lecture 25 - inheritance Flashcards

1
Q

inheritance

A

transfer of hereditary traits from one generation to the next

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2
Q

alleles

A

alternative forms of a gene that codes for the same trait and are on the same location on homologous chromosomes

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3
Q

mutation

A

permanent change in an allele that leads to a different version of the same trait

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4
Q

genotype

A

genetic makeup

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5
Q

phenotype

A

phydical expression of a gene

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6
Q

punnett square

A

inheritance of dominant and recessive alleles for normal traits

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7
Q

punnett square example

A

parent 1 = Bb
parent 2 = Bb

B = brown, dominant
b = blue, recessive

outcomes:
BB - brown
Bb - brown
Bb - brown
bb - blue

number of genotypes = 3
number of phenotypes = 2

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8
Q

homozygous

A

two of the same alleles
eg. BB, or bb

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9
Q

heterozygous

A

two different alleles
eg. Bb

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10
Q

punnitt square examples of:

heterozygous dominant trait
homozygous dominant trait
homozygous recessive trait

A

hetero dom - Bb (50%)
homo dom - BB (25%)
homo recessive - bb (25%)

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11
Q

heterozygous alleles can show co dominance, waht does this result in

A

a shared phenotype

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12
Q

dominant allele

A

fully expressed
masks recessive
controls phenotype

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13
Q

recessive allele

A

fully masked by dominant
controls recessive trait

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14
Q

abnormaliteis from cells division (2)

A

nondisjuction
translocation

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15
Q

nondisjunction

A

abnormal number of chromosomes

also called aneuploidy

can be monosomy or trisomy

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16
Q

translocation

A

interchanging of chromosome portions between non homologous chromosomes

17
Q

genetic imprinting

A

mutated gene or and abnormal trait particularily inhertied form teh mother OR father

18
Q

nondisjuction in meiosis 1 results in

A

4 cells:

2 are trisomy
2 and monosomy

19
Q

nondisjunction in meiosis 2

A

4 cells
1 trisomy
1 monosomy
2 normal

20
Q

X and Y protein coding genes numbers

A

X - 1100. Y 60

X is much larger than Y

21
Q

X chromosome inactivation. what is it and function

A

transcriptional silencing of one X in females

  • equalizes gene dosage
  • makes sure there is one functional X in each body cell
  • occurs early in development in all cells except in oocytes

other X becomes a barr body