Literature DB >> 2121613

Cloning and structural analysis of a gene encoding a mouse mastocytoma proteoglycan core protein; analysis of its evolutionary relation to three cross hybridizing regions in the mouse genome.

T Angerth1, R Y Huang, M Aveskogh, I Pettersson, L Kjellén, L Hellman.   

Abstract

Serglycin (SGC) is a Ser-Gly-repeat-containing protein, used as a proteoglycan core protein in the parietal yolk sac and in mast cells, where glycosaminoglycan side chains are attached to the serine residues of the repeat region. In this article, the structure of the gene SGC encoding mouse SGC is reported. The gene is divided into three exons, which are all contained within a region of approximately 13 kb. Nucleotide (nt) sequence analysis was carried out on a region of 1.2 kb upstream from the first exon. The region containing the two promoters (active in parietal yolk sac and in mast cells, respectively) was analyzed for the presence of recognition sites for known DNA-binding proteins. A number of sequences closely related to known recognition sites were found in both promoters, and one consensus octamer-binding site could be identified in the putative yolk-sac promoter. Multiple regions in the mouse genome hybridizing with DNA fragments covering the Ser-Gly repeat region have previously been described, and it has been suggested that these loci may represent other proteoglycan core proteins. Analysis of nt sequence was carried out on three out of the more than 15 of these regions present in the mouse genome. However, none of the clones analyzed was found to have any open reading frame in the region of cross-hybridization which possibly could code for a SGC protein. Instead, one of the clones was found to contain an exon encoding a highly basic protein, unrelated to SGC. Hence, no evidence was found for a multigene family of Ser-Gly-repeat-containing proteoglycan-encoding genes.

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Year:  1990        PMID: 2121613     DOI: 10.1016/0378-1119(90)90230-o

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  8 in total

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Authors:  H Kresse; H Hausser; E Schönherr
Journal:  Experientia       Date:  1993-05-15

Review 2.  Mast Cell and Basophil Granule Proteases - In Vivo Targets and Function.

Authors:  Lars Hellman; Srinivas Akula; Zhirong Fu; Sara Wernersson
Journal:  Front Immunol       Date:  2022-07-05       Impact factor: 8.786

3.  Secretory granule proteases in rat mast cells. Cloning of 10 different serine proteases and a carboxypeptidase A from various rat mast cell populations.

Authors:  C Lützelschwab; G Pejler; M Aveskogh; L Hellman
Journal:  J Exp Med       Date:  1997-01-06       Impact factor: 14.307

4.  Loss of Serglycin Promotes Primary Tumor Growth and Vessel Functionality in the RIP1-Tag2 Mouse Model for Spontaneous Insulinoma Formation.

Authors:  Andrew Hamilton; Vladimir Basic; Sandra Andersson; Magnus Abrink; Maria Ringvall
Journal:  PLoS One       Date:  2015-05-15       Impact factor: 3.240

Review 5.  Tracing the Origins of IgE, Mast Cells, and Allergies by Studies of Wild Animals.

Authors:  Lars Torkel Hellman; Srinivas Akula; Michael Thorpe; Zhirong Fu
Journal:  Front Immunol       Date:  2017-12-19       Impact factor: 7.561

6.  Molecular Interactions Stabilizing the Promatrix Metalloprotease-9·Serglycin Heteromer.

Authors:  Rangita Dawadi; Nabin Malla; Beate Hegge; Imin Wushur; Eli Berg; Gunbjørg Svineng; Ingebrigt Sylte; Jan-Olof Winberg
Journal:  Int J Mol Sci       Date:  2020-06-12       Impact factor: 5.923

7.  Quantitative In-Depth Analysis of the Mouse Mast Cell Transcriptome Reveals Organ-Specific Mast Cell Heterogeneity.

Authors:  Srinivas Akula; Aida Paivandy; Zhirong Fu; Michael Thorpe; Gunnar Pejler; Lars Hellman
Journal:  Cells       Date:  2020-01-14       Impact factor: 6.600

8.  How Relevant Are Bone Marrow-Derived Mast Cells (BMMCs) as Models for Tissue Mast Cells? A Comparative Transcriptome Analysis of BMMCs and Peritoneal Mast Cells.

Authors:  Srinivas Akula; Aida Paivandy; Zhirong Fu; Michael Thorpe; Gunnar Pejler; Lars Hellman
Journal:  Cells       Date:  2020-09-17       Impact factor: 6.600

  8 in total

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