D3.2 Inheritance Flashcards

1
Q

describe Gregor Mendel’s experiment and his findings

A
  1. placed homozygous dominant male pollen into recessive female ovaries of pea plants
  2. F1 generation 100% heterozygous
  3. F2 generation 1:2:1 (homozygous dominant:heterozygous:recessive), 3:1 (dominant:recessive)
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2
Q

when did Mendel conduct his pea experiment, and what did he first call genes?

A

1865; factors

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3
Q

allele

A

version of gene; codes same trait but different variations

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4
Q

heterozygote

A

organism with 1 dominant, 1 recessive allele of a gene

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5
Q

homozygote

A

organism with either 2 dominant or 2 recessive alleles of a gene

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6
Q

monohybrid cross

A

cross between two parents focusing on just 1 trait (eg Tt×TT, ff×FF, Gg×Gg, etc)

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7
Q

draw two Punnett grids representing Mendel’s experiment findings

A
  1. TT×tt = Tt, Tt, Tt, Tt
  2. Tt×Tt = TT, Tt, Tt, tt
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8
Q

what is a carrier of a gene?

A

heterozygous organism having recessive allele that doesn’t affect its phenotype

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9
Q

examples of phenotypical characteristics exclusively due to genetics

A

ABO blood, Huntington’s, colour blindness, cystic fibrosis

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10
Q

examples of phenotypical characteristics exclusively due to envrionment

A

learning math and songs, scars, large muscles

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11
Q

examples of phenotypical characteristics due to both genetics and environment

A

height, cancer

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12
Q

codominant alleles

A

when heterozygote has two alleles that are dominant and both phenotypes are expressed (eg having both IA and IB alleles results in AB blood type)

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13
Q

incomplete dominance

A

when heterozygote has two alleles that are dominant and neither phenotype is expressed, only a mix (eg mixing pure-bred white and red four o’clock flowers results in pink flowers)

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14
Q

phenotypic plasticity

A

ability to express phenotype differently based on environment (adaptation)

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15
Q

phenological events

A

phenological changes based on changes in environment during cyclical events (like seasonal food availability)

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16
Q

how does freshwater snail physa virgata employ phenoplastic plasticity?

A

shell normally conical and elongated, different genes expressed to become rounded when predator around so harder to crush

17
Q

phenylketonuria

A

autosomal disease from PAH gene mutation, resulting in decreased production of phenylalanine hydroxylase, which converts toxic phenylalanine from proteins to tyrosine

18
Q

examples of autosomal recessive diseases

A

albinism, cystic fibrosis, sickle cell disease, Tay Sachs, thalassemia

19
Q

how do humans taste bitterness?

A
  1. if one has TAS2R38 gene that codes for taste receptor 2 member 38, phenylthiocarbamide can attach to receptor, allowing taste bitterness
  2. single-nucleotide polymorphisms make alleles of TAS2R38 gene, which don’t code for receptor
20
Q

how many alleles, genotypes, and phenotypes contribute to ABO blood type?

A

3 alleles, 6 genotypes, 4 phenotypes

21
Q

what are the two types of chromosomes?

A

22 autosomes, 1 pair allosomes (sex chromosomes)

22
Q

differences between X and Y chromosomes

A
  1. X codes for oestradiol and progesterone production, Y for testosterone
  2. Y 70 genes vs X 800, most genes on X no allele on Y to pair with
23
Q

what determines sex in humans?

A

XX = female, XY = male; sperm determine gender (50% sperm have Y, 50% X)

24
Q

sex-linked trait

A

genetic trait with gene locus on X (rarely Y) chromosome; often affects males more

25
Q

haemophilia

A

sex-linked recessive trait caused by allele on X chromosome causing trouble blood clotting

26
Q

what kind of trait is huntington’s

A

autosomal dominant trait

27
Q

draw a pedigree chart of the P and F1 generations of a female without huntington’s and a male heterozygous for it

A

hh × Hh = hh, Hh, Hh, hh

28
Q

what effect does incest have on genetic diseases?

A

increases frequency of rare diseases (eg families with Huntington’s are 50% affected while general population only 0.01%)

29
Q

polygenic inheritance

A

when multiple genes influence expression of 1 trait, increasing possible genotypes and allowing continuous variation

30
Q

continuous variation

A

when continuous array of phenotypes possible because of polygenic inheritence (eg intensity of skin colour controlled by at least 4 genes controlling melanin production)

31
Q

discrete variation

A

when only 1 gene responsible for trait, allowing discrete phenotype options; can be shown on bar graph

32
Q

dihybrid cross

A

cross between two parents focusing on 2 traits (eg RrYy×RrYy, RRYY×rryy, etc)

33
Q

mendelian ratios for dihybrid cross results

A
  • 9:3:3:1 for 2 parents heterozygous for both traits
  • 1:1:1:1 for 1 parent heterozygous for both traits, 1 parent recessive for both traits (test cross)
34
Q

what were mendel’s two laws?

A
  • law of segregation: each gamete only receives 1/2 copies from each parent (meiosis)
  • law of independent assortment: each chromosome is inherited independent of each other, unless on same chromosome/too close to be shuffled in crossing over (recombination rate under 50%)
35
Q

linked genes

A

on same chromosome/close together, usually passed down together; changes predicted ratios of dihybrid crosses

36
Q

what is a group of linked genes called?

A

linkage group

37
Q

draw possible offspring genotypes for a fruit fly heterozygous for brown body and normal wings, and another homozygous for black body and vestigial wings (with crossing over)

A

BbVv×bbvv = BbvV×bbvv = Bbvv and bbVv