Literature DB >> 8046441

The developmental expression in rat of proteases furin, PC1, PC2, and carboxypeptidase E: implications for early maturation of proteolytic processing capacity.

M Zheng1, R D Streck, R E Scott, N G Seidah, J E Pintar.   

Abstract

The genes encoding mammalian subtilisin-like endoproteases furin, PC1, and PC2 have been isolated and are implicated in endoproteolytic cleavage of precursor molecules, which is a key step in posttranslational maturation of proproteins and neuropeptide precursors. Following endoproteolytic cleavage, the carboxyl-terminal basic amino acid residues are removed by carboxypeptidase E (CPE). We have examined the expression of these genes during rat development by in situ hybridization and compared their expression patterns to those of potential substrates. In the primitive streak stage of embryogenesis (e7) furin is expressed in both endoderm and mesoderm. This overall expression pattern is maintained until e10, when a distinctly higher level of furin expression is observed in the heart and liver primordia. In mid- and late gestational stages furin is broadly expressed in the peripheral tissues, and, therefore, may contribute to the proteolytic processing of numerous fetal proproteins, such as the precursors for natriuretic factors in heart and IGF-II throughout the embryo. In contrast, the expressions of PC1 and PC2 are initiated much later (e13) and are mainly confined to the developing nervous system, but with distinct spatial distributions. At midgestational ages, PC1 mRNA is mainly expressed in the hypothalamus and peripheral ganglia, while PC2 is expressed not only in these tissues but also in the thalamus, midbrain, pons, medulla oblongata, cortical plate, and spinal cord. Besides neuropeptide precursor processing in the nervous system, PC1 and PC2 may also be involved in the proteolytic processing in additional regions as evidenced by the finding that both PC1 and PC2 mRNAs are expressed in the embryonic pituitary and pancreas. CPE mRNA is expressed in both neural tissues and some non-neural tissues. In the developing nervous system, the expression of CPE encompasses all the regions where PC1 and PC2 are expressed and in fact includes most brain regions as neurogenesis proceeds. CPE mRNA is also expressed in some peripheral tissues, such as the embryonic heart and cartilage primordia, and in some cases its expression overlaps with furin expression. Thus, CPE may functionally collaborate during development with the subtilisin family of endoproteases in the completion of proteolytic processing of neuropeptide precursors in the nervous system and proproteins in the peripheral tissues. In the pituitary, the endoproteolytic processing of polyfunctional precursor proopiomelanocortin (POMC) occurs in a developmentally regulated manner. We have shown that while PC2 mRNA is predominantly expressed in the intermediate lobe in the adult, we observed an increased expression of PC2 mRNA in developing rat anterior lobe, peaking at early postnatal stages.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1994        PMID: 8046441      PMCID: PMC6577180     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  33 in total

Review 1.  New roles of carboxypeptidase E in endocrine and neural function and cancer.

Authors:  Niamh X Cawley; William C Wetsel; Saravana R K Murthy; Joshua J Park; Karel Pacak; Y Peng Loh
Journal:  Endocr Rev       Date:  2012-03-07       Impact factor: 19.871

2.  Identification and characterization of proSAAS, a granin-like neuroendocrine peptide precursor that inhibits prohormone processing.

Authors:  L D Fricker; A A McKinzie; J Sun; E Curran; Y Qian; L Yan; S D Patterson; P L Courchesne; B Richards; N Levin; N Mzhavia; L A Devi; J Douglass
Journal:  J Neurosci       Date:  2000-01-15       Impact factor: 6.167

3.  Neuropeptidomic analysis establishes a major role for prohormone convertase-2 in neuropeptide biosynthesis.

Authors:  Xin Zhang; Hui Pan; Bonnie Peng; Donald F Steiner; John E Pintar; Lloyd D Fricker
Journal:  J Neurochem       Date:  2009-12-07       Impact factor: 5.372

4.  The chemorepulsive activity of secreted semaphorins is regulated by furin-dependent proteolytic processing.

Authors:  R H Adams; M Lohrum; A Klostermann; H Betz; A W Püschel
Journal:  EMBO J       Date:  1997-10-15       Impact factor: 11.598

Review 5.  Molecular diversity in neurosecretion: reflections on the hypothalamo-neurohypophysial system.

Authors:  H Gainer; H Chin
Journal:  Cell Mol Neurobiol       Date:  1998-04       Impact factor: 5.046

Review 6.  Furin: a mammalian subtilisin/Kex2p-like endoprotease involved in processing of a wide variety of precursor proteins.

Authors:  K Nakayama
Journal:  Biochem J       Date:  1997-11-01       Impact factor: 3.857

7.  TGFbeta1 regulates gene expression of its own converting enzyme furin.

Authors:  F Blanchette; R Day; W Dong; M H Laprise; C M Dubois
Journal:  J Clin Invest       Date:  1997-04-15       Impact factor: 14.808

8.  BMP-4 is proteolytically activated by furin and/or PC6 during vertebrate embryonic development.

Authors:  Y Cui; F Jean; G Thomas; J L Christian
Journal:  EMBO J       Date:  1998-08-17       Impact factor: 11.598

9.  The adult boar testicular and epididymal transcriptomes.

Authors:  Benoît Guyonnet; Guillemette Marot; Jean-Louis Dacheux; Marie-José Mercat; Sandrine Schwob; Florence Jaffrézic; Jean-Luc Gatti
Journal:  BMC Genomics       Date:  2009-08-07       Impact factor: 3.969

10.  Zebrafish ProVEGF-C expression, proteolytic processing and inhibitory effect of unprocessed ProVEGF-C during fin regeneration.

Authors:  Abdel-Majid Khatib; Rachid Lahlil; Nathalie Scamuffa; Marie-Andrée Akimenko; Sylvain Ernest; Abdderahim Lomri; Claude Lalou; Nabil G Seidah; Bruno O Villoutreix; Fabien Calvo; Geraldine Siegfried
Journal:  PLoS One       Date:  2010-07-02       Impact factor: 3.240

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