CEITEC, Center of Molecular Medicine, Masaryk University, Brno, Czech Republic.
Leuk Res. 2013 Jul;37(7):802-8. doi: 10.1016/j.leukres.2013.03.018. Epub 2013 Apr 20.
The technology of array comparative genomic hybridization (array-CGH/aCGH) enabled the identification of novel genomic aberrations in chronic lymphocytic leukemia (CLL) including the monoallelic and biallelic deletions affecting 22q11 locus. In contrast to previous publications, we hypothesized that the described 22q11 deletions are a consequence of the rearrangement of immunoglobulin lambda light chain locus (IGL) segments surrounding several protein-coding genes located in this region. Indeed, using array-CGH and PCR analysis we show that all deletions (n=7) affecting the 22q11 locus in our cohort (n=40) are based on the physiological mechanism of IGL rearrangement. This demonstrates that this loss of genetic material is likely not pathogenic and in fact is merely a marker of IGL rearrangement.
阵列比较基因组杂交(array-CGH/aCGH)技术使得鉴定慢性淋巴细胞白血病(CLL)中的新型基因组异常成为可能,包括影响 22q11 基因座的单等位基因和双等位基因缺失。与之前的出版物不同,我们假设描述的 22q11 缺失是免疫球蛋白 lambda 轻链基因座(IGL)周围几个位于该区域的蛋白质编码基因的重排的结果。事实上,使用 array-CGH 和 PCR 分析,我们表明我们队列中影响 22q11 基因座的所有缺失(n=7)都基于 IGL 重排的生理机制。这表明这种遗传物质的丢失可能不是致病性的,实际上只是 IGL 重排的标志物。