Modern Understanding of Inheritance Flashcards

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1
Q

Aneuploid

A

individual with an error in chromosome number; includes chromosome segment deletions and duplications

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2
Q

Autosome

A

any of the non-sex chromosomes

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3
Q

Centimorgan (cM)

A

(also, map unit) relative distance that corresponds to a 0,01 recombination frequency

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4
Q

Chromosomal Theory of Inheritance

A

theory proposing that chromosomes are the genes’ vehicles and that their behavior during meiosis is the physical basis of the inheritance patterns that Mendel observed

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5
Q

Chromosome inversion

A

detachment, 180° rotation, and chromosome arm reinsertion

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6
Q

Euploid

A

individual with the appropriate number of chromosomes for their species

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7
Q

Homologous recombination

A

process by which homologous chromosomes undergo reciprocal physical exchanges at their arms, also crossing over

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8
Q

Karyogram

A

a karyotype’s photographic image

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9
Q

Karyotype

A

an individual’s chromosome number and appearance; includes the size, banding patterns, and centromere position

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10
Q

Monosomy

A

otherwise diploid genotype in which one chromosome is missing

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11
Q

Nondisjunction

A

failure of synapsed homologs to completely separate and migrate to separate poles during the meiosis’ first cell division

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12
Q

Nonparental (recombinant) type

A

progeny resulting from homologous recombination that exhibits a different allele combination compared with its parents

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13
Q

Paracentric

A

inversion that occurs outside the centromere

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14
Q

Parental Type

A

progeny that exhibits the same allelic combination as its parents

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15
Q

Pericentric

A

inversion that involves the centromere

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16
Q

Polyploid

A

individual with an incorrect number of chromosome sets

17
Q

Recombination Frequency

A

average number of crossovers between two alleles; observed as the number of nonparental types in a progeny’s population

18
Q

Translocation

A

process by which one chromosome segment dissociates and reattaches to a different, nonhomologous chromosome

19
Q

Trisomy

A

otherwise diploid genotype in which one entire chromosome duplicates

20
Q

X inactivation

A

condensing X chromosomes into Barr bodies during embryonic development in females to compensate for the double genetic dose