IMR Press / FBL / Volume 14 / Issue 1 / DOI: 10.2741/3239

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with Frontiers in Bioscience.

Article

The fate of duplicated immunity genes in the dodecaploid Xenopus ruwenzoriensis

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1 University of Basel, Department of Zoology and Evolutionary Biology University of Basel Vesalgasse 1 CH-4051 Basel, Switzerland
2 2 University of Mississippi Medical Center, Department of Microbiology University of Mississippi Medical Center2500 North State StreetJackson, MS 39216-4505, USA
3 Washington University School of medicine in St-Louis Department of bone and mineral diseases 660 South Euclid Avenue, Campus Box 8301 St. Louis, MO 63110, USA
Front. Biosci. (Landmark Ed) 2009, 14(1), 177–191; https://doi.org/10.2741/3239
Published: 1 January 2009
Abstract

The relatively recent dodecaploid Xenopus (X.) ruwenzoriensis (108 chromosomes) permits to catch the phenomenon of gene silencing or modification in the act. This is interesting for genes related to the immune system, many of which can be selected as a consequence of their utility or eliminated as a consequence of their cost. Among receptor genes, a trend toward diploidization is seen: neither T cell receptor, Immunoglobulin, or Major Histocompatibility Complex Class I and II and linked loci are present on all paralogs. The fate of linked Class I and Class II loci can be independent from one another. Six Class II beta sequences can be detected in heterozygous X. laevis and X. ruwenzoriensis but they are distributed on two (disomic) loci in X. laevis versus 6 (polysomic) loci in X. ruwenzoriensis. In the same two species 2 Class I sequences can be detected in heterozygous X. laevis versus 4 in X. ruwenzoriensis. One interpretation is that natural selection acts more on the number of genes than on the mode of inheritance (polysomic versus disomic).

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