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  2. Chromosomal translocation - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_translocation

    In genetics, chromosome translocation is a phenomenon that results in unusual rearrangement of chromosomes. This includes balanced and unbalanced translocation, with two main types: reciprocal, and Robertsonian translocation. Reciprocal translocation is a chromosome abnormality caused by exchange of parts between non-homologous chromosomes.

  3. Non-homologous end joining - Wikipedia

    en.wikipedia.org/wiki/Non-homologous_end_joining

    Non-homologous end joining (NHEJ) is a pathway that repairs double-strand breaks in DNA. It is called "non-homologous" because the break ends are directly ligated without the need for a homologous template, in contrast to homology directed repair (HDR), which requires a homologous sequence to guide repair. NHEJ is active in both non-dividing ...

  4. Robertsonian translocation - Wikipedia

    en.wikipedia.org/wiki/Robertsonian_translocation

    When these chromosomes break at their centromeres, the two resulting long arms may fuse. The result is a single, large chromosome with a metacentric centromere. This form of rearrangement is a Robertsonian translocation. [citation needed] This type of translocation may involve homologous (paired) or non-homologous chromosomes. Owing to the ...

  5. Nondisjunction - Wikipedia

    en.wikipedia.org/wiki/Nondisjunction

    Note that chromosome 21 is present in 3 copies, while all other chromosomes show the normal diploid state with 2 copies. Most cases of trisomy of chromosome 21 are caused by a nondisjunction event during meiosis I (see text). Down syndrome, a trisomy of chromosome 21, is the most common anomaly of chromosome number in humans. [2]

  6. Meiosis - Wikipedia

    en.wikipedia.org/wiki/Meiosis

    However, a subset of breaks (at least one per chromosome) form crossovers between non-sister (homologous) chromosomes resulting in the exchange of genetic information. [25] The exchange of information between the homologous chromatids results in a recombination of information; each chromosome has the complete set of information it had before ...

  7. Homologous chromosome - Wikipedia

    en.wikipedia.org/wiki/Homologous_chromosome

    Homologous chromosomes are made up of chromosome pairs of approximately the same length, centromere position, and staining pattern, for genes with the same corresponding loci. One homologous chromosome is inherited from the organism's mother; the other is inherited from the organism's father. After mitosis occurs within the daughter cells, they ...

  8. Illegitimate recombination - Wikipedia

    en.wikipedia.org/wiki/Illegitimate_Recombination

    Non-homologous end joining a process of illegitimate recombination versus a homology driven recombination event. Illegitimate recombination, or nonhomologous recombination, is the process by which two unrelated double stranded segments of DNA are joined. This insertion of genetic material which is not meant to be adjacent tends to lead to genes ...

  9. Chromosomal crossover - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_crossover

    Chromosomal crossover, or crossing over, is the exchange of genetic material during sexual reproduction between two homologous chromosomes ' non-sister chromatids that results in recombinant chromosomes. It is one of the final phases of genetic recombination, which occurs in the pachytene stage of prophase I of meiosis during a process called ...