作者: Siradanahalli C. Guru , Nijaguna B. Prasad , Eun J. Shin , Kirugaval Hemavathy , Jining Lu
DOI: 10.1016/S0378-1119(00)00562-X
关键词: Polyadenylation 、 Nuclear protein 、 Missense mutation 、 Gene 、 Drosophila melanogaster 、 Genetics 、 Transcription factor 、 Transcription (biology) 、 MEN1 、 Biology
摘要: Abstract Multiple endocrine neoplasia type 1 (MEN1) is a familial cancer syndrome characterized by tumors of the parathyroid, entero-pancreatic neuroendocrine and pituitary tissues caused inactivating mutations in MEN1 gene. Menin, 610-amino acid nuclear protein encoded , binds to transcription factor JunD can repress JunD-induced transcription. We report here identification ortholog Drosophila melanogaster Menin1 that encodes 763 amino sharing 46% identity with human menin. Additionally, 69% missense in-frame deletions reported patients appear residues are identical protein, suggesting importance conserved regions. gene transcripts use alternative polyadenylation sites resulting 4.3 5-kb messages. The 4.3-kb transcript appears be largely maternal, while mainly zygotic. binding menin or Jun could not demonstrated yeast two-hybrid analysis. from will provide an opportunity utilize genetics enhance our understanding function