Chapter 10 part 2 Flashcards

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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

A

both

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 _______

A

2n-2

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
Q

What are the 5 types of histone proteins?

A

1) H1
2) H2A
3) H2B
4) H3
5) H4

26
Q

_______ are fundamental units of histone protein organization with two molecules of each histone (not including H1)

A

nucleosome core particles
- DNA around nucleosome is first level DNA condensation

27
Q

How are nucleosomes assembled?

A

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
Q

The variable length between nucleosomes is called _______

A

linker DNA

29
Q

the 30-nm fiber forms when the 10 nm fiber coils into a _______ with 6-8 nucleosomes per turn

A

solenoid
- second level of DNA condensation

30
Q

What Histone stabilizes solenoids?

A

H1

31
Q

Chromosome shape depends on the chromosome _______, composed of filamentous, non-histone proteins

A

scaffold

32
Q

Chromatin loops are anchored to the chromosome scaffold by nonhistone proteins at sites called _______

A

MARs (matrix attachment regions)

33
Q

_______ syndrome is found in partial deletion of heterozygotes for segment of chromosome 7 that contain duplicate copies of PMS

A

Williams-beuren