Literature DB >> 10968778

Hypervariable sites in the mtDNA control region are mutational hotspots.

M Stoneking1.   

Abstract

Hypervariable sites in human mtDNA are readily identified in evolutionary studies and are usually assumed to represent mutational hotspots. Recently, an alternative hypothesis was proposed that holds that hypervariable sites may instead reflect ancient mtDNA mutations that have been "shuffled" among different lineages via recombination. These hypotheses can be tested by examining the evolutionary rates for sites at which new mtDNA mutations are observed; if hypervariable sites are mutational hotspots, then newly arisen mtDNA mutations should occur preferentially at hypervariable sites. Results of this study show that both germline and somatic mtDNA mutations occur preferentially at hypervariable sites, which supports the view that hypervariable sites are indeed mutational hotspots.

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Year:  2000        PMID: 10968778      PMCID: PMC1287875          DOI: 10.1086/303092

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  24 in total

1.  Pattern of nucleotide substitution and rate heterogeneity in the hypervariable regions I and II of human mtDNA.

Authors:  S Meyer; G Weiss; A von Haeseler
Journal:  Genetics       Date:  1999-07       Impact factor: 4.562

2.  The mutation rate in the human mtDNA control region.

Authors:  S Sigurğardóttir; A Helgason; J R Gulcher; K Stefansson; P Donnelly
Journal:  Am J Hum Genet       Date:  2000-04-07       Impact factor: 11.025

3.  A sensitive denaturing gradient-Gel electrophoresis assay reveals a high frequency of heteroplasmy in hypervariable region 1 of the human mtDNA control region.

Authors:  L A Tully; T J Parsons; R J Steighner; M M Holland; M A Marino; V L Prenger
Journal:  Am J Hum Genet       Date:  2000-06-28       Impact factor: 11.025

4.  Questioning evidence for recombination in human mitochondrial DNA.

Authors:  T Kivisild; R Villems
Journal:  Science       Date:  2000-06-16       Impact factor: 47.728

5.  Evidence for mitochondrial DNA recombination in a human population of island Melanesia.

Authors:  E Hagelberg; N Goldman; P Lió; S Whelan; W Schiefenhövel; J B Clegg; D K Bowden
Journal:  Proc Biol Sci       Date:  1999-03-07       Impact factor: 5.349

6.  Substitution rate variation among sites in hypervariable region 1 of human mitochondrial DNA.

Authors:  J Wakeley
Journal:  J Mol Evol       Date:  1993-12       Impact factor: 2.395

7.  Sequence and organization of the human mitochondrial genome.

Authors:  S Anderson; A T Bankier; B G Barrell; M H de Bruijn; A R Coulson; J Drouin; I C Eperon; D P Nierlich; B A Roe; F Sanger; P H Schreier; A J Smith; R Staden; I G Young
Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

8.  How clonal are human mitochondria?

Authors:  A Eyre-Walker; N H Smith; J M Smith
Journal:  Proc Biol Sci       Date:  1999-03-07       Impact factor: 5.349

9.  Heteroplasmic point mutations in the human mtDNA control region.

Authors:  K E Bendall; V A Macaulay; J R Baker; B C Sykes
Journal:  Am J Hum Genet       Date:  1996-12       Impact factor: 11.025

10.  Toward a more accurate time scale for the human mitochondrial DNA tree.

Authors:  M Hasegawa; A Di Rienzo; T D Kocher; A C Wilson
Journal:  J Mol Evol       Date:  1993-10       Impact factor: 2.395

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  77 in total

1.  Analysis of European mtDNAs for recombination.

Authors:  J L Elson; R M Andrews; P F Chinnery; R N Lightowlers; D M Turnbull; N Howell
Journal:  Am J Hum Genet       Date:  2000-12-11       Impact factor: 11.025

2.  Origins and divergence of the Roma (gypsies).

Authors:  D Gresham; B Morar; P A Underhill; G Passarino; A A Lin; C Wise; D Angelicheva; F Calafell; P J Oefner; P Shen; I Tournev; R de Pablo; V Kuĉinskas; A Perez-Lezaun; E Marushiakova; V Popov; L Kalaydjieva
Journal:  Am J Hum Genet       Date:  2001-11-09       Impact factor: 11.025

3.  The structure of diversity within New World mitochondrial DNA haplogroups: implications for the prehistory of North America.

Authors:  Ripan S Malhi; Jason A Eshleman; Jonathan A Greenberg; Deborah A Weiss; Beth A Schultz Shook; Frederika A Kaestle; Joseph G Lorenz; Brian M Kemp; John R Johnson; David Glenn Smith
Journal:  Am J Hum Genet       Date:  2002-02-13       Impact factor: 11.025

4.  Phylogenetic and familial estimates of mitochondrial substitution rates: study of control region mutations in deep-rooting pedigrees.

Authors:  E Heyer; E Zietkiewicz; A Rochowski; V Yotova; J Puymirat; D Labuda
Journal:  Am J Hum Genet       Date:  2001-10-01       Impact factor: 11.025

5.  Distribution patterns of postmortem damage in human mitochondrial DNA.

Authors:  M Thomas P Gilbert; Eske Willerslev; Anders J Hansen; Ian Barnes; Lars Rudbeck; Niels Lynnerup; Alan Cooper
Journal:  Am J Hum Genet       Date:  2002-12-12       Impact factor: 11.025

6.  Twinkle and POLG defects enhance age-dependent accumulation of mutations in the control region of mtDNA.

Authors:  Sjoerd Wanrooij; Petri Luoma; Gert van Goethem; Christine van Broeckhoven; Anu Suomalainen; Johannes N Spelbrink
Journal:  Nucleic Acids Res       Date:  2004-06-04       Impact factor: 16.971

7.  Evidence that the large noncoding sequence is the main control region of maternally and paternally transmitted mitochondrial genomes of the marine mussel (Mytilus spp.).

Authors:  Liqin Cao; Ellen Kenchington; Eleftherios Zouros; George C Rodakis
Journal:  Genetics       Date:  2004-06       Impact factor: 4.562

Review 8.  Variation in the mutation rate across mammalian genomes.

Authors:  Alan Hodgkinson; Adam Eyre-Walker
Journal:  Nat Rev Genet       Date:  2011-10-04       Impact factor: 53.242

9.  Different characteristics of mitochondrial microsatellite instability between uterine leiomyomas and leiomyosarcomas.

Authors:  Jae-Ho Lee; Tae-Yung Ryu; Chi-Heum Cho; Dae-Kwang Kim
Journal:  Pathol Oncol Res       Date:  2010-09-18       Impact factor: 3.201

10.  Identification of sequence polymorphisms in the mitochondrial displacement loop as risk factors for sporadic and familial breast cancer.

Authors:  Meng Cheng; Zhanjun Guo; Haiping Li; Zheng Li; Chunxiao Li; Cuizhi Geng
Journal:  Tumour Biol       Date:  2014-01-16
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