Leco K J, Apte S S, Taniguchi G T, Hawkes S P, Khokha R, Schultz G A, Edwards D R
Department of Medical Biochemistry, University of Calgary, Alberta, Canada.
FEBS Lett. 1997 Jan 20;401(2-3):213-7. doi: 10.1016/s0014-5793(96)01474-3.
We have isolated cDNA clones corresponding to a new member of the murine tissue inhibitor of metalloproteinase (TIMP) family, designated Timp-4. The nucleotide sequence predicts a protein of 22,609 Da that contains the characteristic 12 cysteine TIMP signature. TIMP-4 is more closely related to TIMP-2 and TIMP-3 than to TIMP-1 (48%, 45% and 38% identity, respectively). Analysis of Timp-4 mRNA expression in adult mouse tissues indicated a 1.2 kb transcript in brain, heart, ovary and skeletal muscle. This pattern of expression distinguishes Timp-4 from other Timps, suggesting that the TIMP-4 protein may be an important tissue-specific regulator of extracellular matrix remodelling.
我们已经分离出与小鼠金属蛋白酶组织抑制剂(TIMP)家族的一个新成员相对应的cDNA克隆,命名为Timp-4。核苷酸序列预测该蛋白分子量为22,609 Da,含有特征性的12个半胱氨酸TIMP签名。与TIMP-1相比,TIMP-4与TIMP-2和TIMP-3的关系更为密切(分别为48%、45%和38%的同源性)。对成年小鼠组织中Timp-4 mRNA表达的分析表明,在脑、心脏、卵巢和骨骼肌中有一个1.2 kb的转录本。这种表达模式使Timp-4与其他Timps区分开来,表明TIMP-4蛋白可能是细胞外基质重塑的重要组织特异性调节因子。