Comparative analysis of the mouse and human genes (Matn2 and MATN2) for matrilin-2, a filament-forming protein widely distributed in extracellular matrices

Lajos Mátés, Éva Korpos, Ferenc Deák, Zhanqin Liu, David R. Beier, Attila Aszódi, Ibolya Kiss

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

We previously identified matrilin-2 (MATN2), the largest member of the novel family of matrilins. These filament-forming adapter proteins expressed in a distinct, but partially overlapping, pattern in all tissues were implicated in the organization of the extracellular matrix. Matrilin-2 functions in a great variety of tissues. Here, we present the genomic organization of the highly conserved mouse and human MATN2 loci, which cover >100 kb and 167.167 kb genomic regions, respectively, and are composed of 19 exons. RT-PCR analysis revealed that alternative transcripts with identical protein coding regions are transcribed from two promoters in both species. The upstream, housekeeping type promoter is functional in all tissues and cell types tested. The activity of the downstream, TATA-like promoter preceded with putative motifs for the homeobox transcription factor PRRX2 is restricted to embryonic fibroblasts and certain cell lines. The oligomerization module is split by an U12-type AT-AC intron found in conserved position in all four matrilin genes. We assigned Matn2 to mouse chromosome 15, linked to Trhr and Sntb1 in a region synthenic to human chromosome 8q22-24.

Original languageEnglish
Pages (from-to)163-174
Number of pages12
JournalMatrix Biology
Volume21
Issue number2
DOIs
Publication statusPublished - Feb 28 2002

Keywords

  • AT-AC introns
  • Adapter protein
  • Alternative promoters
  • Extracellular matrix
  • Genomic organization
  • PRRX2 motifs

ASJC Scopus subject areas

  • Molecular Biology

Fingerprint Dive into the research topics of 'Comparative analysis of the mouse and human genes (Matn2 and MATN2) for matrilin-2, a filament-forming protein widely distributed in extracellular matrices'. Together they form a unique fingerprint.

  • Cite this