Literature DB >> 15336535

The 7472insC mtDNA mutation impairs 5' and 3' processing of tRNA(Ser(UCN)).

Marina Toompuu1, Louis L Levinger, Anna Nadal, Jordi Gomez, Howard T Jacobs.   

Abstract

The deafness-associated 7472insC mtDNA mutation was previously shown to decrease the steady-state level of tRNA(Ser(UCN)) post-transcriptionally. To identify the affected tRNA maturation step(s) we analysed the effects of the mutation on processing in vivo and in vitro. tRNA(Ser(UCN)) from cybrid cells homoplasmic for 7472insC contained a high frequency (>11%) of molecules misprocessed at one or both termini. In vitro assays using partially purified HeLa cell RNase P and mitochondrial tRNA 3' processing endonuclease (tRNase Z) confirmed that the efficiency of both 5' and 3' processing was impaired. A mutant precursor not already processed at the 5' end was poorly processed in vitro by tRNase Z. Misprocessing at the 3' end further impaired the efficiency and accuracy of 5' processing of the mutant substrate. The mutation thus appears to affect several distinct, but interdependent, RNA processing steps, with the predicted outcome dependent on the exact processing pathway operating in vivo.

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Year:  2004        PMID: 15336535     DOI: 10.1016/j.bbrc.2004.07.181

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  7 in total

Review 1.  Mitochondrial tRNA 3' end metabolism and human disease.

Authors:  Louis Levinger; Mario Mörl; Catherine Florentz
Journal:  Nucleic Acids Res       Date:  2004-10-11       Impact factor: 16.971

2.  Pathogenesis-related mutations in the T-loops of human mitochondrial tRNAs affect 3' end processing and tRNA structure.

Authors:  Louis Levinger; Dmitri Serjanov
Journal:  RNA Biol       Date:  2012-03-01       Impact factor: 4.652

3.  Noncanonical secondary structure stabilizes mitochondrial tRNA(Ser(UCN)) by reducing the entropic cost of tertiary folding.

Authors:  Anthony M Mustoe; Xin Liu; Paul J Lin; Hashim M Al-Hashimi; Carol A Fierke; Charles L Brooks
Journal:  J Am Chem Soc       Date:  2015-03-09       Impact factor: 15.419

Review 4.  Molecular oncology focus - is carcinogenesis a 'mitochondriopathy'?

Authors:  Anna M Czarnecka; Jerzy S Czarnecki; Wojciech Kukwa; Francesco Cappello; Anna Scińska; Andrzej Kukwa
Journal:  J Biomed Sci       Date:  2010-04-25       Impact factor: 8.410

5.  A new mechanism for mtDNA pathogenesis: impairment of post-transcriptional maturation leads to severe depletion of mitochondrial tRNASer(UCN) caused by T7512C and G7497A point mutations.

Authors:  Myriam Möllers; Katharina Maniura-Weber; Emina Kiseljakovic; Maria Bust; Armine Hayrapetyan; Michaela Jaksch; Mark Helm; Rudolf J Wiesner; Jürgen-Christoph von Kleist-Retzow
Journal:  Nucleic Acids Res       Date:  2005-09-30       Impact factor: 16.971

6.  Polyadenylation and degradation of structurally abnormal mitochondrial tRNAs in human cells.

Authors:  Marina Toompuu; Tea Tuomela; Pia Laine; Lars Paulin; Eric Dufour; Howard T Jacobs
Journal:  Nucleic Acids Res       Date:  2018-06-01       Impact factor: 16.971

7.  Prevalence of mitochondrial DNA mutations in sporadic patients with nonsyndromic sensorineural hearing loss.

Authors:  Hua Jiang; Jia Chen; Ying Li; Peng-Fang Lin; Jian-Guo He; Bei-Bei Yang
Journal:  Braz J Otorhinolaryngol       Date:  2015-11-05
  7 in total

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