4.5 Article

Evidence of nuclei-encoded spliceosome mediating splicing of mitochondrial RNA

期刊

HUMAN MOLECULAR GENETICS
卷 26, 期 13, 页码 2472-2479

出版社

OXFORD UNIV PRESS
DOI: 10.1093/hmg/ddx142

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资金

  1. California Institute for Regenerative Medicine (CIRM) [DISC1-08825, TR2-01814, TR4-06747]
  2. National Institutes of Health [R01MH108528, R01MH109885, R01MH100175, R21MH107771, R56MH109587, R01MH094753, R01MH103134, U19MH107367, P01NICHD033113]
  3. National Alliance for Research on Schizophrenia and Depression (NARSAD) Independent Investigator Grant
  4. International Rett Syndrome Foundation (IRSF) [2925]

向作者/读者索取更多资源

Mitochondria are thought to have originated as free-living prokaryotes. Mitochondria organelles have small circular genomes with substantial structural and genetic similarity to bacteria. Contrary to the prevailing concept of intronless mitochondria, here we present evidence that mitochondrial RNA transcripts (mtRNA) are not limited to policystronic molecules, but also processed as nuclei-like transcripts that are differentially spliced and expressed in a cell-type specific manner. The presence of canonical splice sites in the mtRNA introns and of core components of the nuclei-encoded spliceosome machinery within the mitochondrial organelle suggest that nuclei-encoded spliceosome can mediate splicing of mtRNA.

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