|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Development, Vol 99, Issue 3 411-416, Copyright © 1987 by Company of Biologists
JOURNAL ARTICLES |
JR Mann and RH Lovell-Badge
MRC Mammalian Development Unit, University College London, UK.
Diploid gynogenetic embryos, which have two sets of maternal and no paternal chromosomes, die at or soon after implantation. Since normal female embryos preferentially inactivate the paternally derived X chromosome in certain extraembryonic membranes, the inviability of diploid gynogenetic embryos might be due to difficulties in achieving an equivalent inactivation of one of their two maternally derived X chromosomes. In order to investigate this possibility, we constructed XO gynogenetic embryos by nuclear transplantation at the 1-cell stage. These XO gynogenones showed the same mortality around the time of implantation as did their XX gynogenetic counterparts. This shows that the lack of a paternally derived autosome set is sufficient to cause gynogenetic inviability at this stage. Autosomal imprinting and its possible relation to X-chromosome imprinting is discussed.
This article has been cited by other articles:
![]() |
K. Sha and A. Fire Imprinting Capacity of Gamete Lineages in Caenorhabditis elegans Genetics, August 1, 2005; 170(4): 1633 - 1652. [Abstract] [Full Text] [PDF] |
||||
![]() |
Y Marahrens, B Panning, J Dausman, W Strauss, and R Jaenisch Xist-deficient mice are defective in dosage compensation but not spermatogenesis. Genes & Dev., January 15, 1997; 11(2): 156 - 166. [Abstract] [PDF] |
||||
![]() |
P E Szabo and J R Mann Biallelic expression of imprinted genes in the mouse germ line: implications for erasure, establishment, and mechanisms of genomic imprinting. Genes & Dev., August 1, 1995; 9(15): 1857 - 1868. [Abstract] [PDF] |
||||