Chesnel F, Hascoet P, Gagné J P, Couturier A, Jouan F, Poirier G G, Le Goff C, Vigneau C, Danger Y, Verite F, Le Goff X, Arlot-Bonnemains Y
CNRS-UMR 6290 (IGDR)-Université Rennes 1-BIOSIT, 2 Avenue du Professeur L Bernard, 35042 Rennes, France.
Centre de Recherche du CHU de Québec-Pavillon CHUL-Faculté de Médecine, Université Laval, 2705 Boulevard Laurier, Québec, G1V 4G2 QC, Canada.
Br J Cancer. 2015 Jul 14;113(2):336-44. doi: 10.1038/bjc.2015.189. Epub 2015 Jun 2.
The von Hippel-Lindau (VHL) gene encodes two mRNA variants. Variant 1 encodes two protein isoforms, pVHL213 and pVHL160, that have been extensively documented in the literature. Variant 2 is produced by alternative splicing of exon 2 and encodes a pVHL isoform of 172 amino acids with a theoretical molecular weight of 19 kDa (pVHL172), the expression of which has never been demonstrated so far due to the absence of suitable antibodies.
We have generated an anti-pVHL monoclonal antibody (JD-1956) using pVHL172 recombinant protein. We tested the antibody against exogenous or endogenous expressed proteins in different cell lines. We identified the pVHL172 using a silencing RNA strategy. The epitope of the antibody was mapped using a peptide array.
We efficiently detected the three different isoforms of pVHL in cell lines and tumorigenic tissues by western blotting and immunohistochemistry and confirmed for the first time the endogenous expression of pVHL172.
The endogenous expression of the three isoforms and particularly the pVHL172 has never been shown before due to a lack of a highly specific antibody since none of the available commercial antibodies distinguish the three isoforms of pVHL in cells or in both normal and cancerous human tissues. Evidence of pVHL172 expression emphasises the need to further study its implication in renal tumorigenesis and VHL disease.
冯·希佩尔-林道(VHL)基因编码两种mRNA变体。变体1编码两种蛋白质异构体,即pVHL213和pVHL160,已有大量文献记载。变体2是由外显子2的可变剪接产生的,编码一种含有172个氨基酸、理论分子量为19 kDa的pVHL异构体(pVHL172),由于缺乏合适的抗体,其表达至今尚未得到证实。
我们利用pVHL172重组蛋白制备了一种抗pVHL单克隆抗体(JD-1956)。我们在不同细胞系中针对外源或内源表达的蛋白对该抗体进行了检测。我们采用RNA干扰策略鉴定了pVHL172。利用肽阵列对该抗体的表位进行了定位。
我们通过蛋白质印迹法和免疫组织化学法在细胞系和致瘤组织中高效检测到了pVHL的三种不同异构体,并首次证实了pVHL172的内源性表达。
由于缺乏高特异性抗体,此前从未显示过这三种异构体尤其是pVHL172的内源性表达,因为现有的商业抗体均无法区分细胞或人体正常及癌组织中pVHL的三种异构体。pVHL172表达的证据强调了进一步研究其在肾肿瘤发生和VHL病中的作用的必要性。