4.8 Article

Jmjd6 Catalyses Lysyl-Hydroxylation of U2AF65, a Protein Associated with RNA Splicing

期刊

SCIENCE
卷 325, 期 5936, 页码 90-93

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1175865

关键词

-

资金

  1. Glasstone Fellowship
  2. Deutsche Forschungsgemeinschaft [BO1748-3, LE2130/2-1]
  3. UK Biotechnology and Biological Sciences Research Council
  4. European Union
  5. Wellcome Trust
  6. Biotechnology and Biological Sciences Research Council [BB/D011523/1] Funding Source: researchfish
  7. Medical Research Council [G9826944] Funding Source: researchfish
  8. BBSRC [BB/D011523/1] Funding Source: UKRI
  9. MRC [G9826944] Funding Source: UKRI

向作者/读者索取更多资源

The finding that the metazoan hypoxic response is regulated by oxygen-dependent posttranslational hydroxylations, which regulate the activity and lifetime of hypoxia-inducible factor (HIF), has raised the question of whether other hydroxylases are involved in the regulation of gene expression. We reveal that the splicing factor U2 small nuclear ribonucleoprotein auxiliary factor 65-kilodalton subunit (U2AF65) undergoes posttranslational lysyl-5-hydroxylation catalyzed by the Fe(II) and 2-oxoglutarate-dependent dioxygenase Jumonji domain-6 protein (Jmjd6). Jmjd6 is a nuclear protein that has an important role in vertebrate development and is a human homolog of the HIF asparaginyl-hydroxylase. Jmjd6 is shown to change alternative RNA splicing of some, but not all, of the endogenous and reporter genes, supporting a specific role for Jmjd6 in the regulation of RNA splicing.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据