Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome

American Journal of Human Genetics

Volumn 62, Issue 6, 1998, Pages 1493-1499

  Naumova, A K ^a,e   Leppert, M ^b   Barker, D F ^c   Morgan, K ^d   Sapienza, C ^a  

^a TEMPLE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF UTAH   (United States)

^d MONTREAL GENERAL HOSPITAL   (Canada)

^e UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; EXTRACHROMOSOMAL INHERITANCE; FEMALE; GENE LOCUS; GENE MAPPING; GENETIC HETEROGENEITY; GENOME IMPRINTING; HUMAN; HUMAN CELL; INHERITANCE; MALE; NORMAL HUMAN; PRIORITY JOURNAL; RECOMBINANT GENE; SEX DIFFERENCE; X CHROMOSOME LINKAGE;

EID: 0031748497     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/301860     Document Type: Article

References (26)

1. Barker DF, Detz-Band JN, Donaldson CW, Andersen WL, Turco A, Pole AR, Willard HF, et al (1989) Further isolation characterization and physical localization of X chromosome RFLP markers, comparing VNTR-directed and random isolation strategies. Cytogenet Cell Genet 51:958
2. Biddle FG (1987) Segregation distortion of X-linked marker genes in interspecific crosses between Mus musculus and Mus spretus. Genome 29:389-392
3. Boyd Y (1996) Non-mendelian inheritance of X chromosome markers in interspecific backcrosses. Nat Genet 13:393-394
4. Cattanach BM, Raspberry C (1991) Identification of the Mus spretus Xce allele. Mouse Genome 89:565-566
5. Chakraborty R, Stivers DN, Deka R, Yu LM, Shriver MD, Ferrell RE (1996) Segregation distortion of the CTG repeats at the myotonic dystrophy locus. Am J Hum Genet 59: 109-118
6. Disteche CM (1995) Escape from X-inactivation in the human and mouse. Trends Genet 11:17-22
7. European Working Group on Cystic Fibrosis Genetics (1995) No evidence for segregation distortion of cystic fibrosis alleles among sibs of cystic fibrosis patients. Eur J Hum Genet 3:324-325
8. Evans K, Fryer A, Inglehearn C, Duvall-Young J, Wittaker JL, Gregory CY, Butler R, et al (1994) Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion. Nat Genet 6:210-213
9. Fain PR, Kort EN, Chance PF, Nguyen K, Redd DF, Econs MJ, Barker DF (1995) A 2D crossover-based map of the human X chromosome as a model for map integration. Nat Genet 9:261-266
10. Guo SW, Thompson EA (1989) Analysis of sparse contingency tables: Monte Carlo estimation of exact P-values. Tech rep 187. Department of Statistics, University of Washington, Seattle
11. _ (1992) Performing the exact test of Hardy-Weinberg proportion for multiple alleles. Biometrics 48:361-372
12. Herman GE, Blair HJ, Boyd Y, Brown SDM, de Gouyon B, Haynes A, Quaderi N (1996) Mouse X chromosome. Mamm Genome 6 Spec Issue 1:S317-S330
13. Jones MH, Furlong RA, Burkin H, Chalmers J, Brown GM, Khwaja O, Affara NA (1996) The Drosophila developmental gene fat facets has a human homologue in Xp11.4 which escapes X-inactivation and has related sequences on Yq11.2. Hum Mol Genet 5:1695-1701
14. Laird CD (1987) Proposed mechanism of inheritance and expression of the human fragile-X syndrome of mental retardation. Genetics 117:587-599
15. McKusick VA (1994) Mendelian inheritance in man: a catalog of human genes and genetic disorders, 11th ed. John Hopkins University Press, Baltimore and London
16. Miller AP, Gustashaw K, Wolff DJ, Rider SH, Monaco AP, Eble B, Schlessinger D, et al (1995) Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map Xp11.21-p11.22. Hum Mol Genet 4:731-739
17. Montagutelli X, Turner R, Nadeau JH (1996) Epistatic control of non-mendelian inheritance in mouse interspecific crosses. Genetics 143:1739-1752
18. Munier F, Spence MA, Pescia G, Balmer A, Gailloud C, Thonney F, Melle G, et al (1992) Paternal selection favoring mutant alleles of the retinoblastoma susceptibility gene. Hum Genet 89:508-512
19. Naumova AK, Olien L, Bird LM, Slamka C, Fonseca M, Verner A, Wang M, et al (1995) Transmission-ratio distortion of X chromosomes among the male offspring of females with skewed X-inactivation. Dev Genet 17:198-205
20. Naumova AK, Plenge RM, Bird, LM, Leppert, M, Morgan, K, Willard HF, Sapienza C (1996) Heritability of X chromosome-inactivation phenotype in a large family. Am J Hum Genet 58:1111-1119
21. Naumova AK, Sapienza C (1994) Genetics of retinoblastoma, revisited. Am J Hum Genet 54:264-273
22. Rubinsztein DC, Leggo J (1997) Non-mendelian transmission at the Machado-Joseph disease locus in normal females: preferential transmission of alleles with smaller CAG repeats. J Med Genet 34:234-236
23. Skuse DH, James RS, Bishop DVM, Coppins B, Dalton P, Aamodt-Leeper G, Bacarese-Hamilton M, et al (1997) Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature 387:705-708
24. Van den Hurk JA, Hendriks W, van de Pol DJ, Oerlemans F, Jaissle G, Ruther K, Kohler K, et al (1997) Mouse choroideremia gene mutation causes photoreceptor cell degeneration and is not transmitted trough the female germline. Hum Mol Genet 6:851-858
25. Zechner U, Reule M, Burgoyne PS, Schubert A, Orth A, Hameister H, Fundele R (1997) Paternal transmission of X-linked placental dysplasia in mouse interspecific hybrids. Genetics 146:1399-1405
26. Zechner U, Reule M, Orth A, Bonhomme F, Srack B (1996) An X-chromosome linked locus contributes to abnormal placental development in mouse interspecific hybrids. Nat Genet 12:398-403