Literature DB >> 15181541

A prevalent POLG CAG microsatellite length allele in humans and African great apes.

Anja T Rovio1, Josef Abel, Arja L Ahola, Aida M Andres, Jaume Bertranpetit, Antoine Blancher, Ronald E Bontrop, Leona G Chemnick, Howard J Cooke, James M Cummins, Heidi A Davis, David J Elliott, Ellen Fritsche, Timothy B Hargreave, Susan M G Hoffman, Anne M Jequier, Shu-Huei Kao, Heui-Soo Kim, David R Marchington, Denise Mehmet, Nel Otting, Joanna Poulton, Oliver A Ryder, Hans-Christian Schuppe, Osamu Takenaka, Yau-Huei Wei, Lars Wichmann, Howard T Jacobs.   

Abstract

The human nuclear gene for the catalytic subunit of mitochondrial DNA polymerase gamma ( POLG) contains within its coding region a CAG microsatellite encoding a polyglutamine repeat. Previous studies demonstrated an association between length variation at this repeat and male infertility, suggesting a mechanism whereby the prevalent (CAG)(10) allele, which occurs at a frequency of >80% in different populations, could be maintained by selection. Sequence analysis of the POLG CAG microsatellite region of more than 1000 human chromosomes reveals that virtually all allelic variation at the locus is accounted for by length variation of the CAG repeat. Analysis of POLG from African great apes shows that a prevalent length allele is present in each species, although its exact length is species-specific. In common chimpanzee ( Pan troglodytes) a number of different sequence variants contribute to the prevalent length allele, strongly supporting the idea that the length of the POLG microsatellite region, rather than its exact nucleotide or amino acid sequence, is what is maintained. Analysis of POLG in other primates indicates that the repeat has expanded from a shorter, glutamine-rich sequence, present in the common ancestor of Old and New World monkeys.

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Year:  2004        PMID: 15181541     DOI: 10.1007/s00335-004-3049-x

Source DB:  PubMed          Journal:  Mamm Genome        ISSN: 0938-8990            Impact factor:   2.957


  40 in total

1.  Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions.

Authors:  G Van Goethem; B Dermaut; A Löfgren; J J Martin; C Van Broeckhoven
Journal:  Nat Genet       Date:  2001-07       Impact factor: 38.330

2.  Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat.

Authors:  B Brinkmann; M Klintschar; F Neuhuber; J Hühne; B Rolf
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

3.  Concerted evolution of the tandemly repeated genes encoding primate U2 small nuclear RNA (the RNU2 locus) does not prevent rapid diversification of the (CT)n.(GA)n microsatellite embedded within the U2 repeat unit.

Authors:  D Liao; A M Weiner
Journal:  Genomics       Date:  1995-12-10       Impact factor: 5.736

4.  CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphisms.

Authors:  S Choudhry; M Mukerji; A K Srivastava; S Jain; S K Brahmachari
Journal:  Hum Mol Genet       Date:  2001-10-01       Impact factor: 6.150

5.  The comparative genomics of polyglutamine repeats: extreme differences in the codon organization of repeat-encoding regions between mammals and Drosophila.

Authors:  M M Albà; M F Santibáñez-Koref; J M Hancock
Journal:  J Mol Evol       Date:  2001-03       Impact factor: 2.395

6.  Genetic diversity of Y-specific STRs in chimpanzees (Pan troglodytes).

Authors:  L Gusmão; A González-Neira; C Alves; P Sánchez-Diz; E M Dauber; A Amorim; A Carracedo
Journal:  Am J Primatol       Date:  2002-05       Impact factor: 2.371

7.  Equilibrium distributions of microsatellite repeat length resulting from a balance between slippage events and point mutations.

Authors:  S Kruglyak; R T Durrett; M D Schug; C F Aquadro
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-01       Impact factor: 11.205

8.  The gamma subfamily of DNA polymerases: cloning of a developmentally regulated cDNA encoding Xenopus laevis mitochondrial DNA polymerase gamma.

Authors:  F Ye; J A Carrodeguas; D F Bogenhagen
Journal:  Nucleic Acids Res       Date:  1996-04-15       Impact factor: 16.971

9.  Microsatellite evolution inferred from human-chimpanzee genomic sequence alignments.

Authors:  Matthew T Webster; Nick G C Smith; Hans Ellegren
Journal:  Proc Natl Acad Sci U S A       Date:  2002-06-17       Impact factor: 11.205

10.  Length polymorphism of a microsatellite in human and non human primates.

Authors:  P Calvas; A Blancher; I Salvignol; W W Socha; J Ruffié
Journal:  C R Acad Sci III       Date:  1994-08
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  6 in total

1.  POLG1 polyglutamine tract variants associated with Parkinson's disease.

Authors:  Johanna Eerola; Petri T Luoma; Terhi Peuralinna; Sonja Scholz; Coro Paisan-Ruiz; Anu Suomalainen; Andrew B Singleton; Pentti J Tienari
Journal:  Neurosci Lett       Date:  2010-04-24       Impact factor: 3.046

2.  CAG-repeat variant in the polymerase γ gene and male infertility in the Chinese population: a meta-analysis.

Authors:  Shu-Yuan Liu; Chang-Jun Zhang; Hai-Ying Peng; Yu-Feng Yao; Lei Shi; Jin-Bao Chen; Ke-Qin Lin; Liang Yu; Li Shi; Xiao-Qin Huang; Hao Sun; Jia-You Chu
Journal:  Asian J Androl       Date:  2010-11-22       Impact factor: 3.285

3.  Mitochondrial DNA polymerase gamma gene polymorphism is not associated with male infertility.

Authors:  J Poongothai
Journal:  J Assist Reprod Genet       Date:  2013-08-04       Impact factor: 3.412

Review 4.  DNA polymerase gamma and mitochondrial disease: understanding the consequence of POLG mutations.

Authors:  Sherine S L Chan; William C Copeland
Journal:  Biochim Biophys Acta       Date:  2008-10-29

5.  CAG-encoded polyglutamine length polymorphism in the human genome.

Authors:  Stefanie L Butland; Rebecca S Devon; Yong Huang; Carri-Lyn Mead; Alison M Meynert; Scott J Neal; Soo Sen Lee; Anna Wilkinson; George S Yang; Macaire M S Yuen; Michael R Hayden; Robert A Holt; Blair R Leavitt; B F Francis Ouellette
Journal:  BMC Genomics       Date:  2007-05-22       Impact factor: 3.969

6.  The POLG Polyglutamine Tract Variants in Iranian Patients with Multiple Sclerosis.

Authors:  Mehri Khatami; Mohammad Mehdi Heidari; Reza Mansouri; Fatemeh Mousavi
Journal:  Iran J Child Neurol       Date:  2015
  6 in total

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