variation in chromosome structure Flashcards

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1
Q

variations in chromosome structure are important for which of the following?
A. evolution
B. may result in the production of abnormal offspring
C. may alter the phenotype of an organism
D. all of the above

A

all fo the above

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2
Q

the normal sequences of nine genes on a human chromosome is ABCDEFGHI, where the star represent the centromere. Some humans were found to have the aberrant chromosomes. Name type of chromosomal rearrangement using:
ABC
DGFEHI

A

inversion- change in direction of part of the genetic material along a single chromosome

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3
Q

Non-allelic homologous recombination between repetitive sequences can cause genetic diseases in humans. These diseases are caused by ____
A. changing the copy number of important genes
B. deletion of important genes
C. gene silencing
D. position effect
E. A or B

A

changing the copy number of important genes an deletion of important genes

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4
Q

which of the following expressions denotes an organism with a genome 2n+1?

A

trisomic

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5
Q

the failure of chromosomes to separate during cell division is called ___

A

nondisjunction- failure of chromosome to separate

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6
Q
which describes an organism that has 2 complete sets of chromosomes from different species combined within a single species?
A. diploid
B. Aneuploid
C. autptetraploid
D. allotetraploid
E. mosaic
A

allotetraploid- hybrid cell/individual possessing 4 timex the chromosomes in a haploid organism

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7
Q

if 2 non-homologous chromosomes swap a segment of DNA by recombination, what has occurred?

A

a reciprocal translocation- 2 way transfer

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8
Q

which allopolyploid plant of major importance to Washington State is vigorous hexaploid species that combines the genomes of 3 different original species

A

tritium aestiuvm ( bread wheat)

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9
Q

genetic variation

A

refers to the differences in allele and chromosomes either between members of the same species or between different species

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10
Q

karyotype

A

micrograph of metaphase chromosomes from a cell arranged in a standard fashion

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11
Q

deletion in chromosome

A

portion os chromosome is missing, when a chromosome breaks and fragment is lost

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12
Q

duplication in chromosomes (aka non-allelic homologous recombination)

A

portion of the chromosome is repeated

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13
Q

inversion of chromosome

A

change in the direction of part of the genetic material along a single chromosome

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14
Q

translocation

A

segment of one chromosome becomes attached to a non-homologous chromosome

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15
Q

gene family

A

two or more genes that are similar to each other

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16
Q

breakpoint in inversion

A

location of breaks leading to inversion occurs in a vital gene, it will then disrupt gene function

17
Q

position effect in inversion

A

gene is repositioned in a way that alters its expression

18
Q

aneuploidy

A

variation in the number of particular chromosomes within a set

19
Q

euploid

A

variation in the number of complete sets of chromosomes

20
Q

trisomy (Aneuploidy)

A

2n + 1

21
Q

Monosomy (Aneuploidy)

A

2n-1

22
Q

triploid (euploid)

A

3n

23
Q

tetraploid (euploid)

A

4n

24
Q

auto-polyploidy

A

nondisjunction in meiosis or mitosis results in diploid gametes

25
Q

allopolyploidy

A

2 sets, one from each of 2 different species (hybrid cell)

26
Q

polyploidy

A

possessing more than 2 complete sets of chromosomes

27
Q

point mutations

A

change within a gene in which 1 pair in the DNA sequence is altered

28
Q

synapsis

A

pairing of homologous chromosomes prior to their separation into daughter cells

29
Q

simple translocation

A

chromosomal segment is transferred to a non homologous chromosome

30
Q

reciprocal translocation

A

the exchange of segments from 2 nonhomologous chromosomes