Skewed X-chromosome inactivation in human embryos with mosaic trisomy 16

Russian Journal of Genetics

Volumn 47, Issue 3, 2011, Pages 354-357

  Tolmacheva, E N ^a   Kashevarova, A A ^a   Sukhanova, N N ^a   Kharkov, V N ^a   Lebedev, I N ^a  

^a RESEARCH INSTITUTE OF MEDICAL GENETICS   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; EMBRYO; EMBRYO MEMBRANE; FEMALE; HUMAN; HUMAN TISSUE; KARYOTYPE; MESODERM; PLACENTA; PRIORITY JOURNAL; SEX RATIO; SPONTANEOUS ABORTION; SURVIVAL; TRISOMY 16; X CHROMOSOME INACTIVATION;

EID: 79953009350     PISSN: 10227954     EISSN: 16083369     Source Type: Journal    
DOI: 10.1134/S1022795411020189     Document Type: Article

References (17)

1. Migeon, B. R., Pappas, K., Stetten, G., et al., X Inactivation in Triploidy and Trisomy: The Search for Autosomal Transfactors That Choose Active X, Eur. J. Hum. Genet., 2008, vol. 16, pp. 153-162.
2. Lau, A. W., Brown, C. J., Penaherrera, M. S., et al., Skewed X-Chromosome Inactivation Is Common in Fetuses or Newborns Associated with Confined Placental Mosaicism, Am. J. Hum. Genet., 1997, vol. 61, pp. 1353-1361.
3. Penaherrera, M. S., Barrett, I. J., Brown, C. J., et al., An Association between Skewed X-Chromosome Inactivation and Abnormal Outcome in Mosaic Trisomy 16 Confined Predominantly to the Placenta, Clin. Genet., 2000, vol. 58, pp. 436-446.
4. Langlois, S., Yong, P., Yong, S., et al., Postnatal Follow-up of Prenatally Diagnosed Trisomy 16 Mosaicism, Prenatal Diagn., 2006, vol. 26, pp. 548-558.
5. Lebedev, I. N., Ostroverkhova, N. V., Nikitina, T. V., et al., Features of Chromosomal Abnormalities in Spontaneous Abortion Cell Culture Failures Detected by Interphase FISH Analysis, Eur. J. Hum. Genet., 2004, vol. 12, pp. 513-520.
6. Mutter, G. L. and Boynton, K. A., PCR Bias in Amplification of Androgen Receptor Alleles, a Trinucleotide Repeat Marker Used in Clonality Studies, Nucl. Acids Res., 1995, vol. 23, pp. 1411-1418.
7. Minks, J., Robinson, W. P., and Brown, C. J., A Skewed View of X Chromosome Inactivation, J. Clin. Invest., 2008, vol. 118, pp. 20-23.
8. Vorsanova, S., Kolotii, A., Iourov, I., et al., Evidence for High Frequency of Chromosomal Mosaicism in Spontaneous Abortions Revealed by Interphase FISH Analysis, J. Histochem. Cytochem., 2005, vol. 53, no. 3, pp. 375-380.
9. Nazarenko, S. A., Timoshevskii, V. A., and Ostroverkhova, N. V., X-Interphase Analysis of X-Aneuploidy by the Fluorescence in situ Hybridization in Various Tissues of Healthy Individuals, Russ. J. Genet., 1997, vol. 33, no. 10, pp. 1222-1225.
10. Benn, P., Trisomy 16 and Trisomy 16 Mosaicism: A Review, Am. J. Med. Genet., 1998, vol. 79, pp. 121-133.
11. Yong, P., Barrett, I., Kalousek, D., and Robinson, W., Clinical Aspects, Prenatal Diagnosis, and Pathogenesis of Trisomy 16 Mosaicism, J. Med. Genet., 2003, vol. 40, pp. 175-182.
12. Evdokimova, V. N., Nikitina, T. V., Lebedev, I. N., et al., Sex Ratio in Early Embryonal Mortality in Humans, Ontogenez, 2000, vol. 31, no. 4, pp. 251-257.
13. Vasques, L. R., Klocker, M. N., and Pereira, L. V., X Chromosome Inactivation: How Human Are Mice?, Cytogenet. Genome Res., 2002, vol. 99, pp. 30-35.
14. Tolmacheva, E. N., Kashevarova, A. A., and Lebedev, I. N., Inactivation of X-Chromosome and Human Pathology, Med. Genet., 2009, vol. 8, no. 7, pp. 9-15.
15. Chao, W., Huynh, K. D., Spencer, R. J., et al., CTCF, a Candidate Trans-Action Factor for X-Inactivation Choice, Science, 2002, vol. 295, pp. 345-347.
16. Burke, L. J., Zhang, R., Bartkuhn, M., et al., CTCF Binding and Higher Order Chromatin Structure of the H19 Locus Are Maintained in Mitotic Chromatin, EMBO J., 2005, vol. 24, pp. 3291-3300.
17. Tada, T., Obata, Y., Tada, M., et al., Imprint Switching for Non-Random X-Chromosome Inactivation during Mouse Oocyte Growth, Development, 2000, vol. 127, pp. 3101-3103.