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. 2000 Jan;154(1):343–350. doi: 10.1093/genetics/154.1.343

Sex-of-offspring-specific transmission ratio distortion on mouse chromosome X.

E de la Casa-Esperon 1, F Pardo-Manuel de Villena 1, A E Verner 1, T L Briscoe 1, J M Malette 1, M Rosa 1, W H Jin 1, C Sapienza 1
PMCID: PMC1460928  PMID: 10628993

Abstract

During our study of the DDK syndrome, we observed sex ratio distortion in favor of males among the offspring of F(1) backcrosses between the C57BL/6 and DDK strains. We also observed significant and reproducible transmission ratio distortion in favor of the inheritance of DDK alleles at loci on chromosome X among female offspring but not among male offspring in (C57BL/6 x DDK)F(1) x C57BL/6 and (C57BL/6-Pgk1(a) x DDK)F(1) x C57BL/6 backcrosses. The observed transmission ratio distortion is maximum at DXMit210 in the central region of chromosome X and decreases progressively at proximal and distal loci, in a manner consistent with the predictions of a single distorted locus model. DXMit210 is closely linked to two distortion-controlling loci (Dcsx1 and Dcsx2) described previously in interspecific backcrosses. Our analysis suggests that the female-offspring-specific transmission ratio distortion we observe is likely to be the result of the death of embryos of particular genotypic combinations. In addition, we confirm the previous suggestion that the transmission ratio distortion observed on chromosome X in interspecific backcrosses is also the result of loss of embryos.

