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Deletion (genetics)

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Deletion on a chromosome

In genetics, a deletion (also called gene deletion, deficiency, or deletion mutation) is a mutation (a genetic aberration) in which a part of a chromosome or a sequence of DNA is missing. Deletion is the loss of genetic material. Any number of nucleotides can be deleted, from a single base to an entire piece of chromosome.^[1] Deletions can be caused by errors in chromosomal crossover during meiosis. This causes several serious genetic diseases.

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[edit] Causes

Causes include the following:

Losses from translocation
Chromosomal crossovers within a chromosomal inversion
Unequal crossing over
Breaking without rejoining

For synapsis to occur between a chromosome with a large intercalary deficiency and a normal complete homolog, the unpaired region of the normal homolog must loop out of the linear structure into a deletion or compensation loop.

[edit] Types

Types of deletion include the following:

Terminal Deletion - a deletion that occurs towards the end of a chromosome.
Intercalary Deletion - a deletion that occurs from the interior of a chromosome.

[edit] Effects

Small deletions are less likely to be fatal; large deletions are usually fatal - but always, there is variation based on what genes are lost. Some medium-sized deletions lead to recognizable human disorders.

Deletion of a number of base pairs that is not evenly divisible by three will lead to a frameshift mutation, causing all of the codons occurring after the deletion to be read incorrectly during translation, producing a severely altered and potentially nonfunctional protein.

Deletions are responsible for an array of genetic disorders, including some cases of male infertility and two thirds of cases of Duchenne muscular dystrophy.^[1] A deletion of part of the short arm of chromosome 5 results in a syndrome called Cri du chat,^[1] also known as "cry of the cat" syndrome. It is found in approximately 1 in 50,000 live births. The surviving infants have a distinctive cry, severe mental retardation, and shortened life span.

[edit] See also

[edit] Reference

^ ^a ^b ^c Lewis R. 2005. Human Genetics: Concepts and Applications, 6th Ed. McGraw Hill, New York.

[hide] v • d • e Pathology: chromosome abnormalities (Q90-Q99, 758)
Autosomal trisomies	Down syndrome (21), Edwards syndrome (18), Patau syndrome (13), Trisomy 9, Warkany syndrome 2 (8), Cat eye syndrome (22)
Autosomal monosomies/deletions	Wolf-Hirschhorn syndrome (4), Cri du chat (5), Angelman syndrome/Prader-Willi syndrome (15)
X/Y linked	Turner syndrome, Triple X syndrome, Klinefelter's syndrome, XYY syndrome
Translocations	Philadelphia chromosome, Burkitt's lymphoma

Deletion (genetics)

Tuesday, August 28, 2007