van Groningen J J, Egmond M R, Bloemers H P, Swart G W
Department of Biochemistry, University of Nijmegen, The Netherlands.
FEBS Lett. 1997 Mar 3;404(1):82-6. doi: 10.1016/s0014-5793(97)00098-7.
nmd, a novel gene, was isolated by applying the differential mRNA display method to human melanoma cell lines with different metastatic capacity. In a panel of 17 other human tumor cell lines, nmd RNA expression could only be detected at low levels in T24 (bladder carcinoma) and Caco-2 (colon adenocarcinoma). Furthermore, it was found in placenta and liver, but not in skin, colon, spleen, lung, muscle, prostate and kidney. Sequence analysis classified the nmd gene product as a new member of the enzyme family of lipases (almost 30% identity in amino acid sequence with other human lipases). Active site residues of lipases were conserved in NMD, but NMD lacks the regulatory lid domain, which controls entry to the active site in classical lipases. A similar deletion was earlier reported by others in the guinea pig pancreatic (phospho)lipase GPLRP2 and the phospholipase A1 from hornet venom (DolmI).
nmd是一个新基因,通过将差异mRNA显示方法应用于具有不同转移能力的人黑色素瘤细胞系而分离得到。在另外17种人肿瘤细胞系中,仅在T24(膀胱癌)和Caco-2(结肠腺癌)中能检测到低水平的nmd RNA表达。此外,在胎盘和肝脏中发现了它,但在皮肤、结肠、脾脏、肺、肌肉、前列腺和肾脏中未发现。序列分析将nmd基因产物归类为脂肪酶酶家族的新成员(与其他人脂肪酶的氨基酸序列有近30%的同一性)。脂肪酶的活性位点残基在NMD中是保守的,但NMD缺乏调节性盖子结构域,该结构域控制经典脂肪酶进入活性位点。其他人早些时候在豚鼠胰腺(磷酸)脂肪酶GPLRP2和黄蜂毒液中的磷脂酶A1(DolmI)中也报道了类似的缺失。