Mátés Lajos, Korpos Eva, Déak Ferenc, Liu Zhanqin, Beier David R, Aszódi Attila, Kiss Ibolya
Institute of Biochemistry, Biological Research Center of the Hungarian Academy of Sciences, P.O. Box 521, H-6701 Szeged, Hungary.
Matrix Biol. 2002 Mar;21(2):163-74. doi: 10.1016/s0945-053x(01)00194-9.
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.
我们之前鉴定出了基质金属蛋白酶-2(MATN2),它是基质金属蛋白酶新家族中最大的成员。这些在所有组织中以独特但部分重叠的模式表达的丝状形成衔接蛋白与细胞外基质的组织有关。基质金属蛋白酶-2在多种组织中发挥作用。在此,我们展示了高度保守的小鼠和人类MATN2基因座的基因组结构,它们分别覆盖大于100 kb和167.167 kb的基因组区域,由19个外显子组成。逆转录-聚合酶链反应(RT-PCR)分析表明,在两个物种中,具有相同蛋白质编码区的可变转录本从两个启动子转录而来。上游的管家型启动子在所有测试的组织和细胞类型中都有功能。下游的类TATA启动子之前有同源盒转录因子PRRX2的假定基序,其活性仅限于胚胎成纤维细胞和某些细胞系。寡聚化模块被一个U12型AT-AC内含子隔开,该内含子在所有四个基质金属蛋白酶基因的保守位置都能找到。我们将Matn2定位于小鼠15号染色体,在与人类8号染色体q22-24同区域的一个区域中与Trhr和Sntb1连锁。