The characterization and localization of the mouse thymopoietin lamina-associated polypeptide 2 gene and its alternatively spliced products

被引:110
作者
Berger, R
Theodor, L
Shoham, J
Gokkel, E
BrokSimoni, F
Avraham, KB
Copeland, NG
Jenkins, NA
Rechavi, G
Simon, AJ
机构
[1] CHAIM SHEBA MED CTR, INST HEMATOL, IL-52621 TEL HASHOMER, ISRAEL
[2] TEL AVIV UNIV, SACKLER SCH MED, IL-69978 TEL AVIV, ISRAEL
[3] BAR ILAN UNIV, FAC LIFE SCI, RAMAT GAN, ISRAEL
[4] NCI, FREDERICK CANC RES & DEV CTR, ABL BASIC RES PROGRAM, MAMMALIAN GENET LAB, FREDERICK, MD 21702 USA
关键词
D O I
10.1101/gr.6.5.361
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Thymopoietins (Tmpos) are a group of ubiquitously expressed nuclear proteins, with sequence homology to lamina-associated polypeptide 2 (LAP2). Here we report the isolation and characterization of seven mouse Tmpo mRNA transcripts named Tmpo alpha, beta, beta', gamma, epsilon, delta, and zeta. The alpha, beta, and gamma Tmpo cDNA clones are the mouse homologs of the previously characterized human alpha, beta, and gamma TMPOs, respectively, whereas Tmpo epsilon, delta, and zeta are novel cDNAs. Additionally, the mouse Tmpo gene was cloned and characterized. It is a single-copy gene organized in 10 exons spanning similar to 22 kb, which encodes all of the described Tmpo cDNA sequences, located in the central region of mouse chromosome 10, The almost identical genomic organization between the human and mouse genes, and the novel alternatively spliced mouse transcripts, led us to reanalyze the human TMPO gene. The human beta-specific domain was found to be encoded by 3 exons designated 6a, 6b, and 6c and not by a single exon as described previously. These findings suggest that there may be more human transcripts than currently recognized, The possible involvement of the new growing family of Tmpo proteins in nuclear architecture and cell cycle control is discussed.
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页码:361 / 370
页数:10
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