Frankowski Harald, Castro-Obregon Susana, del Rio Gabriel, Rao Rammohan V, Bredesen Dale E
Buck Institute for Age Research, Novato, CA 94945-1400, USA.
Neuromolecular Med. 2002;1(3):153-70. doi: 10.1385/NMM:1:3:153.
We describe the cloning and characterization of a rat single transmembrane protein that is homologous to the common neurotrophin receptor p75NTR in its death domain and the transmembrane region but dissimilar outside these regions. We have dubbed this protein PLAIDD, for p75-like apoptosis-inducing death domain protein. PLAIDD messenger RNA, which is ubiquitously distributed, is highly expressed in the embryo, but downregulated in adult tissues. Alternative splicing within the extracellular region of PLAIDD generates four RNA species, but only two of them are translated, PLAIDD_L and PLAIDD_S (long and short isoforms, respectively). While the amino acid sequence of the intracellular region of PLAIDD displays 41% identity with the intracellular region of p75NTR, the extracellular region of PLAIDD does not reveal any homology with p75NTR. Overexpression of each isoform of PLAIDD led to cytotoxicity in superior cervical ganglion neurons and in human embryonic kidney 293T cells. Both isoforms of PLAIDD could be co-immunoprecipitated with p75NTR, suggesting an interaction between these molecules.
我们描述了一种大鼠单跨膜蛋白的克隆和特性,该蛋白在其死亡结构域和跨膜区域与常见的神经营养因子受体p75NTR同源,但在这些区域之外则不同。我们将这种蛋白命名为PLAIDD,即p75样凋亡诱导死亡结构域蛋白。PLAIDD信使RNA广泛分布,在胚胎中高度表达,但在成年组织中下调。PLAIDD细胞外区域的可变剪接产生四种RNA种类,但其中只有两种被翻译,即PLAIDD_L和PLAIDD_S(分别为长和短异构体)。虽然PLAIDD细胞内区域的氨基酸序列与p75NTR的细胞内区域有41%的同一性,但PLAIDD的细胞外区域与p7定NTR没有任何同源性。PLAIDD的每种异构体的过表达都会导致颈上神经节神经元和人胚胎肾293T细胞产生细胞毒性。PLAIDD的两种异构体都可以与p75NTR进行共免疫沉淀,表明这些分子之间存在相互作用。