicentric chromosome
acentric chromosome

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16
Q

Crossing over within a pericentric inversion results in both duplicated and deleted regions in _______ of the recombinant products

17
Q

Both paracentric and pericentric inversions result in _______ and _______

A

2 viable chromosomes
2 nonvialble chromosomes

18
Q

What are the 3 different types of translocations?

A

1) unbalanced (one way transfer)
2) reciprocal balanced (two way transfer)
3) Robertsonian (fusion)

19
Q

In reciprocal balanced translocations, _______ structure is formed at metaphase I of meiosis.

A

cross-like

20
Q

Translocation heterozygotes are _______ because only half of alternate segregation leads to normal gametes

A

semi-sterile

21
Q

If 2 pairs of chromosomes fuse by Robertsonian translocation, the number of chromosomes drops _______

22
Q

One type of robertsonian translocation between chromosome 21 and 14 is reponsible for _______

A

familial down syndrome

23
Q

The DNA and associated proteins of a chromosome are called _______

A

chromatin
1/2 DNA and 1/2 protein

24
Q

_______ are small basic proteins that tightly bind DNA

A

histone proteins

25
What are the 5 types of histone proteins?
1) H1 2) H2A 3) H2B 4) H3 5) H4
26
_______ are fundamental units of histone protein organization with two molecules of each histone (not including H1)
nucleosome core particles - DNA around nucleosome is first level DNA condensation
27
How are nucleosomes assembled?
1) H2A and H2B form dimers 2) H3 and H4 form dimers 3) H3 and H4 dimers form tetramer 4) H2A and H2B associate with H3H4 tetramer to form octamer
28
The variable length between nucleosomes is called _______
linker DNA
29
the 30-nm fiber forms when the 10 nm fiber coils into a _______ with 6-8 nucleosomes per turn
solenoid - second level of DNA condensation
30
What Histone stabilizes solenoids?
H1
31
Chromosome shape depends on the chromosome _______, composed of filamentous, non-histone proteins
scaffold
32
Chromatin loops are anchored to the chromosome scaffold by nonhistone proteins at sites called _______
MARs (matrix attachment regions)
33
_______ syndrome is found in partial deletion of heterozygotes for segment of chromosome 7 that contain duplicate copies of PMS
Williams-beuren