Differences of sperm motility in mitochondrial DNA haplogroup U sublineages

Gene

Volumn 368, Issue 1-2, 2006, Pages 21-27

  Montiel Sosa, Francisco ^a,b   Ruiz Pesini, Eduardo ^a,c   Enríquez, José Antonio ^a   Marcuello, Ana ^a   Díez Sánchez, Carmen ^a   Montoya, Julio ^a   Wallace, Douglas C ^c   López Pérez, Manuel José ^a  

^a UNIVERSITY OF ZARAGOZA   (Spain)

^b UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Haplogroup; Mitochondrial DNA; OXPHOS; Phylogeography; Sperm motility

Indexed keywords

CYTOCHROME B; MITOCHONDRIAL RNA;

ADULT; ARTICLE; CELL FUNCTION; COLD ACCLIMATIZATION; CORRELATION FUNCTION; CRYSTAL STRUCTURE; ENERGY METABOLISM; EUROPE; GENE IDENTIFICATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; HAPLOTYPE; HUMAN; HUMAN CELL; MALE; MISSENSE MUTATION; MITOCHONDRIAL RESPIRATION; OXIDATIVE PHOSPHORYLATION; PHYLOGEOGRAPHY; PRIORITY JOURNAL; SEMEN ANALYSIS; SOUTHERN EUROPE; SPERMATOZOON MOTILITY;

ADULT; CELL LINEAGE; CONSENSUS SEQUENCE; CYTOCHROMES B; DATA INTERPRETATION, STATISTICAL; DNA, MITOCHONDRIAL; EVOLUTION, MOLECULAR; HAPLOTYPES; HUMANS; MALE; MUTATION, MISSENSE; SPERM MOTILITY;

EID: 33344470193     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.gene.2005.09.015     Document Type: Article

References (35)

1. A. Achilli Saami and berbers-an unexpected mitochondrial DNA link Am. J. Hum. Genet. 76 2005 883 886
2. M. Bonafe An allele of HRAS1 3′ variable number of tandem repeats is a frailty allele: implication for an evolutionarily-conserved pathway involved in longevity Gene 286 2002 121 126
3. M.D. Brown, F. Sun, and D.C. Wallace Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage Am. J. Hum. Genet. 60 1997 381 387
4. G. Carrieri Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease Hum. Genet. 108 2001 194 198
5. P.E. Coskun, E. Ruiz-Pesini, and D.C. Wallace Control region mtDNA variants: longevity, climatic adaptation, and a forensic conundrum Proc. Natl. Acad. Sci. U. S. A. 100 2003 2174 2176
6. A.R. Crofts Mechanism of ubiquinol oxidation by the bc(1) complex: role of the iron sulfur protein and its mobility Biochemistry 38 1999 15791 15806
7. G. De Benedictis Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans FASEB J. 13 1999 1532 1536
8. J.P. di Rago, and A.M. Colson Molecular basis for resistance to antimycin and diuron, Q-cycle inhibitors acting at the Qi site in the mitochondrial ubiquinol-cytochrome c reductase in Saccharomyces cerevisiae J. Biol. Chem. 263 1988 12564 12570
9. J.L. Elson, D.M. Turnbull, and N. Howell Comparative genomics and the evolution of human mitochondrial DNA: assessing the effects of selection Am. J. Hum. Genet. 74 2004 229 238
10. N. Fisher, and P.R. Rich A motif for quinone binding sites in respiratory and photosynthetic systems J. Mol. Biol. 296 2000 1153 1162
11. C. Florentz, and M. Sissler Disease-related versus polymorphic mutations in human mitochondrial tRNAs. Where is the difference? EMBO Rep. 2 2001 481 486
12. D. Ghezzi Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians Eur. J. Hum. Genet. 13 6 2005 748 752 (Jun)
13. J.P. Hosler The influence of subunit III of cytochrome c oxidase on the D pathway, the proton exit pathway and mechanism-based inactivation in subunit I Biochim. Biophys. Acta 1655 2004 332 339
14. R. Ivanova, V. Lepage, D. Charron, and F. Schachter Mitochondrial genotype associated with French Caucasian centenarians Gerontology 44 1998 349
15. S. Kumar, K. Tamura, I.B. Jakobsen, and M. Nei MEGA2: molecular evolutionary genetics analysis software Bioinformatics 17 2001 1244 1245
16. B.A. Malyarchuk Differentiation of the mitochondrial subhaplogroup U4 in the populations of Eastern Europe, Ural, and Western Siberia: implication to the genetic history of the Uralic populations Genetika 40 2004 1549 1556
17. M.W. Mather, and H. Rottenberg Intrinsic uncoupling of cytochrome c oxidase may cause the maternally inherited mitochondrial diseases MELAS and LHON FEBS Lett. 433 1998 93 97
18. B. Meunier, and J.W. Taanman Mutations of cytochrome c oxidase subunits 1 and 3 in Saccharomyces cerevisiae: assembly defect and compensation Biochim. Biophys. Acta 1554 2002 101 107
19. D. Mishmar Natural selection shaped regional mtDNA variation in humans Proc. Natl. Acad. Sci. U. S. A. 100 2003 171 176
20. A.K. Niemi, A. Hervonen, M. Hurme, P.J. Karhunen, M. Jylha, and K. Majamaa Mitochondrial DNA polymorphisms associated with longevity in a Finnish population Hum. Genet. 112 2003 29 33
21. A. Pyle Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD Ann. Neurol. 57 2005 564 567
22. O.A. Ross Mitochondrial DNA polymorphism: its role in longevity of the Irish population Exp. Gerontol. 36 2001 1161 1178
23. E. Ruiz-Pesini Correlation of sperm motility with mitochondrial enzymatic activities Clin. Chem. 44 1998 1616 1620
24. E. Ruiz-Pesini Human mtDNA haplogroups associated with high or reduced spermatozoa motility Am. J. Hum. Genet. 67 2000 682 696
25. E. Ruiz-Pesini, D. Mishmar, M. Brandon, V. Procaccio, and D.C. Wallace Effects of purifying and adaptive selection on regional variation in human mtDNA Science 303 2004 223 226
26. S. Solakidi, and C.E. Sekeris Oligonucleotide sequences similar to transcription factor consensi of nuclear genes are present in the human mitochondrial genome Anticancer Res. 23 2003 1389 1393
27. A. Torroni Classification of European mtDNAs from an analysis of three European populations Genetics 144 1996 1835 1850
28. A. Torroni Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484 Am. J. Hum. Genet. 60 1997 1107 1121
29. L. Troiano Mitochondrial membrane potential and DNA stainability in human sperm cells: a flow cytometry analysis with implications for male infertility Exp. Cell Res. 241 1998 384 393
30. J.M. van der Walt Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease Am. J. Hum. Genet. 72 2003 804 811
31. J.M. van der Walt Analysis of European mitochondrial haplogroups with Alzheimer disease risk Neurosci. Lett. 365 2004 28 32
32. D.C. Wallace Mitochondrial DNA mutations in diseases of energy metabolism J. Bioenerg. Biomembranes 26 1994 241 250
33. D.C. Wallace, M.D. Brown, and M.T. Lott Mitochondrial DNA variation in human evolution and disease Gene 238 1999 211 230
34. D.C. Wallace, E. Ruiz-Pesini, and D. Mishmar mtDNA variation, climatic adaptation, degenerative diseases, and longevity Cold Spring Harbor Symp. Quant. Biol. 68 2003 479 486
35. WHO WHO Laboratory Manual for the Examination of Human Semen and Semen-Cervical Mucus Interaction 1992 Cambridge University Press Cambridge