d3.2 inheritance Flashcards

1
Q

monohybrid influence

A

only one trait

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2
Q

in the same pair of chromosomes (alleles)

A

diff version of the alleles

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3
Q

2 alleles

A

determine what the characteristic should be

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4
Q

single-nucleotide polymorphism

A

can cause different alleles in the gene pool

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5
Q

single nucleotide polymorphism eg

A

blood type

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6
Q

genotype

A

alleles responsible for the characteristics
eg. BB

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7
Q

phenotype

A

characteristic expressed due to the alleles in the dna and the environment

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8
Q

discrete variations

A

either this or that

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9
Q

discrete variations eg

A

male or female

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10
Q

dominant

A
  • usually the dominant allele codes for a protein that is active and carries out a function
  • always expressed in the offspring
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11
Q

co-dominant

A

pair of alleles are both expressed

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12
Q

homozygous

A

alleles for the characteristics are the same
eg. BB

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13
Q

heterozygous

A

alleles for the characteristic are different
eg. Bb

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14
Q

how to figure out genotype

A

cross with homozygous recessive organism
1:1 = heterozygous dominant
1:3 = 2 heterozygous

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15
Q

recessive

A
  • usually the recessive allele code for a non-functional protein
  • may not be expressed int eh offspring
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16
Q

allele

A

different versions of genes that contain information for the same characteristics
eg. eye colour

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17
Q

chromosome

A

made of dna and protein (histone) and contains genes

18
Q

genes

A

heritable factors that control specific characteristics

19
Q

gene locus

A

specific position of a gene on a chromosome

20
Q

homologous

A

same loci same gene

21
Q

how to say location of gene locus

A

chromosome number
p- short arm
q- long arm
number- bands away from the centromere

22
Q

autosomal recessive disorder

A

not on the chromosome that determines gender

23
Q

autosomal dominant disorder

A

achondroplastic dwarfism

24
Q

sex linked recessive eg

A

haemophilia
- x linked

25
Q

haemophilia

A

cant make clotting factor VIII so cant clot their blood properly

26
Q

pedigree chart

A

circle- females
square- males
no carriers- dominant

27
Q

phenylketonuria PKU

A

mis-sense mutation in the gene that produce styrosine hydrogenate- phenylalanine cant be converted to tyrosine
= results in developmental problems and seizures

28
Q

recessive + autosomal eg

A

phenylketonuria PKU

29
Q

mis-sense nutation

A

base substitution where the change in a single base results in a different amino acid being produced in the amino acid

30
Q

single nucleotide polymorphism

A

variation at a single nucleotide in the genome could lead to different amino acids and multiple alleles in the gene pool
eg. blood group

31
Q

gene pool

A

can look at the frequency of alleles represented in the reproductive population

32
Q

why blood groups are different

A

different antigens on the surface of the red blood cell

33
Q

why blood type needs to match

A

if detected as a foreign by immune system and attacks → group them tgt → form blood clot → die

34
Q

incomplete dominance eg

A

4 o’clock flower

35
Q

intermediate phenotype

A

expressing a mixture of the phenotypes of the parents

36
Q

phenotypic plasticity

A

traits developed can be influenced by the environment through different gene expressions

37
Q

polygenic inheritance

A

trait is affected by more than one gene

38
Q

polygenic inheritance eg

A

skin colour

39
Q

unlinked genes

A

genes that are not on the same chromosome

40
Q

independent assortment

A

alleles of two different genes are passed into gametes without influencing each other (as long as the genes are located on different chromosomes)

41
Q

gene linkage

A

linked genes are pairs or groups or gene which are inherited together, carried on the same chromosome

42
Q

when does independent assortment not occur

A

between linked genes