A unique human gene that spans over 230 kb in the human chromosome 8p11-12 and codes multiple family proteins sharing RNA-binding motifs

A unique gene, RBP-MS, spanning over 230 kb in the human chromosome 8p11-12 near the Werner syndrome gene locus is described. The single-copy RBP-MS gene is alternatively spliced, resulting in a family of at least 12 transcripts (average length of 1.5 kb). Nine different types of cDNAs that encode a...

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Bibliographic Details
Published in:	Proceedings of the National Academy of Sciences - PNAS Vol. 93; no. 20; pp. 10913 - 10917
Main Authors:	Shimamoto, A, Kitao, S, Ichikawa, K, Suzuki, N, Yamabe, Y, Imamura, O, Tokutake, Y, Satoh, M, Matsumoto, T, Kuromitsu, J, Kataoka, H, Sugawara, K, Sugawara, M, Sugimoto, M, Goto, M, Furuichi, Y
Format:	Journal Article
Language:	English
Published:	United States National Acad Sciences 01-10-1996
Subjects:	Alternative Splicing Amino Acid Sequence Base Sequence Chromosomes, Human, Pair 8 Cloning, Molecular Drosophila Exons Gene Expression Genes Humans Introns Molecular Sequence Data RNA, Messenger - genetics RNA-Binding Proteins - genetics Sequence Alignment Sequence Homology, Amino Acid Tissue Distribution Werner Syndrome - genetics
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