Myogenin: Difference between revisions
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==References== |
==References== |
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YOUR MUM |
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==Further reading== |
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Revision as of 11:16, 7 May 2008
Myogenin (myogenic factor 4), also known as MYOG, is a human gene.[5]
References
YOUR MUM
- ^ a b c GRCh38: Ensembl release 89: ENSG00000122180 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000026459 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: MYOG myogenin (myogenic factor 4)".
Further reading
Myogenin is a basic-helix-loop-helix (bHLH) transcription factor expressed during the development, maintenance, and repair of skeletal muscle. Myogenin belongs to the MyoD family of bHLH transcription factors, which also include MyoD, Myf5, and MRF4.[1] In particular, it is a myogenic regulatory factor (MRF). When the DNA coding for myogenin was knocked out of the mouse genome, severe skeletal muscle defects were observed. Mice lacking both copies of myogenin (homozygous-null) suffer from perinatal lethality due to the lack of mature secondary skeletal muscle fibers throughout the body.[2]
somite -----(myoD/myf5)------> myoblast -----(myogenin/MRF4)------> myotube
References
- ^ Sabourin LA, Rudnicki MA (2000). "The molecular regulation of myogenesis". Clin. Genet. 57 (1): 16–25. doi:10.1034/j.1399-0004.2000.570103.x. PMID 10733231.
- ^ Hasty P, Bradley A, Morris JH, Edmondson DG, Venuti JM, Olson EN, Klein WH (1993). "Muscle deficiency and neonatal death in mice with a targeted mutation in the myogenin gene". Nature. 364 (6437): 501–6. doi:10.1038/364501a0. PMID 8393145.
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External links
- Myogenin at the U.S. National Library of Medicine Medical Subject Headings (MeSH)