Literature DB >> 8808591

The mutation rate of the human mtDNA deletion mtDNA4977.

R Shenkar1, W Navidi, S Tavaré, M H Dang, A Chomyn, G Attardi, G Cortopassi, N Arnheim.   

Abstract

The human mitochondrial mutation mtDNA4977 is a 4,977-bp deletion that originates between two 13-bp direct repeats. We grew 220 colonies of cells, each from a single human cell. For each colony, we counted the number of cells and amplified the DNA by PCR to test for the presence of a deletion. To estimate the mutation fate, we used a model that describes the relationship between the mutation rate and the probability that a colony of a given size will contain no mutants, taking into account such factors as possible mitochondrial turnover and mistyping due to PCR error. We estimate that the mutation rate for mtDNA4977 in cultured human cells is 5.95 x 10(-8) per mitochondrial genome replication. This method can be applied to specific chromosomal, as well as mitochondrial, mutations.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 8808591      PMCID: PMC1914802     

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


  13 in total

1.  Detection of a specific mitochondrial DNA deletion in tissues of older humans.

Authors:  G A Cortopassi; N Arnheim
Journal:  Nucleic Acids Res       Date:  1990-12-11       Impact factor: 16.971

2.  Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy.

Authors:  M Yoneda; A Chomyn; A Martinuzzi; O Hurko; G Attardi
Journal:  Proc Natl Acad Sci U S A       Date:  1992-12-01       Impact factor: 11.205

3.  Multiple mitochondrial DNA deletions in an elderly human individual.

Authors:  C Zhang; A Baumer; R J Maxwell; A W Linnane; P Nagley
Journal:  FEBS Lett       Date:  1992-02-03       Impact factor: 4.124

4.  Mutations of Bacteria from Virus Sensitivity to Virus Resistance.

Authors:  S E Luria; M Delbrück
Journal:  Genetics       Date:  1943-11       Impact factor: 4.562

5.  Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain.

Authors:  N W Soong; D R Hinton; G Cortopassi; N Arnheim
Journal:  Nat Genet       Date:  1992-12       Impact factor: 38.330

Review 6.  Pitfalls and practice of Luria-Delbrück fluctuation analysis: a review.

Authors:  W S Kendal; P Frost
Journal:  Cancer Res       Date:  1988-03-01       Impact factor: 12.701

7.  5-bromodeoxyuridine labeling of monomeric and catenated circular mitochondrial DNA in HeLa cells.

Authors:  P J Flory; J Vinograd
Journal:  J Mol Biol       Date:  1973-02-25       Impact factor: 5.469

8.  Ageing-associated 5 kb deletion in human liver mitochondrial DNA.

Authors:  T C Yen; J H Su; K L King; Y H Wei
Journal:  Biochem Biophys Res Commun       Date:  1991-07-15       Impact factor: 3.575

Review 9.  Mitochondrial DNA sequence variation in human evolution and disease.

Authors:  D C Wallace
Journal:  Proc Natl Acad Sci U S A       Date:  1994-09-13       Impact factor: 11.205

10.  Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac disease.

Authors:  M Corral-Debrinski; G Stepien; J M Shoffner; M T Lott; K Kanter; D C Wallace
Journal:  JAMA       Date:  1991-10-02       Impact factor: 56.272

View more
  14 in total

1.  Mutational analysis of the human mitochondrial genome branches into the realm of bacterial genetics.

Authors:  N Howell
Journal:  Am J Hum Genet       Date:  1996-10       Impact factor: 11.025

2.  Molecular Population Genetics of the Northern Elephant Seal Mirounga angustirostris.

Authors:  Alicia Abadía-Cardoso; Nelson B Freimer; Kristy Deiner; John Carlos Garza
Journal:  J Hered       Date:  2017-09-01       Impact factor: 2.645

Review 3.  Mitochondrial-nuclear epistasis: implications for human aging and longevity.

Authors:  Gregory J Tranah
Journal:  Ageing Res Rev       Date:  2010-06-25       Impact factor: 10.895

4.  Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age.

Authors:  J L Elson; D C Samuels; D M Turnbull; P F Chinnery
Journal:  Am J Hum Genet       Date:  2001-02-06       Impact factor: 11.025

Review 5.  Somatic mosaicism: implications for disease and transmission genetics.

Authors:  Ian M Campbell; Chad A Shaw; Pawel Stankiewicz; James R Lupski
Journal:  Trends Genet       Date:  2015-04-21       Impact factor: 11.639

6.  Analysis of mtDNA, miR-155 and BACH1 expression in hearts from donors with and without Down syndrome.

Authors:  Erik Hefti; Adolfo Quiñones-Lombraña; Almedina Redzematovic; Jeffrey Hui; Javier G Blanco
Journal:  Mitochondrial DNA A DNA Mapp Seq Anal       Date:  2014-06-18       Impact factor: 1.514

7.  Age-dependent deficiency in import of mitochondrial DNA glycosylases required for repair of oxidatively damaged bases.

Authors:  Bartosz Szczesny; Tapas K Hazra; John Papaconstantinou; Sankar Mitra; Istvan Boldogh
Journal:  Proc Natl Acad Sci U S A       Date:  2003-09-05       Impact factor: 11.205

8.  Mitochondria and familial predisposition to breast cancer.

Authors:  Stefania Weigl; Angelo Paradiso; Stefania Tommasi
Journal:  Curr Genomics       Date:  2013-05       Impact factor: 2.236

9.  Impairment of myocardial mitochondria in viral myocardial disease and its reflective window in peripheral cells.

Authors:  Jin Wei; Deng-Feng Gao; Hao Wang; Rui Yan; Zhi-Quan Liu; Zu-Yi Yuan; Jian Liu; Ming-Xia Chen
Journal:  PLoS One       Date:  2014-12-31       Impact factor: 3.240

10.  Mitochondrial common deletion, a potential biomarker for cancer occurrence, is selected against in cancer background: a meta-analysis of 38 studies.

Authors:  Hezhongrong Nie; Hongying Shu; Rasika Vartak; Amanda Claire Milstein; Yalin Mo; Xiaoqin Hu; Hezhi Fang; Lijun Shen; Zhinan Ding; Jianxin Lu; Yidong Bai
Journal:  PLoS One       Date:  2013-07-04       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.