Physiol. Genomics AJP: Cell Physiology
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Physiol. Genomics 28: 168-178, 2007. First published September 19, 2006; doi:10.1152/physiolgenomics.00160.2006
1094-8341/07 $8.00
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Received 21 July 2006; accepted in final form 16 September 2006.
Physiological Genomics 28:168-178 (2007)
1094-8341/07 $8.00 © 2007 American Physiological Society

Potential regulatory relationship between the nested gene DDC8 and its host gene tissue inhibitor of metalloproteinase-2

Diane M. Jaworski1, Micah Beem-Miller1, Gentian Lluri1 and Ramiro Barrantes-Reynolds2

1 Departments of Anatomy & Neurobiology, University of Vermont College of Medicine, Burlington, Vermont
2 Departments of Microbiology & Molecular Genetics, University of Vermont College of Medicine, Burlington, Vermont

Nested genes are fairly common within the mammalian nervous system, yet few studies have examined whether the guest and host genes might be coordinately regulated. Tissue inhibitors of metalloproteinase (TIMPs) inhibit extracellular matrix proteolysis mediated by metzincin proteases. TIMP-2 is the only TIMP not nested within a synapsin gene. It does, however, serve as a host for differential display clone 8 (DDC8), a testis-specific gene whose expression is upregulated during spermatogenesis. Here, we demonstrate that DDC8 is not testis specific. Furthermore, DDC8 expression in nonneural and neural tissues mimics that of TIMP-2, including its upregulation in response to traumatic brain injury, suggesting a potential regulatory relationship. The most striking observation is that the TIMP-2 knockout mouse brain contains TIMP-2 mRNA encoding exons 2–5, which are downstream of DDC8, but not exon 1, which contains the signal sequence and cysteine residue required for MMP inhibition, indicating a functional knockout. That TIMP-2 transcripts in wild-type brain contain DDC8 sequence suggests alternative splicing between the two genes.

alternative splicing; gene nesting; knockout; differential display clone 8




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W. G. Stetler-Stevenson
Tissue Inhibitors of Metalloproteinases in Cell Signaling: Metalloproteinase-Independent Biological Activities
Sci. Signal., July 8, 2008; 1(27): re6 - re6.
[Abstract] [Full Text] [PDF]




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