Characterization of the human NDRG gene family: A newly identified member,NDRG4, is specifically expressed in brain and heart

Citation
Rh. Zhou et al., Characterization of the human NDRG gene family: A newly identified member,NDRG4, is specifically expressed in brain and heart, GENOMICS, 73(1), 2001, pp. 86-97
Citations number
25
Categorie Soggetti
Molecular Biology & Genetics
Journal title
GENOMICS
ISSN journal
08887543 → ACNP
Volume
73
Issue
1
Year of publication
2001
Pages
86 - 97
Database
ISI
SICI code
0888-7543(20010401)73:1<86:COTHNG>2.0.ZU;2-P
Abstract
RTP/Drg1/Cap43/rit42/TDD5/Ndr1/N13RGI (referred to as NDRG1 hereafter) is a cytoplasmic protein involved in stress responses, hormone responses, cell growth, and differentiation. Recently, the mutation of this gene was report ed to be causative for hereditary motor and sensory neuropathy-Lom. Here, w e cloned two human cDNAs encoding NDRG3 and NDRG4, which are homologous to NDRG1. These two genes, together with NDRG1 and a previously deposited cDNA (designated NDRG2), constitute the NDRG gene family. The four members shar e 57-65% amino acid identity. NDRG4 was further characterized because its m RNA expression was quite specific in brain and heart, in contrast to the re latively ubiquitous expression of the other three members. NDRG4 mRNA consi sts of three isoforms, NDRG4-B, NDRG4-B-var, and NDRG4-H. Northern and West ern blot analyses showed that NDRG4-B was expressed only in the brain, wher eas NDRG4-H was expressed in both brain and heart. NDRG4-B-var was a minor product. NDRG4 expression was more abundant in adult than fetal brain and h eath and was markedly decreased in the Alzheimer's diseased brain. In situ hybridization showed that NDRG4 was localized in neurons of the brain and s pinal cord. The NDRG4 gene contains 17 exons. mRNA expression of the three NDRG4 isoforms is regulated by alternative splicing and possibly by alterna tive promoter usage. The finely tuned expression of the NDRG gene family me mbers suggests that they have different specific functions, (C) 2001 Academ ic Press.