Literature DB >> 10373325

Identification and chromosomal location of two human genes encoding enzymes potentially involved in proteolytic maturation of farnesylated proteins.

J M Freije1, P Blay, A M Pendás, J Cadiñanos, P Crespo, C López-Otín.   

Abstract

Two human cDNAs encoding proteins similar to yeast enzymes involved in proteolytic processing of farnesylated proteins like a-factor mating pheromone and Ras2p have been cloned from an ovary cDNA library. These proteins have been tentatively called Face-1 and Face-2 (farnesylated protein-converting enzymes 1 and 2), respectively, and are integral membrane proteins, belonging to distinct families of metalloproteinases. Northern blot analysis of poly(A)+ RNAs isolated from a wide variety of human tissues demonstrated that both genes are expressed in all examined tissues, which suggests that these enzymes play housekeeping roles in normal processes. Fluorescence in situ hybridization experiments showed that the human FACE-1 gene maps to 1p34, whereas FACE-2 is located at 11q13, a region frequently amplified in human carcinomas and lymphomas. On the basis of these results, we suggest that inhibition of Face-1 and/or Face-2 could be part of strategies directed to block the functioning of prenylated proteins activated in oncogenic processes, including Ras proteins. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10373325     DOI: 10.1006/geno.1999.5834

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


  16 in total

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3.  Mutational analysis of the ras converting enzyme reveals a requirement for glutamate and histidine residues.

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5.  Identification, functional expression and enzymic analysis of two distinct CaaX proteases from Caenorhabditis elegans.

Authors:  Juan Cadiñanos; Walter K Schmidt; Antonio Fueyo; Ignacio Varela; Carlos López-Otín; José M P Freije
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Review 6.  Biogenesis of the Saccharomyces cerevisiae pheromone a-factor, from yeast mating to human disease.

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9.  A novel family of soluble minimal scaffolds provides structural insight into the catalytic domains of integral membrane metallopeptidases.

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Journal:  J Biol Chem       Date:  2013-06-03       Impact factor: 5.157

Review 10.  Accelerated ageing: from mechanism to therapy through animal models.

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