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MutSβ abundance and Msh3 ATP hydrolysis activity are important drivers of CTG•CAG repeat expansions

CTG•CAG repeat expansions cause at least twelve inherited neurological diseases. Expansions require the presence, not the absence, of the mismatch repair protein MutSβ (Msh2-Msh3 heterodimer). To evaluate properties of MutSβ that drive expansions, previous studies have tested under-expression, ATPas...

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Bibliografski detalji
Izdano u:Nucleic Acids Res
Glavni autori: Keogh, Norma, Chan, Kara Y., Li, Guo-Min, Lahue, Robert S.
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2017
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5622409/
https://ncbi.nlm.nih.gov/pubmed/28973443
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkx650
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