Literature DB >> 7683672

Post-transcriptional regulation of the steady-state levels of mitochondrial tRNAs in HeLa cells.

M P King1, G Attardi.   

Abstract

In human mitochondrial DNA (mtDNA), the tRNA genes are located in three different transcription units that are transcribed at three different rates. To analyze the regulation of tRNA formation by the three transcription units, we have examined the steady-state levels and metabolic properties of the tRNAs of HeLa cell mitochondria. DNA excess hybridization experiments utilizing separated strands of mtDNA and purified tRNA samples from exponential cells long term labeled with [32P]orthophosphate have revealed a steady-state level of 6 x 10(5) tRNA molecules/cell, with three-fourths being encoded in the H-strand and one-fourth in the L-strand. Hybridization of the tRNAs with a panel of M13 clones of human mtDNA containing, in most cases, single tRNA genes and a quantitation of two-dimensional electrophoretic fractionations of the tRNAs have shown that the steady-state levels of tRNA(Phe) and tRNA(Val) are two to three times higher than the average level of the other H-strand-encoded tRNAs and three to four times higher than the average level of the L-strand-encoded tRNAs. Similar experiments carried out with tRNAs isolated from cells labeled with very short pulses of [5-3H]uridine have indicated that the rates of formation of the individual tRNA species are proportional to their steady-state amounts. Therefore, the approximately 25-fold higher rate of transcription of the tRNA(Phe) and tRNA(Val) genes relative to the other H-strand tRNA genes and the 10-16-fold higher rate of transcription of the L-strand tRNA genes relative to the H-strand tRNA genes are not reflected in the steady-state levels or the rates of formation of the corresponding tRNAs. A comparison of the steady-state levels of the individual tRNAs with the corresponding codon usage for protein synthesis, as determined from the DNA sequence and the rates of synthesis of the various polypeptides, has not revealed any significant correlation between the two parameters.

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Year:  1993        PMID: 7683672

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  51 in total

1.  The RNase P associated with HeLa cell mitochondria contains an essential RNA component identical in sequence to that of the nuclear RNase P.

Authors:  R S Puranam; G Attardi
Journal:  Mol Cell Biol       Date:  2001-01       Impact factor: 4.272

2.  Difference between mitochondrial RNase P and nuclear RNase P.

Authors:  W Rossmanith; T Potuschak
Journal:  Mol Cell Biol       Date:  2001-12       Impact factor: 4.272

Review 3.  Mitochondrial genetic control of assembly and function of complex I in mammalian cells.

Authors:  A Chomyn
Journal:  J Bioenerg Biomembr       Date:  2001-06       Impact factor: 2.945

4.  Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations.

Authors:  Min-Xin Guan; Qingfeng Yan; Xiaoming Li; Yelena Bykhovskaya; Jaime Gallo-Teran; Petr Hajek; Noriko Umeda; Hui Zhao; Gema Garrido; Emebet Mengesha; Tsutomu Suzuki; Ignacio del Castillo; Jennifer Lynne Peters; Ronghua Li; Yaping Qian; Xinjian Wang; Ester Ballana; Mordechai Shohat; Jianxin Lu; Xavier Estivill; Kimitsuna Watanabe; Nathan Fischel-Ghodsian
Journal:  Am J Hum Genet       Date:  2006-06-22       Impact factor: 11.025

5.  Coronary heart disease is associated with a mutation in mitochondrial tRNA.

Authors:  Zidong Jia; Xinjian Wang; Yanwen Qin; Ling Xue; Pingping Jiang; Yanzi Meng; Suxue Shi; Yan Wang; Jun Qin Mo; Min-Xin Guan
Journal:  Hum Mol Genet       Date:  2013-06-04       Impact factor: 6.150

6.  Biochemical Evidence for a Nuclear Modifier Allele (A10S) in TRMU (Methylaminomethyl-2-thiouridylate-methyltransferase) Related to Mitochondrial tRNA Modification in the Phenotypic Manifestation of Deafness-associated 12S rRNA Mutation.

Authors:  Feilong Meng; Xiaohui Cang; Yanyan Peng; Ronghua Li; Zhengyue Zhang; Fushan Li; Qingqing Fan; Anna S Guan; Nathan Fischel-Ghosian; Xiaoli Zhao; Min-Xin Guan
Journal:  J Biol Chem       Date:  2017-01-03       Impact factor: 5.157

7.  Evidence for aminoacylation-induced conformational changes in human mitochondrial tRNAs.

Authors:  J A Enríquez; G Attardi
Journal:  Proc Natl Acad Sci U S A       Date:  1996-08-06       Impact factor: 11.205

8.  Naturally occurring dual recognition of tRNAHis substrates with and without a universal identity element.

Authors:  Yi-Hsueh Lee; Ya-Ting Lo; Chia-Pei Chang; Chung-Shu Yeh; Tien-Hsien Chang; Yu-Wei Chen; Yi-Kuan Tseng; Chien-Chia Wang
Journal:  RNA Biol       Date:  2019-06-16       Impact factor: 4.652

9.  Evidence for the presence of 5S rRNA in mammalian mitochondria.

Authors:  P J Magalhães; A L Andreu; E A Schon
Journal:  Mol Biol Cell       Date:  1998-09       Impact factor: 4.138

10.  Gene expression patterns of oxidative phosphorylation complex I subunits are organized in clusters.

Authors:  Yael Garbian; Ofer Ovadia; Sarah Dadon; Dan Mishmar
Journal:  PLoS One       Date:  2010-04-01       Impact factor: 3.240

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