Sexual Reproduction and Inheritance

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Flashcards covering sex determination, meiosis, and inheritance.

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21 Terms

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Whole arm syndrome/heart hand syndrome

A condition where the thumb looks like a finger and there may be a massive atrial defect, often linked to the TBX5 gene.

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TBX5 Gene

A gene involved in the formation of both the thumb and the heart; its expression can be influenced by its environment.

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In Vitro Fertilization (IVF)

A procedure resulting from developmental biology advancements, now used by a significant percentage of couples.

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Fertilization

The process that activates the egg to begin development, restoring the diploid number of chromosomes.

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Zygote

The cell formed when the sperm nucleus migrates to the female pronucleus and creates a diploid nucleus.

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Diplotic

refers to sexual reproduction where two haploid gametes meet to form a diploid individual.

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SRY Region

The sex-determining region on the Y chromosome; without this gene, an individual cannot be male.

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Default State of vertebrate embryos

Female, unless overridden by the SRY gene.

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Wnt4

Activates DAX1 to make ovaries

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SOX9

Allows activation/development of testes.

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Thermosensitive Period

A period in some species (e.g., turtles) where temperature determines the sex of the offspring through the expression of SOX9.

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Main benefit of sexual reproduction

Variability due to meiosis, allowing for crossover events and unique combinations of genes.

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Meiosis

The process of cell division that separates homologous chromosomes and allows for genetic crossover, resulting in haploid cells.

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Crossing Over

The exchange of genetic information during meiosis, leading to recombinant chromatids and increased genetic variation.

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Recombination Frequency

The frequency at which crossover events occur, often used to create genetic maps; higher frequency means genes are further apart on the chromosome.

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Alfred Sturtevant

The scientist who first proposed using recombination frequency to map genes on a chromosome.

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Linked Genes

Genes located close together on a chromosome with a lower recombination frequency.

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X-linked Recessive Condition

A condition that manifests when there is a genetic variation on both X chromosomes (females) or a single X chromosome (males).

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X-linked Dominant Condition

A condition that manifests with a mutation on a single X chromosome.

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Hemizygous

Having only one copy of a gene or set of genes. This is used to describe males for genes on the X chromosome.

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Aneuploidy

An abnormal number of chromosomes, leading to conditions like trisomy 13 (Down syndrome) or missing chromosome structures.