NRG2

From Wikipedia, the free encyclopedia


Neuregulin 2
Identifiers
Symbol(s) NRG2; Don-1; HRG2; NTAK
External IDs OMIM: 603818 HomoloGene75024
RNA expression pattern

More reference expression data

Orthologs
Human Mouse
Entrez 9542 n/a
Ensembl ENSG00000158458 n/a
Uniprot O14511 n/a
Refseq XM_001129975 (mRNA)
XP_001129975 (protein)
n/a (mRNA)
n/a (protein)
Location Chr 5: 139.21 - 139.4 Mb n/a
Pubmed search [1] n/a

Neuregulin 2, also known as NRG2, is a human gene.[1]

Neuregulin 2 (NRG2) is a novel member of the neuregulin family of growth and differentiation factors. Through interaction with the Erbb family of receptors, NRG2 induces the growth and differentiation of epithelial, neuronal, glial, and other types of cells. The gene consists of 12 exons and the genomic structure is similar to that of neuregulin 1 (NRG1), another member of the neuregulin family of ligands. NRG1 and NRG2 mediate distinct biological processes by acting at different sites in tissues and eliciting different biological responses in cells. The gene is located close to the region for demyelinating Charcot-Marie-Tooth disease locus, but is not responsible for this disease. Alternative transcripts encoding distinct isoforms have been described.[1]

[edit] References

[edit] Further reading

  • Chang H, Riese DJ, Gilbert W, et al. (1997). "Ligands for ErbB-family receptors encoded by a neuregulin-like gene.". Nature 387 (6632): 509–12. doi:10.1038/387509a0. PMID 9168114. 
  • Carraway KL, Weber JL, Unger MJ, et al. (1997). "Neuregulin-2, a new ligand of ErbB3/ErbB4-receptor tyrosine kinases.". Nature 387 (6632): 512–6. doi:10.1038/387512a0. PMID 9168115. 
  • Busfield SJ, Michnick DA, Chickering TW, et al. (1997). "Characterization of a neuregulin-related gene, Don-1, that is highly expressed in restricted regions of the cerebellum and hippocampus.". Mol. Cell. Biol. 17 (7): 4007–14. PMID 9199335. 
  • Higashiyama S, Horikawa M, Yamada K, et al. (1998). "A novel brain-derived member of the epidermal growth factor family that interacts with ErbB3 and ErbB4.". J. Biochem. 122 (3): 675–80. PMID 9348101. 
  • Reddy PH, Stockburger E, Gillevet P, Tagle DA (1998). "Mapping and characterization of novel (CAG)n repeat cDNAs from adult human brain derived by the oligo capture method.". Genomics 46 (2): 174–82. doi:10.1006/geno.1997.5044. PMID 9417904. 
  • Ring HZ, Chang H, Guilbot A, et al. (1999). "The human neuregulin-2 (NRG2) gene: cloning, mapping and evaluation as a candidate for the autosomal recessive form of Charcot-Marie-Tooth disease linked to 5q.". Hum. Genet. 104 (4): 326–32. PMID 10369162. 
  • Yamada K, Ichino N, Nishii K, et al. (2000). "Characterization of the human NTAK gene structure and distribution of the isoforms for rat NTAK mRNA.". Gene 255 (1): 15–24. PMID 10974560. 
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932. 
  • Nakano N, Higashiyama S, Ohmoto H, et al. (2004). "The N-terminal region of NTAK/neuregulin-2 isoforms has an inhibitory activity on angiogenesis.". J. Biol. Chem. 279 (12): 11465–70. doi:10.1074/jbc.M311045200. PMID 14722120. 
  • Ponomareva ON, Ma H, Dakour R, et al. (2005). "Stimulation of acetylcholine receptor transcription by neuregulin-2 requires an N-box response element and is regulated by alternative splicing.". Neuroscience 134 (2): 495–503. doi:10.1016/j.neuroscience.2005.04.028. PMID 15961242. 
  • Fan BJ, Ko WC, Wang DY, et al. (2007). "Fine mapping of new glaucoma locus GLC1M and exclusion of neuregulin 2 as the causative gene.". Mol. Vis. 13: 779–84. PMID 17563728.