Noguchi Masafumi, Honsho Masanori, Abe Yuichi, Toyama Ryusuke, Niwa Hajime, Sato Yoshiteru, Ghaedi Kamran, Rahmanifar Ali, Shafeghati Yousef, Fujiki Yukio
Graduate School of Systems Life Sciences, Kyushu University Graduate School, Higashi-ku, Fukuoka, Japan.
Department of Biology, Faculty of Sciences, Kyushu University Graduate School, Higashi-ku, Fukuoka, Japan.
J Hum Genet. 2014 Jul;59(7):387-92. doi: 10.1038/jhg.2014.39. Epub 2014 May 22.
Rhizomelic chondrodysplasia punctata (RCDP) is an autosomal recessive disorder due to the deficiency in ether lipid synthesis. RCDP type 1, the most prominent type, is caused by the dysfunction of the receptor of peroxisome targeting signal type 2, Pex7 (peroxisomal biogenesis factor 7), and the rest of the patients, RCDP types 2 and 3, have defects in peroxisomal enzymes catalyzing the initial two steps of alkyl-phospholipid synthesis, glyceronephosphate O-acyltransferase and alkylglycerone phosphate synthase (Agps). We herein investigated defects of two patients with RCDP type 3. Patient 1 had a novel missense mutation, T1533G, resulting in the I511M substitution in Agps. The plasmalogen level was mildly reduced, whereas the protein level and peroxisomal localization of Agps-I511M in fibroblasts were normal as in the control fibroblasts. Structure prediction analysis suggested that the mutated residue was located in the helix α15 on the surface of V-shaped active site tunnel in Agps, likely accounting for the mild defects of plasmalogen synthesis. These results strongly suggest that an individual with mildly affected level of plasmalogen synthesis develops RCDP. In fibroblasts from patient 2, the expression of AGPS mRNA and Agps protein was severely affected, thereby giving rise to the strong reduction of plasmalogen synthesis.
肢根型点状软骨发育不良(RCDP)是一种由于醚脂合成缺陷导致的常染色体隐性疾病。1型RCDP是最常见的类型,由过氧化物酶体靶向信号2型受体Pex7(过氧化物酶体生物发生因子7)功能障碍引起,其余患者,即2型和3型RCDP,在催化烷基磷脂合成最初两步的过氧化物酶体酶、甘油磷酸O - 酰基转移酶和烷基甘油磷酸合酶(Agps)中存在缺陷。我们在此研究了两名3型RCDP患者的缺陷。患者1有一个新的错义突变T1533G,导致Agps中I511M替代。缩醛磷脂水平轻度降低,而成纤维细胞中Agps - I511M的蛋白质水平和过氧化物酶体定位与对照成纤维细胞一样正常。结构预测分析表明,突变残基位于Agps中V形活性位点通道表面的α15螺旋上,可能是缩醛磷脂合成轻度缺陷的原因。这些结果有力地表明,缩醛磷脂合成水平轻度受影响的个体可发生RCDP。在患者2的成纤维细胞中,AGPS mRNA和Agps蛋白的表达受到严重影响,从而导致缩醛磷脂合成大幅减少。