V体育官网入口 - Elevated FMR1 mRNA in premutation carriers is due to increased transcription
- PMID: 17283214
- PMCID: PMC1831862
- DOI: 10.1261/rna.280807
Elevated FMR1 mRNA in premutation carriers is due to increased transcription
VSports最新版本 - Abstract
Carriers of premutation alleles (55-200 CGG repeats) of the fragile X mental retardation 1 (FMR1) gene have levels of FMR1 mRNA that are elevated by as much as 10-fold in peripheral blood leukocytes and CNS tissue. The excess expanded-repeat mRNA, per se, is now believed to result in forms of clinical involvement that are largely restricted to premutation carriers, including the neurodegenerative disorder, fragile X-associated tremor/ataxia syndrome (FXTAS). Although evidence to date suggests that the elevated mRNA is not due to increased stability, the basis for the increase is not known. In the current study, we have determined the relative transcriptional activities of premutation and normal FMR1 alleles using a highly sensitive nuclear run-on assay that involves immunocapture of digoxigenin-modified run-on transcripts followed by PCR amplification of the nascent transcripts. Using the nuclear run-on approach, we demonstrate that the rate of run-on synthesis of FMR1 transcripts is increased in premutation alleles. The current run-on assay should be broadly applicable to studies of other genes with promoters of weak to moderate strength. The fraction of capped FMR1 mRNA remains unaltered for premutation transcripts, indicating that elevated message levels are not due to premature escape from the cotranscriptional capping process. We also show that, in contrast to the situation with myotonic dystrophy, there is no net nuclear sequestration of premutation FMR1 mRNA. Finally, we have demonstrated that AGG interruptions within the CGG repeat element do not influence FMR1 mRNA levels. VSports手机版.
"V体育官网" Figures
References
-
- Allen, E.G., He, W., Yadav-Shah, M., Sherman, S.L. A study of the distributional characteristics of FMR1 transcript levels in 238 individuals. Hum. Genet. 2004;114:439–447. - PubMed (V体育官网入口)
-
- Allingham-Hawkins, D.J., Babul-Hirji, R., Chitayat, D., Holden, J.J., Yang, K.T., Lee, C., Hudson, R., Gorwill, H., Nolin, S.L., Glicksman, A., et al. Fragile X premutation is a significant risk factor for premature ovarian failure: The International Collaborative POF in Fragile X study–preliminary data. Am. J. Med. Genet. 1999;83:322–325. - PMC - PubMed
-
- Arocena, D.G., Iwahashi, C.K., Won, N., Beilina, A., Ludwig, A.L., Tassone, F., Schwartz, P.H., Hagerman, P.J. Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells. Hum. Mol. Genet. 2005;14:3661–3671. - PubMed (V体育安卓版)
-
- Beilina, A., Tassone, F., Schwartz, P.H., Sahota, P., Hagerman, P.J. Redistribution of transcription start sites within the FMR1 promoter region with expansion of the downstream CGG-repeat element. Hum. Mol. Genet. 2004;13:543–549. - PubMed (VSports最新版本)
-
- Chen, L.S., Tassone, F., Sahota, P., Hagerman, P.J. The (CGG)n repeat element within the 5′ untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter. Hum. Mol. Genet. 2003;12:3067–3074. - PubMed
Publication types
- "VSports最新版本" Actions
MeSH terms
- V体育平台登录 - Actions
- VSports在线直播 - Actions
- "VSports手机版" Actions
- VSports最新版本 - Actions
Substances (V体育ios版)
Grants and funding
"VSports" LinkOut - more resources
Full Text Sources
Other Literature Sources
"VSports手机版" Medical