EHD2, EHD3, and EHD4 encode novel members of a highly conserved family of EH domain-containing proteins

被引:80
作者
Pohl, U
Smith, JS
Tachibana, I
Ueki, K
Lee, HK
Ramaswamy, S
Wu, Q
Mohrenweiser, HW
Jenkins, RB
Louis, DN
机构
[1] Massachusetts Gen Hosp, Dept Pathol, Mol Neurooncol Lab, Boston, MA 02129 USA
[2] Massachusetts Gen Hosp, Neurosurg Serv, Mol Neurooncol Lab, Boston, MA 02129 USA
[3] Harvard Univ, Sch Med, Boston, MA 02129 USA
[4] Mayo Clin & Mayo Fdn, Div Lab Genet, Rochester, MN 55905 USA
[5] Harvard Univ, Dept Cellular & Mol Biol, Cambridge, MA 02138 USA
[6] Univ Calif Lawrence Livermore Natl Lab, Livermore, CA 94550 USA
关键词
D O I
10.1006/geno.1999.6087
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Exon trapping from a bacterial artificial chromosome (BAC 78138) mapping to the 19q13.3 glioma tumor suppressor candidate region yielded two exons that recognized a 3.6-kb transcript on Northern blot, Screening of a human fetal brain cDNA library with these exons identified three novel genes, designated EHD2, EHD3, and EHD4, which are homologous to the recently characterized human EHD1 (testilin/HPAST) and its mouse homolog Ehd1, as well as to homologs in Drosophila (Past1) and Caenorhabditis elegans. Alignment of the predicted peptide sequences revealed striking similarities, with multiple conserved regions that include a nucleotide-binding consensus site at the N-terminus, a bipartite nuclear localization signal, and an eps15 homology (EH) protein-binding domain with an EF-hand motif at the C-terminus. The genes are specifically expressed, with EHD2 highly expressed in heart, EHD3 in brain and heart, and EHD4 in heart and pancreas. EHD2 was confirmed to originate from BAC 78138 at 19q13.3; radiation hybrid mapping localized EHD3 and EHD4 to 2p21 and 15q11.1, respectively; EHD1 has been previously mapped to 11q13. The three EHD1 paralogs therefore represent novel members of a family of human EH domain-containing proteins that may play a role in endocytosis and signaling. Mutation analysis of the five coding exons of EHD2 in gliomas failed to detect any tumor-specific alterations, thus indicating that EHD2 is an unlikely candidate for the 19q tumor suppressor gene. (C) 2000 Academic Press.
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页码:255 / 262
页数:8
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