HnRNP A3 genes and pseudogenes in the vertebrate genomes
β Scribed by Makeyev, Aleksandr V. ;Kim, Chang Bae ;Ruddle, Frank H. ;Enkhmandakh, Badam ;Erdenechimeg, Lkhamsuren ;Bayarsaihan, Dashzeveg
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 607 KB
- Volume
- 303A
- Category
- Article
- ISSN
- 1548-8969
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β¦ Synopsis
Abstract
The hnRNP A/B type proteins are abundant nuclear factors that bind to Pol II transcripts and are involved in numerous RNAβrelated activities. To date most data on the hnRNP A/B family have been obtained with recombinant proteins and cell cultures. Further characterization can result from an examination of the impact of various modifications in intact functional loci; however, such characterization is hampered by the presence of numerous and widely dispersed hnRNP A/Bβrelated sequences in the mammalian genome. We have found hnRNP A3, a poorly recognized member of the hnRNP A/B family, among candidate transcription factors that interact with the regulatory region of the Hoxc8 gene and screened the human and mouse genomes for genes that encode hnRNP A3. We demonstrate that the sequence reported previously as the human hnRNP A3 gene (Accession number S63912) and located on 10p11.1 belongs to a processed pseudogene of the functional intronβcontaining locus HNRPA3, which we have identified on 2q31.2. We have also identified its murine orthologs on mouse chromosome 2D and rat chromosome 3q23. Alternative splices were revealed at the Nβterminus and in the middle of hnRNP A3. 14 and 28 additional loci in the human and mouse genome, respectively, were mapped and identified as hnRNP A3 processed pseudogenes. In addition, we have found and compared hnRNP A3 orthologous genes in Gallus gallus, Xenopus tropicalis, and Danio rerio. The present in silico analysis serves as a necessary step toward a further functional characterization of hnRNP A3. J. Exp. Zool. 303A:259β271, 2005. Β© 2005 WileyβLiss, Inc.
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