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      Biogenesis of secretory granules in the trans-Golgi network of neuroendocrine and endocrine cells

      research-article
      *
      Biochimica et Biophysica Acta. Molecular Cell Research
      Elsevier Science B.V.
      Secretion, Regulated secretion, trans-Golgi network, Vesicle formation, Immature secretory granule, TGN, trans-Golgi network, ISG, immature secretory granule, MSG, mature secretory granule, CSV, constitutive secretory vesicle, CCV, clathrin-coated vesicle, CgB, chromogranin B, SgII, secretogranin II, hsPG, heparan sulphate proteoglycan, PCs, prohormone converting enzymes, LDCV, large dense core vesicles, DTT, dithiothreitol, ARF, ADP-ribosylation factor, AP-1, adaptor protein-1, PLD, phospholipase D, GH, growth hormone, PRL, prolactin, MPR, mannose-6-phosphate receptor, PIP2 (phosphatidylinositol 4,5-bisphosphate), PITP, phosphatidylinositol transfer protein, PI, phosphatidylinositol

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          Abstract

          Secretory granule formation requires selection of soluble and membrane proteins into nascent secretory granules, and exclusion of proteins not required for the function of secretory granules. Both selection and exclusion presumably can occur in the compartment where assembly of the secretory granule begins, the trans most cisternae of the Golgi complex. Current research focused on the initial stages of secretory granule formation includes a search for the ‘signals’ which may mediate active sorting of components into secretory granules, and the role of aggregation of regulated secretory proteins in sorting. In addition, the temporal sequence of the sorting events in the Golgi, and post-Golgi compartments has gained much attention, as summarized by the alternative but not mutually exclusive ‘sorting for entry’ vs. ‘sorting by retention’ models. ‘Sorting for entry’ which encompasses the most popular models requires selection of cargo and membrane and exclusion of non-secretory granule proteins in the TGN prior to secretory granule formation. ‘Sorting by retention’ stipulates that protein selection or exclusion may occur after secretory granule formation: secretory granule specific components are retained during maturation of the granule while non-secretory granule molecules are removed in vesicles which bud from maturing secretory granules. Finally, some progress has been made in the identification of cytosolic components involved in the budding of nascent secretory granules from the TGN. This review will focus on the recent data concerning the events in secretory granule formation which occur, in the trans-Golgi network.

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          Most cited references104

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          A presynaptic inositol-5-phosphatase.

          Synaptojanin is a nerve terminal protein of relative molecular mass 145,000 which appears to participate with dynamin in synaptic vesicle recycling. The central region of synaptojanin defines it as a member of the inositol-5-phosphatase family, which includes the product of the gene that is defective in the oculocerebrorenal syndrome of Lowe. Synaptojanin has 5-phosphatase activity and its amino-terminal domain is homologous with the yeast protein Sac1 (Rsd1), which is genetically implicated in phospholipid metabolism and in the function of the actin cytoskeleton. The carboxy terminus, which is of different lengths in adult and developing neurons owing to the alternative use of two termination sites, is proline-rich, consistent with the reported interaction of synaptojanin with the SH3 domains of Grb2 (refs 1, 2). Synaptojanin is the only other major brain protein besides dynamin that binds the SH3 domain of amphiphysin, a presynaptic protein with a putative function in endocytosis. Our results suggest a link between phosphoinositide metabolism and synaptic vesicle recycling.
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            Hyperproinsulinaemia in obese fat/fat mice associated with a carboxypeptidase E mutation which reduces enzyme activity.

            Mice homozygous for the fat mutation develop obesity and hyperglycaemia that can be suppressed by treatment with exogenous insulin. The fat mutation maps to mouse chromosome 8, very close to the gene for carboxypeptidase E (Cpe), which encodes an enzyme (CPE) that processes prohormone intermediates such as proinsulin. We now demonstrate a defect in proinsulin processing associated with the virtual absence of CPE activity in extracts of fat/fat pancreatic islets and pituitaries. A single Ser202Pro mutation distinguishes the mutant Cpe allele, and abolishes enzymatic activity in vitro. Thus, the fat mutation represents the first demonstration of an obesity-diabetes syndrome elicited by a genetic defect in a prohormone processing pathway.
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              The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase.

              Lowe's oculocerebrorenal syndrome (OCRL) is a human X-linked developmental disorder of unknown pathogenesis and has a pleiotropic phenotype affecting the lens, brain and kidneys. The OCRL locus has been mapped to Xq25-q26 by linkage and by finding de novo X; autosome translocations at Xq25-q26 in two unrelated females with OCRL. Here we use yeast artificial chromosomes with inserts that span the X chromosomal breakpoint from a female OCRL patient in order to isolate complementary DNAs for a gene that is interrupted by the translocation. We show that the transcript is absent in both female OCRL patients with X; autosome translocations and that it is absent or abnormally sized in 9 of 13 unrelated male OCRL patients with no detectable genomic rearrangement. The open reading frame encodes a new protein with 71% similarity to human inositol polyphosphate-5-phosphatase. Our results suggest that OCRL may be an inborn error of inositol phosphate metabolism.
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                Author and article information

                Contributors
                Journal
                Biochim Biophys Acta Mol Cell Res
                Biochim Biophys Acta Mol Cell Res
                Biochimica et Biophysica Acta. Molecular Cell Research
                Elsevier Science B.V.
                0167-4889
                1879-2596
                23 December 1998
                14 August 1998
                23 December 1998
                : 1404
                : 1
                : 231-244
                Affiliations
                Secretory Pathways Laboratory, Imperial Cancer Research Fund, 44 Lincoln’s Inn Fields, London, WC2A 3PX, UK
                Author notes
                [* ]Fax: +44 (171) 269-3417; tooze@ 123456icrf.icnet.uk
                Article
                S0167-4889(98)00059-7
                10.1016/S0167-4889(98)00059-7
                7126647
                9714820
                bb0d2d64-9375-4b96-8949-09d189e7edf2
                Copyright © 1998 Elsevier Science B.V. All rights reserved.

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

                History
                : 20 November 1997
                : 19 December 1997
                Categories
                Article

                secretion,regulated secretion,trans-golgi network,vesicle formation,immature secretory granule,tgn, trans-golgi network,isg, immature secretory granule,msg, mature secretory granule,csv, constitutive secretory vesicle,ccv, clathrin-coated vesicle,cgb, chromogranin b,sgii, secretogranin ii,hspg, heparan sulphate proteoglycan,pcs, prohormone converting enzymes,ldcv, large dense core vesicles,dtt, dithiothreitol,arf, adp-ribosylation factor,ap-1, adaptor protein-1,pld, phospholipase d,gh, growth hormone,prl, prolactin,mpr, mannose-6-phosphate receptor,pip2 (phosphatidylinositol 4,5-bisphosphate),pitp, phosphatidylinositol transfer protein,pi, phosphatidylinositol

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