The transmission of traits from one generation to the next.
Differences between members of the same species.
The scientific study of heredity and hereditary variation.
A discrete unit of hereditary information consisting of a specific nucleotide sequence in DNA (or RNA, in some viruses).
The generation of offspring from a single parent that occurs without the fusion of gametes (by budding, division of a single cell, or division of the entire organism into two or more parts). In most cases, the offspring are genetically identical to the parent.
(1) A lineage of genetically identical individuals or cells. (2) In popular usage, a single individual organism that is genetically identical to another individual. (3) As a verb, to make one or more genetic replicas of an individual or cell. See also gene cloning.
any cell in multicellular organism except an egg or sperm
the union of gametes in fertilization
A display of the chromosome pairs of a cell arranged by size and shape.
chromosomes that are not directly involved in determining the sex of an individual
A cell containing only one set of chromosomes (n).
A cell containing two sets of chromosomes (2n), one set inherited from each parent.
A pair of chromosomes of the same length, centromere position, and staining pattern that possess genes for the same characters at corresponding loci. One homologous chromosome is inherited from the organism's father, the other from the mother. Also called homologs, or a homologous pair.
The diploid product of the union of haploid gametes in conception; a fertilized egg
alternation of generations
A life cycle in which there is both a multicellular diploid form, the sporophyte, and a multicellular haploid form, the gametophyte; characteristic of plants and some algae.
The pairing and physical connection of replicated homologous chromosomes during prophase I of meiosis.
A four-part structure that forms during the prophase of meiosis and consists of two homologous chromosomes, each composed of two sister chromatids.
The X-shaped, microscopically visible region where homologous nonsister chromatids have exchanged genetic material through crossing over during meiosis, the two homologs remaining associated due to sister chromatid cohesion.
The reciprocal exchange of genetic material between nonsister chromatids during prophase I of meiosis.
During meiosis the two separated partners of a chromosome pair are distributed randomly to the reproductive cells gametes, each gamete having an equal chance of receiving either chromosome
replicated homologous chromosomes pair and exchange segments
Chromosomes line up by homologous pairs
Each pair of homologous chromosomes separates
2 haploid cells form; each chromosome still consists of 2 sister chromatids