Coilin Methylation Regulates Nuclear Body Formation
Developmental Cell, ISSN: 1534-5807, Vol: 3, Issue: 3, Page: 329-337
2002
- 151Citations
- 63Captures
- 5Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations151
- Citation Indexes150
- 150
- CrossRef138
- Policy Citations1
- 1
- Captures63
- Readers63
- 63
- Mentions5
- References5
- 5
Article Description
Cajal bodies (CBs) are nuclear suborganelles involved in biogenesis of small RNAs. Twin structures, called gems, contain high concentrations of the survival motor neurons (SMN) protein complex. CBs and gems often colocalize, and communication between these subdomains is mediated by coilin, the CB marker. Coilin contains symmetrical dimethylarginines that modulate its affinity for SMN, and, thus, localization of SMN complexes to CBs. Inhibition of methylation or mutation of the coilin RG box dramatically decreases binding of coilin to SMN, resulting in gem formation. Coilin is hypomethylated in cells that display gems, but not in those that primarily contain CBs. Likewise, extracts prepared from cells that display gems are less efficient in methylating coilin and Sm constructs in vitro. These results demonstrate that alterations in protein methylation status can affect nuclear organization.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1534580702002228; http://dx.doi.org/10.1016/s1534-5807(02)00222-8; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0036746771&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/12361597; http://linkinghub.elsevier.com/retrieve/pii/S1534580702002228; http://api.elsevier.com/content/article/PII:S1534580702002228?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:S1534580702002228?httpAccept=text/plain; https://linkinghub.elsevier.com/retrieve/pii/S1534580702002228; http://dx.doi.org/10.1016/s1534-5807%2802%2900222-8; http://www.cell.com/developmental-cell/abstract/S1534-5807(02)00222-8?_returnURL=http%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS1534580702002228%3Fshowall%3Dtrue; http://www.cell.com/article/S1534580702002228/abstract; http://www.cell.com/article/S1534580702002228/fulltext; http://www.cell.com/article/S1534580702002228/pdf
Elsevier BV
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