quiz 2 deck Flashcards

1
Q

Explain the difference between biological sex and gender

A

sex of an individual is determined based on its phenotype

gender is not the same as sex
-one’s gender does not need to consider with ones’s biological sex

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2
Q

Describe the major sex-chromosome sex determining systems, including XX-XO, XX-XY, and
ZZ-ZW systems

A

FEMALE MALE
xx xo
xx xy
zw zz

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3
Q

Explain how sex is determined in the genic sex-determining system

A

Sex determination is determined by individual genes
In chromosomal sex determination the sex chromosomes look different in males and females

in genetic sex determination: there are no obvious differences in the chromosomes of males and females (cant tell M or F)

sex is determined by genes, but the chromosomes of males and females are indistinguishable
In genic the chromosomes also look different in male and females

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4
Q

Describe environmental sex determination

A

sexual phenotype affected by temeprature during embryonic development
Sex chromosomes determine sex, but environment overrides this
sequential hermaphroditism: each individual can be both male and female, but not at the same time

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5
Q

Explain how sex in humans is determined

A

sex is inherited like other genetically determined characteristics , presence of sry gene

xx and xy

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6
Q

Describe several sex chromosome anomalies in humans.

A

Poly x females (mostly fertile)
xyy males (generally normal physical characteristics
Klinefelter syndrome: xxy, xxxy, xxxxy,xxyy, MALE. at least 1 y chromosome and multiple x, sterile
turner syndrome xo (female, single x chromosome, sterile)

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7
Q

Explain the origin of androgen insensitivity syndrome

A

Female in apperance with xy chromsomes caused by defective androgen receptor
cells do no respond to testerone

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8
Q

List the characteristics of Y-linked traits

A

Inherited from the father and is displayed in all male offspring, not female

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9
Q

predict the number of Barr bodies present in cells with different complements of sex
chromosomes

A

Random inactivation of one x chromosome in cells of females (barr bodies)
xxy -1
xxyy-1
xxxy-2
xxxxy-3
xxx-2
xxxx-3
xxxxx-4

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10
Q

Describe the molecular mechanism by which random inactivation of X chromosomes occurs

A

all somatic cells that descend from inactive cell remain inactive (why they can be passed on)
it is a type of epigenetics?

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11
Q

Explain the differences between complete, incomplete, and codominance.

A

Complete: phenotype of the herteozygote is the same as the phenotype of one of the homozygotes

Incomplete:phenotype of the heterozygote is the intermediate between the phenotypes of the two homozygotes

codominance: phenotype of the heterozygote includes the phenotypes of both homozygotes

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12
Q

Predict the proportions of offspring produced when penetrance is incomplete

A

Incomplete penetrance: the genotype does not alwasy produce the expected phenotype

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13
Q

Describe the difference between incomplete penetrance and variable expressivity

A

Expressivity: the degree to which a trait is expressed

Incomplete penetrance: the genotype does not always produce the expected phenotype

Polydactly example:
incomplete penatrance: polydactly trait caused by a dominant allele children has polydactly but parents don’t although he should, gene for polydactly is not fully penetrant

Expressivity: polydactly exhibit variable expressivity; some ppl have extra toes while some have extra skin

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14
Q

Explain how genic interaction differs from dominance

A

Dominance is an interaction between alleles at a single locus, gene interaction happens at different loci

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15
Q

Explain why one might want to carry out a complementation test.

A

In instances when two parent organisms each carry two mutant genes in a homozygous recessive state, causing the recessive trait to be expressed, the complementation test can determine whether the recessive trait will be expressed in the next generation.

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16
Q

Recognize the characteristics of cytoplasmically inherited traits (sperm blows shit out of proportion)

A

mitochondira
typically all its cytoplasmic organelles and thus cytoplasmic genes , come from only on gamete
egg usually contribute cytoplasmic organelles and sperm usually contributes only nuclear genes

17
Q

Describe the differences between sex-influenced characteristics, sex-limited characteristics,
cytoplasmically inherited traits, genetic maternal effect, genomic imprinting, and anticipation

A

Sex-influenced characteristics: These are traits that are influenced by sex hormones, but the expression of the trait is not limited to one sex. For example, baldness is influenced by the male hormone testosterone, but it can also occur in females.

Sex-limited characteristics: These are traits that are expressed in only one sex. For example, the ability to lactate is limited to females.

Cytoplasmically inherited traits: These are traits that are inherited through the cytoplasm of the cell, rather than through the nuclear DNA. Mitochondrial DNA is an example of cytoplasmically inherited genetic material.

Genetic maternal effect: This is a type of inheritance where the phenotype of the offspring is determined by the genotype of the mother. In this case, the mother’s genes determine the phenotype of the offspring, regardless of the offspring’s own genotype.

Genomic imprinting: This is a phenomenon where the expression of a gene depends on whether it was inherited from the mother or the father. In genomic imprinting, certain genes are silenced or expressed depending on which parent they were inherited from.

Anticipation: This is a phenomenon where the severity or age of onset of a genetic disorder increases in successive generations. For example, in Huntington’s disease, the age of onset of symptoms tends to decrease in each generation, resulting in an earlier onset of symptoms in the offspring.

Overall, these genetic concepts illustrate the complex nature of inheritance and how different factors can influence the expression of traits and disorders.

18
Q

Explain how environmental factors affect the expression of traits

A

temperature and ph sensitive allele

19
Q

Explain the difference between polygeny and pleiotropy

A

Polygeny refers to the situation where a trait or disorder is determined by the combined effect of multiple genes. In contrast, pleiotropy refers to the situation where a single gene affects multiple traits or functions. Polygeny results in a continuous range of variation in the trait, while pleiotropy often results in a complex pattern of inheritance, as the same gene can affect multiple traits in different Pleiotropy often results in a complex pattern of inheritance, as the same gene can affect multiple traits in different ways.

20
Q

Explain what a polygenic characteristic is.

A

a part of a continous characteristic: characteristics that display a large number of possible phenotypes that are not easily distinguished. characteristics encoded by genes at many loci.
Polygeny refers to the situation where a trait or disorder is determined by the combined effect of multiple genes. In other words, the phenotype of the trait is influenced by the interaction of several genes. Polygeny often results in a continuous range of variation in the trait, rather than distinct categories.