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Point mutation in mitochondrial tRNA gene is associated with polycystic ovary syndrome and insulin resistance.

Abstract
Polycystic ovarian syndrome (PCOS) is characterized by chronic anovulation, hyperandrogenism and polycystic ovaries. To date, the molecular mechanisms underlying PCOS have remained to be fully elucidated. As recent studies have revealed a positive association between mitochondrial dysfunction and PCOS, current investigations focus on mutations in the mitochondrial genome of patients with POCS. The present study reported a Chinese patient with PCOS. Sequence analysis of the mitochondrial genome showed the presence of homoplasmic ND5 T12338C and tRNASer (UCN) C7492T mutations as well as a set of polymorphisms belonging to the human mitochondrial haplogroup F2. The T12338C mutation is known to decrease the ND5 mRNA levels and to inhibit the processing of RNA precursors. The C7492T mutation, which occurred at the highly conserved nucleotide in the anticodon stem of the tRNASer (UCN) gene, is important for the tRNA steady‑state level as well as the aminoacylation ability. Therefore, the combination of the ND5 T12338C and tRNASer (UCN) C7492T mutations may lead to mitochondrial dysfunction, and is likely to be involved in the pathogenesis of PCOS. The present study provided novel insight into the molecular mechanisms of PCOS.
AuthorsYu Ding, Guangchao Zhuo, Caijuan Zhang, Jianhang Leng
JournalMolecular medicine reports (Mol Med Rep) Vol. 13 Issue 4 Pg. 3169-72 (Apr 2016) ISSN: 1791-3004 [Electronic] Greece
PMID26935780 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Codon
  • Mitochondrial Proteins
  • RNA Precursors
  • RNA, Messenger
  • RNA, Transfer
  • MT-ND5 protein, human
  • Electron Transport Complex I
Topics
  • Adult
  • Animals
  • Base Sequence
  • Codon
  • Electron Transport Complex I (genetics, metabolism)
  • Female
  • Humans
  • Insulin Resistance
  • Mitochondria (genetics)
  • Mitochondrial Proteins (genetics, metabolism)
  • Point Mutation
  • Polycystic Ovary Syndrome (diagnosis, genetics)
  • RNA Precursors (metabolism)
  • RNA, Messenger (metabolism)
  • RNA, Transfer (genetics)
  • Sequence Alignment
  • Sequence Analysis, DNA

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