ch 15 Genetics and Inheritance Concepts

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These flashcards cover key vocabulary and concepts related to genetics and inheritance as presented in the lecture notes.

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40 Terms

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Tay-Sachs disease

A genetic disorder caused by a mutation in the HEXA gene that leads to the destruction of nerve cells in the brain and spinal cord.

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Mendel’s Law of Independent Assortment

One gene does not affect the inheritance of another gene. Genes on different chromosomes will separate during meiosis independently

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Thomas Morgan Hunt

Who found the first solid evidence associating a specific gene with a specific chromosome?

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Drosophila melanogastar (fruit fly)

What species did Morgan start to study?

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Wild type

______ aka normal phenotypes that are common in population

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Genetic recombination

_________ is the production of offspring wit combinations of traits different from either parent

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Genetic map

________ is an ordered list of genetic loci along a particular chromosome

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What did Strurtvant predict with the genetic map?

The farther part two genes are, the higher probability that a crossover will occur between them aka the higher the recombination frequency

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Linkage map

_______ is a genetic map of chromosomes based on recombination frequencies

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Map units

Distance between genes can be expressed as ______

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1% recombination frequency

What does one map unit represent on a linkage map?

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Separated/unlinked

What does it mean if there are at least 50 map units between two genes?

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Turner syndrome (X)

What condition is a result of having only one sex chromosome: X0

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Klinefelter Syndrome

What condition is a result of having an extra X chromosome (XXY)

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Jacob’s Syndrome (super males)

What condition is a result of an extra Y chromosome (XYY)

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Meta females

What is the condition of having three X chromosomes?

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Polyploidy

What condition in which an organism has more than two complete sets of chromosomes such as triploidy (3n) and tetraploidy (4n)

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What is polyploidy common in?

Plants

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Breakage of a chromosome can lead to four types of changes in a chromosome:

Deletion, duplication, inversion, translocation

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Deletion

_____ is the removal of a chromosomal fragment

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Duplication

______ repeats a segment on a chromosome

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Inversion

______ reverses orientation of a segment within a chromosome

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Translocation

______ moves a segment from one chromosome to another

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cri du chat (cry of the cat)

The syndrome ______ results from a deletion in chromosome 5 that usually die early in childhood

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Mitochondrial myopathy

_________ is defects in mitochondrial genes that prevents cells from making enough ATP

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Methylation

______ is the addition of methyl group that binds to histones

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Acetylation

______ is the addition of an acetyl group to active genes nearby to loosen up DNA to activate genes

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Mutant phenotypes

______ are traits alternative to the wild type

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SRY

A gene on the Y chromosome aka _____ is responsible for the development of the testes

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Sex linked gene

A gene that is located on either sex chromosome is called _______

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Homozygous dominant/recessive

What combination of alleles are needed for a testcross?

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Autosomal recessive trait

A trait that is expressed only when two copies of the recessive allele are present.

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Law of Segregation

Mendelian principle that states that each individual has two alleles for each gene and that these alleles segregate during gamete formation.

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Dihybrid cross

A genetic cross between individuals that differ in two traits, examining the inheritance patterns of both.

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Independent assortment

Mendel’s second law, stating that genes for different traits can segregate independently during the formation of gametes.

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Genetic linkage

Tendency of alleles that are located close to each other on a chromosome to be inherited together.

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X-linked inheritance

Pattern of inheritance characteristic of genes located on the X chromosome, often resulting in different patterns of disease manifestation in males and females.

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Aneuploidy

A condition in which an individual has an abnormal number of chromosomes, which can lead to various genetic disorders.

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Linkage map

A genetic map based on recombination frequencies that shows the relative positions of genes on a chromosome.

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Barr body

The inactive X chromosome present in female mammals, which condenses to prevent gene expression.