Chapter 11 inheritance Flashcards

1
Q

Inheritance

A

is the process by which the traits of organisms are passed to their offspring.

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2
Q

alleles

A

are slightly different nucleotide sequences of a gene in a certain species. as per a result of a mutation or error in replicating DNA.

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3
Q

mutations

A

changes in the sequence of nucleotides in the DNA of a gene. If a mu- tation occurs in a cell that becomes a sperm or egg, it can be passed on from parent to offspring. all alelles originated as mutations and were passed down generations.

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4
Q

If both homologues have the same allele at a given

gene locus, the organism is said to be

A

homozygous

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5
Q

If two homologous chromosomes have different alleles at a locus, the organism is _____ (“different pair”) at that locus.

A

heterozygous

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6
Q

genotype

A

the genetic composition of an organism: the actual alleles of each gene carried by the organism

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7
Q

phenotype

A

the physical characteristics of an organism; can be defined as outward appearance, behaviour or molecular characteristics

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8
Q

dominant

A

an allele that can determine the phenotype of heterozygotes so that they are indistinguishable from individuals homozygous for that allele. The expression of the other, recessive allele is completely masked

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9
Q

recessive

A

an allele that is expressed only in homozygotes and is completely masked in heterozygotes in the presence of a dominant allele

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10
Q

howdid Mendel’s experimentscontributed to our understanding of inheritance of a single gene.

A

Mendel discovered the fundamental laws of inheritance. He deduced that genes come in pairs and are inherited as distinct units, one from each parent. Mendel tracked the segregation of parental genes and their appearance in the offspring as dominant or recessive traits.

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11
Q

segregation

A

the process in eukaryotes by which two sister chromatids formed as a consequence of DNA replication, or paired homologous chromosomes, separate from each other and migrate to opposite poles of the nucleus. This process occurs during both mitosis and meiosis.

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12
Q

Autosomes:

A

a chromosome that occurs in homologous pairs in both males and females and that does not bear the genes determining sex

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13
Q

Independent assortment:

A

where the alleles of two (or more) different genes get sorted into gametes independently of one another; they are not linked

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14
Q

Punnet square:

A

a method of predicting the genotype and phenotype of offspring in genetic crosses

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15
Q

Test cross:

A

a breeding experiment in which an individual showing the dominant phenotype is mated with an individual that is homozygous is recessive for the same gene.

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16
Q

Incomplete dominance:

A

a pattern of inheritance in which the heterozygous phenotype is intermediate between the two homozygous phenotypes

17
Q

Pleiotropy:

A

the situation in which a single gene influences more than one phenotypical characteristic

18
Q

Sex-linked:

A

referring to a pattern of inheritance characteristic of genes located on one type of sex chromosome and not found on the other type. For instance in X linked inheritance, females show the dominant trait unless they are homozygous recessive, whereas males express whichever allele, dominant or recessive is found on their X chromosome