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Selected References

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  1. Babinet C., Richoux V., Guénet J. L., Renard J. P. The DDK inbred strain as a model for the study of interactions between parental genomes and egg cytoplasm in mouse preimplantation development. Dev Suppl. 1990:81–87. [PubMed] [Google Scholar]
  2. Biddle F. G. Segregation distortion of X-linked marker genes in interspecific crosses between Mus musculus and M. spretus. Genome. 1987 Apr;29(2):389–392. doi: 10.1139/g87-067. [DOI] [PubMed] [Google Scholar]
  3. Boyd Y. Non-mendelian inheritance of X chromosome markers in interspecific backcrosses. Nat Genet. 1996 Aug;13(4):393–394. doi: 10.1038/ng0896-393. [DOI] [PubMed] [Google Scholar]
  4. Gubbay J., Collignon J., Koopman P., Capel B., Economou A., Münsterberg A., Vivian N., Goodfellow P., Lovell-Badge R. A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes. Nature. 1990 Jul 19;346(6281):245–250. doi: 10.1038/346245a0. [DOI] [PubMed] [Google Scholar]
  5. Johnson K. R., Cook S. A., Davisson M. T. Identification and genetic mapping of 151 dispersed members of 16 ribosomal protein multigene families in the mouse. Mamm Genome. 1994 Nov;5(11):670–687. doi: 10.1007/BF00426073. [DOI] [PubMed] [Google Scholar]
  6. Naumova A. K., Leppert M., Barker D. F., Morgan K., Sapienza C. Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome. Am J Hum Genet. 1998 Jun;62(6):1493–1499. doi: 10.1086/301860. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Pardo-Manual de Villena F., Slamka C., Fonseca M., Naumova A. K., Paquette J., Pannunzio P., Smith M., Verner A., Morgan K., Sapienza C. Transmission-ratio distortion through F1 females at chromosome 11 loci linked to Om in the mouse DDK syndrome. Genetics. 1996 Apr;142(4):1299–1304. doi: 10.1093/genetics/142.4.1299. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Pardo-Manual de Villena F., Slamka C., Fonseca M., Naumova A. K., Paquette J., Pannunzio P., Smith M., Verner A., Morgan K., Sapienza C. Transmission-ratio distortion through F1 females at chromosome 11 loci linked to Om in the mouse DDK syndrome. Genetics. 1996 Apr;142(4):1299–1304. doi: 10.1093/genetics/142.4.1299. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Pardo-Manuel de Villena F., Naumova A. K., Verner A. E., Jin W. H., Sapienza C. Confirmation of maternal transmission ratio distortion at Om and direct evidence that the maternal and paternal "DDK syndrome" genes are linked. Mamm Genome. 1997 Sep;8(9):642–646. doi: 10.1007/s003359900529. [DOI] [PubMed] [Google Scholar]
  10. Pardo-Manuel de Villena F., Sapienza C. Genetic mapping of DXYMov15-associated sequences in the pseudoautosomal region of the C57BL/6J strain. Mamm Genome. 1996 Mar;7(3):237–239. doi: 10.1007/s003359900067. [DOI] [PubMed] [Google Scholar]
  11. Pardo-Manuel de Villena F., de la Casa-Esperon E., Briscoe T. L., Malette J. M., Sapienza C. Male-offspring-specific, haplotype-dependent, nonrandom cosegregation of alleles at loci on two mouse chromosomes. Genetics. 2000 Jan;154(1):351–356. doi: 10.1093/genetics/154.1.351. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Pardo-Manuel de Villena F., de la Casa-Esperon E., Briscoe T. L., Sapienza C. A genetic test to determine the origin of maternal transmission ratio distortion. Meiotic drive at the mouse Om locus. Genetics. 2000 Jan;154(1):333–342. doi: 10.1093/genetics/154.1.333. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Pardo-Manuel de Villena F., de la Casa-Esperón E., Verner A., Morgan K., Sapienza C. The maternal DDK syndrome phenotype is determined by modifier genes that are not linked to Om. Mamm Genome. 1999 May;10(5):492–497. doi: 10.1007/s003359901029. [DOI] [PubMed] [Google Scholar]
  14. Renard J. P., Babinet C. Identification of a paternal developmental effect on the cytoplasm of one-cell-stage mouse embryos. Proc Natl Acad Sci U S A. 1986 Sep;83(18):6883–6886. doi: 10.1073/pnas.83.18.6883. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Renard J. P., Baldacci P., Richoux-Duranthon V., Pournin S., Babinet C. A maternal factor affecting mouse blastocyst formation. Development. 1994 Apr;120(4):797–802. doi: 10.1242/dev.120.4.797. [DOI] [PubMed] [Google Scholar]
  16. Renard J. P., Baldacci P., Richoux-Duranthon V., Pournin S., Babinet C. A maternal factor affecting mouse blastocyst formation. Development. 1994 Apr;120(4):797–802. doi: 10.1242/dev.120.4.797. [DOI] [PubMed] [Google Scholar]
  17. Rowe L. B., Nadeau J. H., Turner R., Frankel W. N., Letts V. A., Eppig J. T., Ko M. S., Thurston S. J., Birkenmeier E. H. Maps from two interspecific backcross DNA panels available as a community genetic mapping resource. Mamm Genome. 1994 May;5(5):253–274. doi: 10.1007/BF00389540. [DOI] [PubMed] [Google Scholar]
  18. Sapienza C., Paquette J., Pannunzio P., Albrechtson S., Morgan K. The polar-lethal Ovum mutant gene maps to the distal portion of mouse chromosome 11. Genetics. 1992 Sep;132(1):241–246. doi: 10.1093/genetics/132.1.241. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Simmler M. C., Cattanach B. M., Rasberry C., Rougeulle C., Avner P. Mapping the murine Xce locus with (CA)n repeats. Mamm Genome. 1993 Sep;4(9):523–530. doi: 10.1007/BF00364788. [DOI] [PubMed] [Google Scholar]
  20. Wakasugi N. A genetically determined incompatibility system between spermatozoa and eggs leading to embryonic death in mice. J Reprod Fertil. 1974 Nov;41(1):85–96. doi: 10.1530/jrf.0.0410085. [DOI] [PubMed] [Google Scholar]
  21. Wakasugi N. Studies on fertility of DDK mice: reciprocal crosses between DDK and C57BL/6J strains and experimental transplantation of the ovary. J Reprod Fertil. 1973 May;33(2):283–291. doi: 10.1530/jrf.0.0330283. [DOI] [PubMed] [Google Scholar]
  22. Wakasugi N., Tomita T., Kondo K. Differences of fertility in reciprocal crosses between inbred strains of mice. DDK, KK and NC. J Reprod Fertil. 1967 Feb;13(1):41–50. doi: 10.1530/jrf.0.0130041. [DOI] [PubMed] [Google Scholar]
  23. Zechner U., Reule M., Burgoyne P. S., Schubert A., Orth A., Hameister H., Fundele R. Paternal transmission of X-linked placental dysplasia in mouse interspecific hybrids. Genetics. 1997 Aug;146(4):1399–1405. doi: 10.1093/genetics/146.4.1399. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Zechner U., Reule M., Orth A., Bonhomme F., Strack B., Guénet, Hameister H., Fundele R. An X-chromosome linked locus contributes to abnormal placental development in mouse interspecific hybrid. Nat Genet. 1996 Apr;12(4):398–403. doi: 10.1038/ng0496-398. [DOI] [PubMed] [Google Scholar]

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