Temple University, School of Medicine, Philadelphia, PA 19140, U.S.A.
Cancer Genomics Proteomics. 2011 Sep-Oct;8(5):227-33.
We previously located a senescence gene locus (SEN6A), at chromosome 6q14-21 by a functional strategy using chromosome transfer into immortal ovarian tumor cells. To further elucidate the SEN6A locus, intact chromosome 6 or 6q was transferred into rat ovarian tumor cells and a panel of immortal revertant clones of senescent cells was generated. The panel of independent colonies as well as mixed populations of revertant cells was analyzed for the presence or absence of chromosome 6 specific markers. These investigations led to the identification of a fine deletion of approximately 1cM at chromosomal interval 6q16.3. A contiguous stretch containing five yeast artificial chromosome (YAC) clones was constructed across the deleted region. The non-chimeric YAC clones were retrofitted and transferred into mouse A9 cells by spheroplast fusion to generate YAC/A9 hybrids. YAC DNA present in YAC/A9 hybrids was subsequently transferred by microcell fusion into immortal tumor cells, and the hybrid cells were characterized for their senescence phenotype. Using this functional strategy, the transfer of YAC clone 966b10 was shown to restore senescence in both rat and human ovarian and breast tumor cells. Our results demonstrate that the SEN6A gene is carried on a 1 Mb YAC, 966b10, which maps at 6q16.3.
我们先前通过使用染色体转移到永生卵巢肿瘤细胞中的功能策略,定位到了 6 号染色体 q14-21 上的一个衰老基因座(SEN6A)。为了进一步阐明 SEN6A 基因座,我们将完整的 6 号染色体或 6q 转移到大鼠卵巢肿瘤细胞中,并生成了一组衰老细胞的独立永生回复克隆。对独立克隆组和回复细胞的混合群体进行分析,以确定是否存在 6 号染色体特异性标记物。这些研究导致鉴定出染色体 6q16.3 处大约 1cM 的精细缺失。构建了跨越缺失区域的包含五个酵母人工染色体(YAC)克隆的连续片段。对非嵌合 YAC 克隆进行 retrofitting,并通过原生质体融合将其转移到小鼠 A9 细胞中,以生成 YAC/A9 杂种。随后通过微细胞融合将 YAC 中的 DNA 转移到永生肿瘤细胞中,并对杂种细胞的衰老表型进行了特征分析。使用这种功能策略,表明 YAC 克隆 966b10 的转移可恢复大鼠和人卵巢和乳腺癌肿瘤细胞的衰老。我们的结果表明,SEN6A 基因位于携带在 1Mb YAC 966b10 上,该基因位于 6q16.3。