From Wikipedia, the free encyclopedia
(Redirected from Sticky mouse syndrome)

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]

See also

References

  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.


From Wikipedia, the free encyclopedia
(Redirected from Sticky mouse syndrome)

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]

See also

References

  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.



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