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These flashcards cover the key vocabulary and concepts for Chapter 9, including the mechanisms of meiosis, genetic variation, and chromosomal disorders resulting from nondisjunction.
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Ploidy
The number of complete sets of chromosomes in a cell; for example, animals are mostly diploid while asexually reproducing organisms are haploid.
Diploid
Cells or organisms containing two homologous sets of chromosomes (2n), with one set inherited from each parent.
Haploid
Cells or organisms containing only a single set of chromosomes (1n), typical of asexually reproducing organisms and gametes.
Homologous chromosomes
Pairs of chromosomes that are the same size, have the same centromere position, and carry the same genes, though they may have different alleles.
Alleles
Variations or different versions of a single gene.
Somatic cells
All body cells except for gametes; these cells are diploid (2n) and divide via mitosis.
Gametes
Sex cells (sperm and egg cells) that are haploid (1n) and genetically unique, produced through meiosis.
Mitosis
Somatic cell division that produces two genetically identical daughter cells for the purpose of growth and repair.
Meiosis
Sex cell division in germ cells where DNA replicates once but the nucleus divides twice, yielding four genetically unique haploid gametes.
Fertilization
The process where a haploid sperm (1n) fuses with a haploid egg (1n) to form a diploid zygote (2n).
Zygote
A single-cell fertilized egg that contains 46 chromosomes in 23 pairs in humans.
Germ cells
Specialized cells that undergo meiosis to produce haploid gametes.
Interphase
The phase of the cell cycle preceding division where the cell grows and copies its DNA; it includes G1, S (DNA synthesis), and G2 stages.
Crossing-over
Also known as recombination; a process during Prophase I where homologous chromosome pairs exchange genetic material, giving rise to greater allele variations.
Recombinant chromatid
A chromatid produced by the process of crossing over that contains a new combination of maternal and paternal genetic information.
Random assortment
Also known as independent assortment; the process during Metaphase I where homologous chromosome pairs align independently and randomly at the metaphase plate.
Random fertilization
A source of genetic diversity where any sperm can fuse with any egg, resulting in approximately 223 combinations per gamete and about 1 in 70 trillion total possible combinations.
Monozygotic twins
Identical twins formed from a single zygote that splits into two embryos.
Dizygotic twins
Fraternal twins formed when two separate eggs are fertilized by two different sperm, resulting in two distinct zygotes.
Nondisjunction
An error in meiosis, most common in Meiosis I, where chromosomes fail to separate properly, leading to gametes with extra or missing chromosomes.
Aneuploidy
A condition characterized by an atypical chromosome number, such as having one extra (n+1) or one missing (n−1) chromosome.
Monosomic
A type of aneuploidy where a cell is missing a chromosome, represented as (n−1).
Trisomic
A type of aneuploidy where a cell has an extra chromosome, represented as (n+1); examples include Trisomy 21 and Trisomy 18.
Turner syndrome
A sex chromosome abnormality with the genotype XO, occurring in approximately 1 in 2000 females, characterized by short stature and infertility.
Klinefelter syndrome
A sex chromosome abnormality with the genotype XXY, occurring in approximately 1 in 750 males, characterized by tall stature and breast development.
Polyploidy
A condition where an organism has extra complete sets of chromosomes (e.g., 3n, 4n, 8n). While fatal in humans, it is common and often beneficial in plants like bananas and strawberries.