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Sticky mouse

From Wikipedia, the free encyclopedia

Sticky mouse is a murine possessing a gene mutation in the enzyme alanyl-tRNA synthetase (AARS).[1] The sticky mouse, with this particular mutation, presents a good model in which to investigate mechanisms of neuronal degeneration. Its most immediately obvious symptom is a sticky secretion on the mouse's fur (thus the name); however, it is accompanied by lack of muscle control, ataxia, alopecia, loss of Purkinje cells in the cerebellum, and eventually, death.

Sticky mouse is one of several animal mutants that are known to have problems in mRNA translation and are used in studies.[2].

A genetic mutation affecting the laminin α2 chain has been characterized in mouse models generated through targeted disruption of the Lama2 gene. These mutant mice exhibit severe muscular dystrophy, growth retardation, and early postnatal death. The absence of laminin α2 leads to progressive muscle fiber degeneration associated with increased apoptotic activity.[3]

See also

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References

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  1. Roy H, Ibba M (September 2006). "Molecular biology: sticky end in protein synthesis". Nature. 443 (7107): 41–2. Bibcode:2006Natur.443...41R. doi:10.1038/nature05002. PMID 16906138. S2CID 5998660.
  2. Scheper GC, van der Knaap MS, Proud CG (September 2007). "Translation matters: protein synthesis defects in inherited disease". Nat. Rev. Genet. 8 (9): 711–23. doi:10.1038/nrg2142. PMID 17680008. S2CID 12153982.
  3. Miyagoe Y, Hanaoka K, Nonaka I, Hayasaka M, Nabeshima Y, Arahata K, Takeda S (September 22, 1997). "Laminin alpha2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophy". FEBS Letters. 415 (1): 33–39. doi:10.1016/S0014-5793(97)01007-7. PMID 9326364.
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