Cousens Christina, Bishop Jeanette V, Philbey Adrian W, Gill Clare A, Palmarini Massimo, Carlson Jonathan O, DeMartini James C, Sharp J Michael
Moredun Research Institute, Pentlands Science Park, Bush Loan, Edinburgh EH26 0PZ, United Kingdom.
J Virol. 2004 Aug;78(16):8506-12. doi: 10.1128/JVI.78.16.8506-8512.2004.
Ovine pulmonary adenocarcinoma (OPA) is an infectious lung tumor of sheep caused by Jaagsiekte sheep retrovirus (JSRV). To test the hypothesis that JSRV insertional mutagenesis is involved in the oncogenesis of OPA, we cloned and characterized 70 independent integration sites from 23 cases of OPA. Multiple integration sites were identified in most tumors. BLAST analysis of the sequences did not disclose any potential oncogenic motifs or any identical integration sites in different tumors. Thirty-seven of the integration sites were mapped to individual chromosomes by PCR with a panel of sheep-hamster hybrid cell lines. Integration sites were found on 20 of the 28 sheep chromosomes, suggesting a random distribution. However, four integration sites from four different tumors mapped to chromosome 16. By Southern blot hybridization, probes derived from two of these sites mapped to within 5 kb of each other on normal sheep DNA. These sites were found within a single sheep bacterial artificial chromosome clone and were further mapped to only 2.5 kb apart, within an uncharacterized predicted gene and less than 200 kb from a mitogen-activated protein kinase-encoding gene. These findings suggest that there is at least one common integration site for JSRV in OPA and add weight to the hypothesis that insertional mutagenesis is involved in the development of this tumor.
绵羊肺腺癌(OPA)是由绵羊肺腺瘤逆转录病毒(JSRV)引起的绵羊传染性肺肿瘤。为了验证JSRV插入诱变参与OPA肿瘤发生的假说,我们从23例OPA中克隆并鉴定了70个独立的整合位点。在大多数肿瘤中都鉴定出多个整合位点。对这些序列进行BLAST分析,未在不同肿瘤中发现任何潜在的致癌基序或相同的整合位点。通过用一组绵羊 - 仓鼠杂交细胞系进行PCR,将37个整合位点定位到单个染色体上。在28条绵羊染色体中的20条上发现了整合位点,表明其分布是随机的。然而,来自四个不同肿瘤的四个整合位点定位到了16号染色体上。通过Southern印迹杂交,源自其中两个位点的探针在正常绵羊DNA上彼此相距5 kb以内。这些位点位于单个绵羊细菌人工染色体克隆内,并且进一步定位到相距仅2.5 kb,位于一个未表征的预测基因内,且距离一个丝裂原活化蛋白激酶编码基因不到200 kb。这些发现表明,在OPA中JSRV至少有一个共同的整合位点,这进一步支持了插入诱变参与该肿瘤发生发展的假说。