Inheritance D3.2 Flashcards

1
Q

How is a zygote formed?

A

male and female gametes fuse, their nuclei join and double the chromosome number

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2
Q

What is inside of the zygote nucleus?

A

contains two chromosomes of each type and is therefore diploid with two alleles of each gene.

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3
Q

What are hybrids?

A

crossed

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4
Q

What is self pollination in plants?

A

grow male and female in the same plant

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5
Q

P-generation

A

the parental generation or the first-true breeding crossed

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6
Q

F1 generation

A

the first generation of offspring produced by crossing two true-breeding parents. they are typically heterozygous

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7
Q

F1 generation

A

crossing individuals from F1. often exhibits 3:1 ratio

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8
Q

Allele

A

alternate version of a gene that differs by one or a few bases and occupies the same locus on a chromosome

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9
Q

Law of segreation

A

only one of the two gene copies present in a diploid organism is distributed to each gamete that it makes during meiosis.

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10
Q

Genotype

A

the genetic makeup of the organism and codes for the phenotype. symbolic representation of a pair of alleles.

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11
Q

Phenotype

A

observable traits

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12
Q

Phenotypic plasticity

A

gene expression changes in order to become adapted to specific environmental conditions. it is reversible as alleles remain unchanged.

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13
Q

Phenyletonuria

A

genetic disease caused by a recessive allele of a gene, mutation of ene on chromosome 12 coding for the enzyme phenylalanine hydrolase. disruptions with neurotransmitters in the brain: mental disorders

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14
Q

Codominance

A

both alleles are expressed independently in the phenotype and are uniquely recognizable.

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15
Q

Roan

A

cows with red and white coats

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16
Q

Incomplete dominance

A

the action of one allele does not completely mask the other

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17
Q

What is codominance and incomplete dominance denoted by?

A

CW CR

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18
Q

Gene pool

A

the genes of all the individuals in a sexually reproducing population

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19
Q

What are some characteristics of the gene pool?

A
  • only one copy of an allele can exist on each chromosome - an individual can only inherit two alleles rather than the full number available in the gene pool.
  • contains many different alleles of a gene due to existence of multiple alleles caused by SNPs.
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20
Q

Single nucleotide polymorphism

A

an alternate version of a gene can be created.
- many different versions of a gene exist, there can be multiple alleles of any gene.
- nucleotide change

21
Q

The existence of more than two phenotypes

A

some genes dont only have two alleles but three, four, five…

22
Q

What is the existence of more than two phenotypes dependent on?

A

dominant/recessive/codominant/etc

23
Q

What gene codes for the production of glycoproteins in ABO blood groups?

24
Q

Which sex chromosome is larger?

A

X, therefore Y contains less genes: some are unique to Y some are shared with X

25
Q

Where is the SRY gene located on and what is it?

A

Y, sex determining region

26
Q

What does the SRY gene do?

A

causes the gonads of a fetus to develop testes of a male. release of the testes determining factor from the embryo. undifferentiated goads turned into testes to release testosterone

27
Q

Sex-linkage

A

inheritance of genes on sex chromosome

28
Q

Characteristics of the sex-linkage inheritance

A
  • typically carried on the X in the non-homologous region
  • different from inheritance on autosomes because X is longer and carries more genes
29
Q

Carrier

A

a person with heterogeneous genotype with a recessive allele of a gene that does not have an effect on their phenotype.

30
Q

Haemophilia

A

recessive and x-linked result in lack of clotting factor being produced in blood plasma. clotting stops bleeding following an injury.

31
Q

Characteristics of Haemophilia

A
  • most common in menn
  • prognosis poor = males did not live long enough to pass allele to female offspring
32
Q

Pedigree charts

A

show patterns of inheritance in a family for a specific trait (phenotype). genotypes can usually be determined.
- tracking of many genetically inherited diseases
- deduction of an allele as recessive/dominant/etc

33
Q

Autosomal recessive

A

both parents no BUT offspring is = recessive
both parents yes = all offspring yes

34
Q

Autosomal dominant

A

both parents yes BUT offspring not = dominant
yes offspring must have at least one affected parent

35
Q

X linked recessive

A

never father to son. more males than females. all males affected recieve from mom.

36
Q

X linked dominant

A

all daughters from fathers affected will have the trait. son will only inherit from mom on her X since Y is inherited from dad. more females.

37
Q

Continuous variation

A

a continuous range of types is possible, with no distinct categories so there are many possible phenotypes. it is influenced by multiple genes if there is a genetic cause. environmental factors may influence trait.

38
Q

Discrete variation

A

separate categories of variation with no intermediates between them so there are few phenotypes. influenced by just one or most a few genes if there is a genetic cause. environmental no effect

39
Q

Polygenic

A

three or more alleles contribute to inheritance. influenced by environment

40
Q

Box and whisker plots

A

show difference in mean and range of a series of data.

41
Q

Independent assortment

A

the part of each parent separate and only one allele passes from each parent to an offspring.

42
Q

Which allele is inherited in independent assortment?

A

dependent on chance due to random orientation of chromosomes in metaphase I. any combination of gametes is possible and eqyually likely.

43
Q

Autosomal gene linkage

A

the genes of an individual can be located on the same chromosome

44
Q

Linkage group

A

all the genes that have their loci on the same chromosome type.
- linked genes may not follow independent assortment and are mostly inherited together.
- when sections of chromosome is exchanged in crossing over, diff alleles may swap positions leading to recombinants.

45
Q

Behavior during meiosis of two alleles

A

depends on their proximity or closeness to each other. the closer together linked genes are positioned, the less likely transferring allele from one chromosome to another.

46
Q

Recombinant

A

a chromosome or DNA with a new combination of alleles due to crossing over in meiosis. the combination of characters is diff from original parents.

47
Q

How can frequency of recombinants be measured

A

by crossing individuals that are het for both genes to individuals that are hoo recessive for both.

48
Q

What does Chi-Squared test determine?

A

difference between an observed and expected frequency distribution is statically correct