作者: F.J. Benham , S. Hodgkinson , K.E. Davies
DOI: 10.1002/J.1460-2075.1984.TB02186.X
关键词: Homology (biology) 、 Pseudogene 、 X chromosome 、 Biology 、 Molecular biology 、 Protein sequencing 、 Complementary DNA 、 Gene 、 Peptide sequence 、 Nucleic acid thermodynamics 、 Genetics
摘要: A human X chromosome-derived gene sequence which recognises an abundant, 1.2-kb mRNA in several cell types was previously isolated during a study to identify expressed sequences from chromosome recombinant library. Further characterisation of this clone, acronym OA1, has shown that it maps the short arm X, at Xp21 Xp22. 777-bp fragment clone hybridizes been sequenced, and inferred amino acid shows 80% homology with published protein for muscle glyceraldehyde-3-phosphate dehydrogenase (GAPDH). The even higher (87%) pig GAPDH. OA1 selects translates vitro into polypeptide 36 K, subunit size However, X-sequence is most probably pseudogene whose structure consistent having arisen by reverse transcription GAPDH or GAPDH-related followed insertion chromosome. portion DNA fragments mouse DNA, six fibroblast cDNA clones cross-hybridize same genomic as OA1. This series identifies new, conserved multigene family.