The Chromosomal Basis of Inherit Flashcards

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1
Q

How do scientists tag the location of isolated chromosomes?

A

Fluorescence in situ hybridization (FISH)

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2
Q

An organisms life cycle

A

The sequence of stages leading from the adults of one generation to the adults of the next

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3
Q

Why do our chromosomes duplicate?

A

Sorts new sets of chromosomes into the resulting pair of daughter cells, for reproduction of single-felled organisms, for growth of multicellular organisms from a fertilized egg into an adult, to repair and replace cells, and for sperm/egg production

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4
Q

How many divisions are in Meiosis?

A

Two sequential divisions

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5
Q

What are the three mechanisms that contribute to genetic variation?

A

Random fertilization (eg. many sperm competing to fertilize egg), independent assortment of chromosomes, and crossing over

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6
Q

Independent assortment

A

Homologous pairs of chromosomes orient randomly at metaphase 1 of meiosis. Each pair of chromosomes sorts maternal and paternal homologs into daughter cells independently of the other pairs

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7
Q

What does 2^n stand for?

A

The number of combinations possible when chromosomes assort independently into gametes (n stands for the haploid number)

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8
Q

Who discovered the first evidence of chromosomal basis for inheritance?

A

Thomas Hunt Morgan in his fruit fly study - noted wild type and mutant traits - reasoned that the white-eyed mutant allele must be located on the X chromosome due to how it was inherited by only male flies in the second generation

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9
Q

Why use flies?

A

They produce many offspring, a generation can be bred every two weeks and they have only four pairs of chromosomes

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10
Q

Sex chromosomes

A

Designated X and Y, determines an individuals sex

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11
Q

What are the four other main types of sex determination

A

The X-0 system: only have one toe if sex chromosome
The Z-W system: females produce eggs that are either Z or W with males gametes being Z (reversed relative to humans)
The haplo-diploid system: no sex chromosomes, instead, females develop from fertilized eggs while males develop from unfertilized eggs
Environmental temperature: temperature determines the sex of the embryo - males develop in colder temperatures while females develop in warmer temperatures

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12
Q

Sex-linked genes

A

Located on either of the sex chromosomes - the X chromosome Carrie’s many genes unrelated to sex

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13
Q

Is colorblindness an X-linked recessive trait?

A

True - all daughters will receive a color blindness allele form their colorblind father making them carriers, sons have a 50% chance of receiving the colorblind allele form their mother (50% chance of being colorblind), and only a daughter born to parents who both carry the color blindness allele could be colorblind

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14
Q

Hemophilia

A

The Royal Disease - characterized by excessive bleeding because hemophiliacs lack one or more of the proteins required for blood clotting

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15
Q

What does the Y chromosome provide clues about?

A

Human male evolution - Y chromosomes are passed intact from father to son

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16
Q

Do females make twice as much as males of the products encoded in the X chromosome?

A

No - one of the X chromosomes is inactivated

17
Q

Germline tissue

A

Produces gametes - expresses both X chromosomes

18
Q

Somatic tissue

A

Found in females, looks like a mosaic, some express maternal X chromosome and others express the paternal X chromosome

19
Q

When one of the two X chromosomes in each cell is randomly inactivated during embryonic development is condenses into what?

A

A Barr body

20
Q

What triggers the inactivation?

A

X-inactive specific transcription (XIST) - XIST mRNA covers the chromosome, chromosomal DNA then has methyl groups attached to it to inactivate it

21
Q

Linked genes

A

Located close together in the same chromosome, tend to be inherited together, and do not follow Mendel’s law or independent assortment

22
Q

What produces new combinations of alleles?

A

Crossing over between homologous chromosomes produces new combinations of alleles in gametes

23
Q

Recombination frequency

A

The percentage of recombinant offspring

24
Q

Map units

A

Distance between genes as equivalent to a 1% recombination frequency

25
Q

Nondisjunction

A

The failure of chromosomes or chromatids to separate normally during meiosis - happens during meiosis 1 (if both members of a homologous pair go to one pole) or during meiosis 2 (if both sister chromatids go to one pole)

26
Q

Karyotype

A

An ordered display of magnifies images of an individuals chromosomes arranged in pairs

27
Q

What does an extra copy of chromosome 21 cause?

A

Trisomy 21 also known as Down syndrome

28
Q

Genomic imprinting

A

Involves the silencing of certain genes depending on which parent passes them on - most imprinted genes are critical for embryonic development

29
Q

How are organelle genes inherited?

A

Through mitochondria, chloroplasts, and other plant plastids that carry small circular DNA molecules

30
Q

How are extranuclear genes inherited?

A

Maternally - because the zygote’s cytoplasm comes from the egg