Exam 1: Lecture 11 Flashcards

1
Q

inversion depends on the involvement of the _ in the inversion

A

centromere

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2
Q

paracentric inversion

A

does not include centromere (confined to one arm of a chromosome)

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3
Q

pericentric inversion

A

change in position of centromere; occur on both arms of a chromosome and spans the centromere

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4
Q

an inversion in mitosis, if balanced usually no problems in mitosis, t/f?

A

true

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5
Q

an inversion in meiosis: homozygous individuals

A

no problems arise during meiosis

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6
Q

an inversion in meiosis: heterozygous individuals

A

para- or peri- centric inversion often have nonfcnal gametes due to loss of large amounts of genetic material during meiosis

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7
Q

an indiv heterozygous for a para/pericentric inversion, what occurs?

A

the chromosomes form an inversion loop during pairing in prophase I

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8
Q

in a heterozygous indiv, a single crossover within a paracentric inversion leads to

A

abnormal gametes

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9
Q

crossing over within para inversion leads to (het)

A

unusual structure, one of the 4 chromatids now has 2 centromeres and 1 lacks a centromere

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10
Q

what happens in anaphase I of meiosis during paracentric inversions (het)

A

centromeres separate, stretching the dicentric chromatid (from crossing over) which breaks. The chromosome lacking a centromere is lost

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11
Q

what happens in anaphase II of meiosis during paracentric inversions (het)

A

2 gametes contain non-recombinant chromosomes: one WT (normal) and one with inversion. The other 2 contain recombinant chromosomes that are missing some genes; these gametes will not produce viable offspring

resulting recombinant gametes are nonviable bc they are missing some genes

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12
Q

what happens in crossing over of a peri inversion (het)

A

2 of the resulting chromatids have too many copies of some genes and no copies of others

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13
Q

what happens in anaphase I of peri inversion (het)

A

chromosomes separate in anaphase I

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14
Q

what happens in anaphase II of peri inversion (het)

A

sister chromatids separate in anaphase II forming 4 gametes; recombinant gametes are nonviable bc genes are either missing or present in too many copies

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15
Q

translocations are caused by:

A

rearrangement of segments between nonhomologous chromosomes

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16
Q

a translocation can be balanced if:

A

in an even exchange of material with no genetic information duplicated or lost, and usually fully functioning

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17
Q

a translocation can be unbalanced if:

A

the exchange of genetic material is unequal resulting in extra or missing genes

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18
Q

reciprocal translocation

A

an exchange of material btwn nonhomologous chromosomes

19
Q

nonreciprocal translocation

A

transfer of genes from one chromosome to another nonhomologous chromosome

20
Q

robertsonian translocation

A

recombining with acrocentric chromosomes that allow the short arms to be lost and the long arms creating metacentric chromosome

21
Q

translocation in meiosis infertility:

A

gametes resulting from adjacent-I and adjacent-2 segregation are nonviable bc of the loss or gain of large amts of DNA (missing or 2 copies)

22
Q

it is thought that humans and chimpanzees are more closely related than chimpanzees and gorillas or orangutans.

how can you explain that chimpanzees, gorillas and orangutans all have 2 chromosomes that contain the genes on chromosome 2 of humans?

A

the human chromosome combined and formed one singular stable chromosome that may be similar to the 2 chromosomes in chimpanzees, gorillas, and orangutans, but the genes on human chromosome 2 are not used the exact same way/amount they are used in the 2 chromosomes of primates

23
Q

chromosome 4 differs in humans and chimpanzees due to a

A

pericentric inversion; genes around centromeres is rearranged differently

24
Q

cen

A

centromere

25
del
deletion
26
der
derivative chromosome (translocation)
27
fra
fragile site
28
dic
dicentric chromosome
29
dup
duplication
30
what are the causes of aneuploidy
- deletion of centromere during mitosis and meiosis - robertsonian translocation - nondisjunction during mitosis/meiosis
31
types of aneuploidy: 2n - 2
nullisomy: loss of both members of a homologous pair of chromosomes
32
types of aneuploidy: 2n - 1
monosomy: loss of a single chromosome
33
types of aneuploidy: 2n + 1
trisomy: gain of a single chromosome
34
types of aneuploidy: 2n + 2
tetrasomy: gain of 2 homologous chromosomes
35
effects of aneuploidy in plants
trisomies product different seed cases for a different plant (mutants could actually be trisomics)
36
effects of aneuploidy in humans
sex-chromosome aneuploids: - turner syndrome XO - klinefelter syndrome XXY
37
autosomal trisomy in humans
trisomy 21 down syndrome
38
what is primary down syndrome
nondisjunction in egg formation
39
what is familial down syndrome
robertsonian translocation
40
translocation carriers are at an increased risk for what
producing children with down syndrome
41
autopolyploidy
from single species
42
allopolyploidy
from 2 or more species
43
the significance of polyploidy
increase in cell size, larger plant attributes, evolution (give rise to new species)
44
autopolyploidy do not segregate in anaphase and result in
unreduced cell (common in cancer) also happens in meiosis