| Literature DB >> 16235118 |
Edda Koina1, Matthew J Wakefield, Cristina Walcher, Christine M Disteche, Siobhan Whitehead, Mark Ross, Jennifer A Marshall Graves.
Abstract
X chromosome inactivation (XCI) achieves dosage compensation between males and females for most X-linked genes in eutherian mammals. It is a whole-chromosome effect under the control of the XIST locus, although some genes escape inactivation. Marsupial XCI differs from the eutherian process, implying fundamental changes in the XCI mechanism during the evolution of the two lineages. There is no direct evidence for the existence of a marsupial XIST homologue. XCI has been studied for only a handful of genes in any marsupial, and none in the model kangaroo Macropus eugenii (the tammar wallaby). We have therefore studied the sequence, location and activity of a gene SLC16A2 (solute carrier, family 16, class A, member 2) that flanks XIST on the human and mouse X chromosomes. A BAC clone containing the marsupial SLC16A2 was mapped to the end of the long arm of the tammar X chromosome and used in RNA FISH experiments to determine whether one or both loci are transcribed in female cells. In male and female cells, only a single signal was found, indicating that the marsupial SLC16A2 gene is silenced on the inactivated X.Entities:
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Year: 2005 PMID: 16235118 PMCID: PMC2819140 DOI: 10.1007/s10577-005-1006-5
Source DB: PubMed Journal: Chromosome Res ISSN: 0967-3849 Impact factor: 5.239