A novel variant in the 3′ UTR of human SCN1A gene from a patient with Dravet syndrome decreases mRNA stability mediated by GAPDH’s binding-Reference-Cited by-同舟云学术

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A novel variant in the 3′ UTR of human SCN1A gene from a patient with Dravet syndrome decreases mRNA stability mediated by GAPDH’s binding

Published:2014-01-25 Issue:6 Volume:133 Page:801-811
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Zeng Tao,Dong Zhao-Fei,Liu Shu-Jing,Wan Rui-Ping,Tang Ling-Jia,Liu Ting,Zhao Qi-Hua,Shi Yi-Wu,Yi Yong-Hong,Liao Wei-Ping,Long Yue-Sheng

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-014-1422-8.pdf

Reference59 articles.

1. Andreassi C, Riccio A (2009) To localize or not to localize: mRNA fate is in 3′ UTR ends. Trends Cell Biol 19:465–474

2. Backlund M, Paukku K, Daviet L, De Boer RA, Valo E, Hautaniemi S, Kalkkinen N, Ehsan A, Kontula KK, Lehtonen JY (2009) Posttranscriptional regulation of angiotensin II type 1 receptor expression by glyceraldehyde 3-phosphate dehydrogenase. Nucl Acids Res 37:2346–2358

3. Bough KJ, Rho JM (2007) Anticonvulsant mechanisms of the ketogenic diet. Epilepsia 48:43–58

4. Chatterjee S, Pal JK (2009) Role of 5′- and 3′-untranslated regions of mRNAs in human diseases. Biol Cell 101:251–262

5. Chen JM, Ferec C, Cooper DN (2006) A systematic analysis of disease-associated variants in the 3′ regulatory regions of human protein-coding genes I: general principles and overview. Hum Genet 120:1–21

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