Kim M G, Schuler W, Bosma M J, Marcu K B
Genetics Graduate Program, SUNY, Stony Brook 11794-5215.
J Immunol. 1988 Aug 15;141(4):1341-7.
Studies of Ig and TCR genes in transformed lymphocytes of scid mice have revealed aberrant DNA rearrangements. Here we present a more detailed analysis of the Igh gene recombination in nine scid pre-B cell lines transformed by Abelson murine leukemia virus. We found 85% of the rearranged Igh alleles to contain abnormal Dh-Jh deletions of varying size. All of these deletions encompassed Jh elements and extended into the Igh enhancer region, occasionally involving the switch (S) region of the C mu gene. Some of these rearrangements removed most of the Dh elements, but none appeared to extend to the Vh genes. DNA sequence analysis of the two abnormally rearranged Igh alleles in one pre-B cell line showed that no Dh or Jh coding sequences were retained at the recombination sites though heptamer-like (CACTGTG) recognition signal sequences were present in the absence of nonamer (GGTTTTTGT) recognition signal sequences. These results imply that a deregulated recombinase activity may be responsible for the abnormal Dh-Jh deletions and the absence of Vh-Dh joining in established lines of Abelson murine leukemia virus-transformed scid pre-B cells.
对重症联合免疫缺陷(scid)小鼠转化淋巴细胞中免疫球蛋白(Ig)和T细胞受体(TCR)基因的研究已揭示出异常的DNA重排。在此,我们对由阿贝尔森鼠白血病病毒转化的9个scid前B细胞系中的免疫球蛋白重链(Igh)基因重组进行了更详细的分析。我们发现85%的重排Igh等位基因含有大小各异的异常重链多样性(Dh)-重链连接区(Jh)缺失。所有这些缺失都包含Jh元件,并延伸至Igh增强子区域,偶尔还涉及Cμ基因的转换(S)区域。其中一些重排去除了大部分Dh元件,但似乎没有一个延伸至可变重链(Vh)基因。对一个前B细胞系中两个异常重排的Igh等位基因进行的DNA序列分析表明,尽管在没有九聚体(GGTTTTTGT)识别信号序列的情况下存在七聚体样(CACTGTG)识别信号序列,但在重组位点没有保留Dh或Jh编码序列。这些结果表明,失调的重组酶活性可能是阿贝尔森鼠白血病病毒转化的scid前B细胞系中异常Dh-Jh缺失以及Vh-Dh连接缺失的原因。