Chromosomal Basis Of Inheritance Flashcards

1
Q

What is codominance?

A

Codominance is a type of inheritance where two different versions of a gene (alleles) are expressed equally and produce different traits in an organism.

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2
Q

What does homozygous mean?

A

Homozygous refers to an organism that has two identical copies of a particular gene.

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3
Q

What does heterozygous mean?

A

Heterozygous refers to an organism that has two different copies of a particular gene.

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4
Q

What is phenotype?

A

Phenotype is the observable characteristics or traits of an organism.

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5
Q

What is a polygenic trait?

A

A polygenic trait is a characteristic that is controlled by multiple genes.

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6
Q

What is pleiotropy?

A

Pleiotropy is the phenomenon where a single gene influences multiple, seemingly unrelated phenotypic traits within an organism.

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7
Q

What is epistasis?

A

Epistasis is a biological phenomenon that occurs when the expression of one or more genes modifies the expression of another gene.

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8
Q

What is a test cross?

A

A test cross is a cross with a homozygous recessive to determine the genotype of an unknown.

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9
Q

What is a dihybrid cross?

A

A dihybrid cross is a cross that involves two different gene pairs.

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10
Q

What is incomplete dominance?

A

Incomplete dominance is a pattern of inheritance where two alleles blend to create a new phenotype in the offspring.

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11
Q

How many pairs of Autosomes do humans have?

A

22 pairs of autosomes
Humans have one pair of sex chromosomes (XX female, XY male)

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12
Q

Nondisjunction

A

Failure of chromosomes to separate properly during meiosis, resulting in aneuploidy

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13
Q

Aneuploidy

A

Abnormal number of chromosomes (e.g.,monosomy, trisomy)

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14
Q

Monosomy
Trisomy

A

Monosomy: Missing one chromosome (2n - 1).

Trisomy: Extra chromosome (2n + 1).

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15
Q

Polyploidy

A

Organism has more than two complete sets of chromosomes

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16
Q

Sex linked traits

A

Traits associated with genes located on sex chromosomes

17
Q

What is Down Syndrome?

A

Down Syndrome (Trisomy 21) is caused by an extra copy of chromosome 21. It is associated with developmental delays, distinctive facial features, and varying levels of intellectual disability.

18
Q

What is Turner Syndrome?

A

Turner Syndrome (XO) occurs in females with only one X chromosome. It leads to short stature, infertility, and sometimes heart and developmental issues.

19
Q

What is Klinefelter Syndrome?

A

Klinefelter Syndrome (XXY) occurs in males with an extra X chromosome. Symptoms may include reduced testosterone levels, infertility, and some feminine physical traits.

20
Q

What is the Law of Segregation?

A

During meiosis, alleles for each gene separate so that each gamete carries only one allele for each gene.

21
Q

What is the Law of Independent Assortment?

A

Genes located on different chromosomes assort independently during gamete formation.

22
Q

What did Thomas Hunt Morgan’s experiments with fruit flies establish?

A

Morgan’s work established that genes are located on chromosomes and that some traits are sex-linked.

23
Q

What evidence did Morgan’s experiments provide?

A

His experiments provided evidence for linkage and crossing over.