Chapter 3.4 Inheritance Flashcards

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1
Q

Mendel

A

discovered the principles of inheritance with experiments in which large numbers of pea plants were crossed

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2
Q

Genotype

A

the symbolic representation of the pair of alleles possessed by an organism, typically represented by two letters ex: Bb, GG, tt

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3
Q

Phenotype

A

the characteristics or traits of an organism. ex: 5 fingers on each hand, colour blindness, type O blood.

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4
Q

Dominant allele

A

An allele that has the same effect on the phenotype whether it is paired with the same allele or a different one. Dominant alleles are always expressed in the phenotype
ex: the genotype Aa gives the dominant A trait because the a allele is masked, the a allele is not transcribed or translated during protein synthesis

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5
Q

Recessive allele

A

an allele that has an effect on the phenotype only when present in the homozygous state. ex: aa gives rise to the recessive trait because no dominant allele is there to mask it.

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6
Q

Co-dominant alleles

A

pairs of alleles that both affect the phenotype when present in a heterozygote. ex: a parent with curly hair and a parent with strait can have children with different degrees of hair curliness, because both alleles influence hair condition when both are present in the genotype.

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7
Q

Locus

A

the particular position on homologous chromosomes of a gene. Each gene is found at a specific place on a specific pair of chromosomes

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8
Q

Homozygous

A

having two identical alleles of a gene. ex: AA is a genotype that is homozygous dominant, whereas aa is the genotype of someone who is homozygous recessive for that trait.

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9
Q

Heterozygous

A

Having two different alleles of a gene. This results from the fact that the paternal allele is different from the maternal one. ex: Aa is a heterozygous genotype

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10
Q

Carrier

A

An individual who has a recessive allele of a gene that does not have an effect on the phenotype. ex: Aa carries the gene for albinism but has pigmented skin, which means an ancestor must have been albino and some offspring might be albino; if both parents are unaffected by a recessive condition yet both are carriers, some of their offspring could be affected.

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11
Q

Test cross

A

Testing a suspected heterozygote plant or animal by crossing it with known homozygous recessive (aa). Because a recessive allele can be masked, it is often impossible to tell whether an organism is AA or Aa unless they produce offspring that have the recessive trait. An example of a test cross is shown later in this section when we explore three generations of pea plants.

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12
Q

Punnett grid

A

to show all the possible combinations of genetic information for a particular trait in a monohybrid cross. A monohybrid cross is one in which the parents have different alleles and which shows the results for only one trait.

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13
Q

Autosomal Recessive Diseases

A

Diseases caused by recessive alleles and the locus of their gene is found on one of the first 22 pairs of chromosomes but not on the sex chromosomes X and Y. (albinism, cystic fibrosis, sickle cell disease, phenylketonuria, Tay Sachs disease, Thalassemia)

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14
Q

Sex Linked genetic trait

A

genetic trait whose gene has its locus on the X or the Y chromosome. Often genetic traits that show sex linkage affect one sex more than the other: Color Blindness and Hemophilia.

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15
Q

Haemophilia

A

a disorder in which blood does not clot properly.

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