Eberlé F, Dubreuil P, Mattei M G, Devilard E, Lopez M
INSERM U.119, Unité de Cancérologie et Thérapeutique Expérimentales, Marseille, France.
Gene. 1995 Jul 4;159(2):267-72. doi: 10.1016/0378-1119(95)00180-e.
Until now it was assumed that the murine poliovirus (PV) receptor homolog gene (MPH) had been identified. Alternative splicing of MPH transcripts generates two glycoproteins named MPH alpha and MPH beta which share an identical N-terminal region composed of three immunoglobulin (Ig)-like domains and different C-terminal regions. Using a degenerate PCR strategy, we describe the identification of a second human PVR-related gene (PRR2), which encodes two glycoproteins, PRR2 alpha (short form) and PRR2 delta (long form). They present 69 and 73% identity with MPH alpha and MPH beta, respectively. In contrast, the human PVR protein exhibits 51% identity which is moreover restricted to the three Ig domains of the murine protein. We therefore propose that PRR2, and not PVR, is the true human homolog of MPH. In addition, Northern blot analysis showed that two mRNA isoforms of 3.0 kb (PRR2 alpha) and 4.4 kb (PRR2 delta) are ubiquitously found in various normal human tissues. In situ hybridization allowed us to map PRR2 to the 19q13.2-q13.4 bands of the human genome, in the same chromosomal region as PVR.
直到现在,人们一直认为鼠源脊髓灰质炎病毒(PV)受体同源基因(MPH)已被鉴定出来。MPH转录本的可变剪接产生了两种糖蛋白,分别命名为MPHα和MPHβ,它们共享一个由三个免疫球蛋白(Ig)样结构域组成的相同N端区域和不同的C端区域。我们采用简并PCR策略,描述了第二个人类PVR相关基因(PRR2)的鉴定,该基因编码两种糖蛋白,PRR2α(短形式)和PRR2δ(长形式)。它们与MPHα和MPHβ的同一性分别为69%和73%。相比之下,人类PVR蛋白的同一性为51%,而且仅限于鼠源蛋白的三个Ig结构域。因此,我们提出PRR2而非PVR是MPH真正的人类同源物。此外,Northern印迹分析表明,3.0 kb(PRR2α)和4.4 kb(PRR2δ)的两种mRNA异构体在各种正常人体组织中普遍存在。原位杂交使我们能够将PRR2定位到人类基因组的19q13.2-q13.4带,与PVR位于同一染色体区域。