Module 3 Flashcards

1
Q

Chromatin

A

DNA + protein

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2
Q

P arm

A

Short arm

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3
Q

Q arm

A

Long arm

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4
Q

Heterochromatin

A

Stains dark, repetitive, noncoding DNA

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5
Q

Euchromatin

A

Stains light, protein coding regions

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6
Q

Telomeres

A

Tips of chromosomes, series of repeats

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7
Q

Gametes

A

Egg and sperm

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8
Q

Diploid

A

Somatic cells with two homologous sets of chromosomes

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9
Q

Haploid

A

Germline cells. Duplications through meiosis

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10
Q

Mitosis

A

Cell division where chromosomes duplicate and segregate to daughter cells

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11
Q

Prophase

A

Condense chromosomes

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12
Q

Metaphase

A

Line up chromosomes

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13
Q

Anaphase

A

Separate chromosomes

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14
Q

Telophase

A

Rebuild nuclear membranes

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15
Q

Meiosis

A

Process that reduces the number of chromosome sets from 2 to 1

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16
Q

Meiosis 1

A

Homologous pairs of chromosomes separate from each other

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17
Q

Meiosis 2

A

Sister chromatids separate from each other

18
Q

Prophase 1

A

Homologous recombination and crossing over

19
Q

Nondisjunction

A

Happens if the correct chromosomes do not pair during recombination

20
Q

Aneuploidy

A

Missing a single chromosome or has an extra one

21
Q

Maternal age effect

A

Nondisjunction and chromosomal abnormalities increase as women age

22
Q

Gregor Mendel

A

Discovered principles of genetics in experiments with garden pea

23
Q

Monohybrid cross

A

Followed a single trait or phenotype

24
Q

Dominance

A

One allele’s presence can mask the expression of the other allele

25
Q

Law of Segregation

A

Each person has two alleles from mom and dad. The phenotype depends on the genotype. An individual passes one allele to progeny

26
Q

Homozygous

A

Two identical alleles of a gene

27
Q

Heterozygous

A

Two different alleles of a gene

28
Q

Wild type allele

A

Most common form of an allele

29
Q

Wild type phenotype

A

Most common expression of an allele

30
Q

Mutant phenotype

A

Variant of a trait due to mutation in the allele

31
Q

`Punnett square

A

Used to calculate probability of outcomes of monohybrid cross

32
Q

Testcross

A

To cross an individual of unknown genotype to one that is known to be homozygous recessive

33
Q

Modes of inheritance

A

Explain common patterns of a single gene inheritance

34
Q

Pedigree

A

Charts that display family relationships and phenotypes

35
Q

Incomplete dominance

A

Neither allele is dominant over the other and expression of both is observed as a mix

36
Q

Codominance

A

Neither allele is dominant and both are expressed as a distinct phenotype

37
Q

Genetic heterogeneity

A

Mutations in different genes produce the same phenotype

38
Q

Pleiotropy

A

One gene influences expression of multiple phenotypes

39
Q

Epistasis

A

Gene masks the affect of another gene

40
Q

Penetrance

A

All or none expression of a genotype

41
Q

Expressivity

A

Severity of a phenotype