Nondisjunction
Say it: non-dis-JUNGK-shun
Nondisjunction is the failure of paired chromosomes or sister chromatids to separate in cell division, leaving cells with the wrong chromosome number.
Also: non-disjunction
Definition
What is nondisjunction?
Nondisjunction is an error of cell division in which chromosomes that should move to opposite poles of the cell travel to the same pole instead. It can happen in meiosis I, when a pair of homologous chromosomes stays together, or in meiosis II or mitosis, when two sister chromatids fail to part. One daughter cell then ends up with an extra copy of the chromosome and the other with none.
If nondisjunction occurs as eggs or sperm form, a human gamete may carry 24 or 22 chromosomes instead of 23, and an embryo formed from it has a gain or loss of a whole chromosome in every cell, a state called aneuploidy. A gain gives trisomy, as in Down syndrome (three copies of chromosome 21), and a loss gives monosomy, as in Turner syndrome (a single X chromosome). Most other autosome gains or losses end in miscarriage, while extra or missing sex chromosomes are better tolerated. An error in meiosis I makes all four products abnormal, while an error in meiosis II leaves two of the four normal.
The chance of nondisjunction in eggs rises with the mother's age, which is why the likelihood of trisomy 21 increases in later pregnancies. Nondisjunction during mitosis after fertilization produces mosaicism, in which only some of a person's cells have an abnormal number.
Word parts
Where does the word “nondisjunction” come from?
- non-
- notLatin non
- disjunction
- a separating, an unyokingLatin disiunctio, from dis- (apart) and iungere (to join)
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Terms that go with it
- MeiosisMeiosis is a two-stage cell division that turns one diploid cell into four genetically different haploid cells, the precursors of eggs and sperm.
- KaryotypeA karyotype is the full set of chromosomes in a cell, or a picture of them sorted into pairs, used to check chromosome number and structure.
- ChromosomeA chromosome is a thread-like structure of DNA and protein that carries an organism's genes; most human cells hold 46 of them in 23 pairs.
- GameteA gamete is a haploid reproductive cell, such as a sperm or an egg, that fuses with a gamete of the opposite type at fertilization to form a zygote.
- CentromereA centromere is the constricted region of a chromosome where its two sister chromatids are held together and where spindle fibers attach in cell division.
- MitosisMitosis is the division of a cell's nucleus that gives each of two daughter cells an identical, complete set of chromosomes.
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Checked against
Written for biofideX in plain words, after checking these references:
- OpenStax Biology 2e, 13.2 Chromosomal Basis of Inherited Disorders
- NCBI MeSH: Nondisjunction, Genetic
- MedlinePlus Genetics: Can changes in the number of chromosomes affect health and development?
- NHGRI Talking Glossary: Aneuploidy
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