Literature DB >> 10198170

Invertebrate tissue inhibitor of metalloproteinase: structure and nested gene organization within the synapsin locus is conserved from Drosophila to human.

N Pohar1, T A Godenschwege, E Buchner.   

Abstract

Vertebrate tissue inhibitors of metalloproteinases (TIMPs) regulate extracellular matrix metalloproteinases and are thus involved in a wide variety of developmental and physiological processes. By identifying cDNAs of a transcript detected within an intron of the Drosophila synapsin gene we have cloned the Drosophila TIMP gene (Timp), which represents the first invertebrate member of the TIMP gene family. Sequence analysis revealed an open reading frame of 210 amino acids with 35% identity to human TIMPs and a conserved exon-intron structure. Analysis of sequence data from the Sanger Centre demonstrated that the human TIMP3 gene is encoded within intron V of the human synapsin-III gene, indicating that the nested organization of TIMP and synapsin genes may be a general feature conserved in evolution. We therefore speculate that the human TIMP4 gene will be located in intron V of the human synapsin-II gene on chromosome 3p25, and we present preliminary evidence that a human synapsin-IV gene is located near the TIMP2 gene on chromosome 17q23-q25. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10198170     DOI: 10.1006/geno.1999.5776

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  24 in total

1.  Genome-scale analysis of positionally relocated genes.

Authors:  Arjun Bhutkar; Susan M Russo; Temple F Smith; William M Gelbart
Journal:  Genome Res       Date:  2007-11-07       Impact factor: 9.043

Review 2.  The tissue inhibitors of metalloproteinases (TIMPs): an ancient family with structural and functional diversity.

Authors:  Keith Brew; Hideaki Nagase
Journal:  Biochim Biophys Acta       Date:  2010-01-15

Review 3.  Metalloproteinases and their tissue inhibitors in Alzheimer's disease and other neurodegenerative disorders.

Authors:  Santiago Rivera; Laura García-González; Michel Khrestchatisky; Kévin Baranger
Journal:  Cell Mol Life Sci       Date:  2019-06-13       Impact factor: 9.261

4.  Structural analysis of cDNAs coding for 4SNc-Tudor domain protein from fish and their expression in yellowtail organs.

Authors:  Shunnosuke Abe; Pi-Lin Wang; Fuminori Takahashi; Eiji Sasaki
Journal:  Mar Biotechnol (NY)       Date:  2005-08-23       Impact factor: 3.619

5.  Identification of an initiator-like element essential for the expression of the tissue inhibitor of metalloproteinases-4 (Timp-4) gene.

Authors:  David A Young; Blaine W Phillips; Caroline Lundy; Robert K Nuttall; Aileen Hogan; Gilbert A Schultz; Kevin J Leco; Ian M Clark; Dylan R Edwards
Journal:  Biochem J       Date:  2002-05-15       Impact factor: 3.857

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

Authors:  Diane M Jaworski; Micah Beem-Miller; Gentian Lluri; Ramiro Barrantes-Reynolds
Journal:  Physiol Genomics       Date:  2006-09-19       Impact factor: 3.107

7.  Association of synapsin 2 with schizophrenia in families of Northern European ancestry.

Authors:  Viatcheslav Saviouk; Michael P Moreau; Irina V Tereshchenko; Linda M Brzustowicz
Journal:  Schizophr Res       Date:  2007-09-04       Impact factor: 4.939

8.  The synapsin gene family in basal chordates: evolutionary perspectives in metazoans.

Authors:  Simona Candiani; Luca Moronti; Roberta Pennati; Fiorenza De Bernardi; Fabio Benfenati; Mario Pestarino
Journal:  BMC Evol Biol       Date:  2010-01-29       Impact factor: 3.260

9.  Cloning and expression of an inhibitor of microbial metalloproteinases from insects contributing to innate immunity.

Authors:  Anja Clermont; Marianne Wedde; Volkhard Seitz; Lars Podsiadlowski; Dido Lenze; Michael Hummel; Andreas Vilcinskas
Journal:  Biochem J       Date:  2004-08-15       Impact factor: 3.857

Review 10.  Tissue inhibitors of metalloproteinases in cell signaling: metalloproteinase-independent biological activities.

Authors:  William G Stetler-Stevenson
Journal:  Sci Signal       Date:  2008-07-08       Impact factor: 8.192

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