Literature DB >> 1447210

Patterns of expression of the six alternatively spliced exons affecting the structures of the COL1 and NC2 domains of the alpha 1(XIII) collagen chain in human tissues and cell lines.

M Juvonen1, M Sandberg, T Pihlajaniemi.   

Abstract

Reverse transcription-polymerase chain reactions and RNA protection experiments were used to examine alternative splicing of the six exons 3B-5, 12, and 13 affecting the COL1 and NC2 domains of type XIII collagen in seven human tissues and four cell lines. Distinct differences in the proportions of the variant mRNAs were found. With respect to the COL1 domain, all studied samples contained mRNAs corresponding to the shortest COL1 variants of 57 and 66 residues, with the former variant being prominent in most samples. Most of the samples also contained notable amounts of mRNAs that corresponded to the longest COL1 variants, mainly those of 104 and 95 residues. Particularly the extent of inclusion of exon 12 and 13 sequences, encoding most of the NC2 domain, varied according to the type of tissue or cell analyzed. Bone, cartilage, and colon adenocarcinoma samples contained little or none of the mRNAs corresponding to the long NC2 variants, whereas in fibroblast, lung, muscle, and osteosarcoma cells, those mRNAs were the major variants. The relative proportions of the various combinations of exons 3B-5, 12, and 13 were evaluated in four of the RNA samples. Interestingly, each of these samples appeared to contain only one to three major combinations of the six exons, representing about 40% to nearly 100% of all variants.

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Year:  1992        PMID: 1447210

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  7 in total

1.  A short sequence in the N-terminal region is required for the trimerization of type XIII collagen and is conserved in other collagenous transmembrane proteins.

Authors:  A Snellman; H Tu; T Väisänen; A P Kvist; P Huhtala; T Pihlajaniemi
Journal:  EMBO J       Date:  2000-10-02       Impact factor: 11.598

Review 2.  Extracellular matrix components in intestinal development.

Authors:  P Simon-Assmann; M Kedinger; A De Arcangelis; V Rousseau; P Simo
Journal:  Experientia       Date:  1995-09-29

3.  Abnormal adherence junctions in the heart and reduced angiogenesis in transgenic mice overexpressing mutant type XIII collagen.

Authors:  M Sund; R Ylönen; A Tuomisto; R Sormunen; J Tahkola; A P Kvist; S Kontusaari; H Autio-Harmainen; T Pihlajaniemi
Journal:  EMBO J       Date:  2001-09-17       Impact factor: 11.598

4.  Lack of cytosolic and transmembrane domains of type XIII collagen results in progressive myopathy.

Authors:  A P Kvist; A Latvanlehto; M Sund; L Eklund; T Väisänen; P Hägg; R Sormunen; J Komulainen; R Fässler; T Pihlajaniemi
Journal:  Am J Pathol       Date:  2001-10       Impact factor: 4.307

5.  Integrin α11β1 is a receptor for collagen XIII.

Authors:  Jarkko Koivunen; Hongmin Tu; Antti Kemppainen; Padmanabhan Anbazhagan; Mikko A Finnilä; Simo Saarakkala; Jarmo Käpylä; Ning Lu; Anne Heikkinen; André H Juffer; Jyrki Heino; Donald Gullberg; Taina Pihlajaniemi
Journal:  Cell Tissue Res       Date:  2020-12-11       Impact factor: 5.249

6.  Membrane-associated collagens with interrupted triple-helices (MACITs): evolution from a bilaterian common ancestor and functional conservation in C. elegans.

Authors:  Hongmin Tu; Pirkko Huhtala; Hang-Mao Lee; Josephine C Adams; Taina Pihlajaniemi
Journal:  BMC Evol Biol       Date:  2015-12-14       Impact factor: 3.260

7.  Membrane associated collagen XIII promotes cancer metastasis and enhances anoikis resistance.

Authors:  Hui Zhang; Tricia Fredericks; Gaofeng Xiong; Yifei Qi; Piotr G Rychahou; Jia-Da Li; Taina Pihlajaniemi; Wei Xu; Ren Xu
Journal:  Breast Cancer Res       Date:  2018-10-01       Impact factor: 6.466

  7 in total

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