4.3 Article

RNA editing of the Q/R site of GluA2 in different cultured cell lines that constitutively express different levels of RNA editing enzyme ADAR2

期刊

NEUROSCIENCE RESEARCH
卷 73, 期 1, 页码 42-48

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.neures.2012.02.002

关键词

AMPA receptor; GluA2; RNA editing; Adenosine deaminase acting on RNA type 2 (ADAR2); Splicing; Amyotrophic lateral sclerosis (ALS)

资金

  1. Ministry of Health, Labor, and Welfare of Japan [H18-Kokoro-017]
  2. Ministry of Education, Culture, Sports, Science, and Technology of Japan [18023012, 23590113]
  3. Grants-in-Aid for Scientific Research [23790977, 23791002, 23590113, 18023012] Funding Source: KAKEN

向作者/读者索取更多资源

Adenosine deaminase acting on RNA 2 (ADAR2) catalyzes RNA editing at the glutamine/arginine (Q/R) site of GluA2, and an ADAR2 deficiency may play a role in the death of motor neurons in ALS patients. The expression level of ADAR2 mRNA is a determinant of the editing activity at the GluA2 Q/R site in human brain but not in cultured cells. Therefore, we investigated the extent of Q/R site-editing in the GluA2 mRNA and pre-mRNA as well as the ADAR2 mRNA and GluA2 mRNA and pre-mRNA levels in various cultured cell lines. The extent of the GluA2 mRNA editing was 100% except in SH-SY5Y cells, which have a much lower level of ADAR2 than the other cell lines examined. The ADAR2 activity at the GluA2 pre-mRNA Q/R site correlated with the ADAR2 mRNA level relative to the GluA2 pre-mRNA. SH-SY5Y cells expressed higher level of the GluA2 mRNA in the cytoplasm compared with other cell lines. These results suggest that the ADAR2 expression level reflects editing activity at the GluA2 Q/R site and that although the edited GluA2 pre-mRNA is readily spliced, the unedited GluA2 pre-mRNA is also spliced and transported to the cytoplasm when ADAR2 expression is low. (c) 2012 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.

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