Fairman J, Chumakov I, Chinault A C, Nowell P C, Nagarajan L
Department of Hematology, University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.
Proc Natl Acad Sci U S A. 1995 Aug 1;92(16):7406-10. doi: 10.1073/pnas.92.16.7406.
Acquired interstitial loss of all or part of the long arm of human chromosome 5 (5q-) is an anomaly that is seen frequently in patients with preleukemic myelodysplasia and acute myelogenous leukemia. Loss of a critical region of overlap at band 5q31.1 in all of these cases, with various cytogenetic breaks, signifies the existence of a key negative regulator of leukemogenesis. Previous studies have defined the proximal and distal ends of the critical region to reside between the genes for IL9 and EGR1, respectively. In this report, we describe a yeast artificial chromosome contig spanning this myeloid tumor suppressor locus. The combined order of the polymorphic loci is centromere-IL9-(D5S525-D5S558-D5S89-D5S526 -D5S393)-D5S399-D5S396-D5S414-EGR1 and telomere. The physical distance between the IL9 and EGR1 genes is estimated to be < 2.4 Mb. Here we report the utility of these polymorphic loci by detecting a submicroscopic deletion of 5q31; an acute myelogenous leukemia patient with a three-way translocation, t(5;18;17)(q31;p11;q11), as the sole anomaly revealed allele loss of the D5S399 and D5S396 loci.
人类5号染色体长臂全部或部分的后天性间质缺失(5q-)是一种在白血病前期骨髓发育异常和急性髓性白血病患者中常见的异常现象。在所有这些病例中,5q31.1带的关键重叠区域缺失,伴有各种细胞遗传学断裂,这表明存在白血病发生的关键负调控因子。先前的研究已确定关键区域的近端和远端分别位于IL9和EGR1基因之间。在本报告中,我们描述了一个跨越该髓系肿瘤抑制基因座的酵母人工染色体重叠群。多态性位点的联合顺序是着丝粒-IL9-(D5S525-D5S558-D5S89-D5S526 -D5S393)-D5S399-D5S396-D5S414-EGR1和端粒。IL9和EGR1基因之间的物理距离估计小于2.4 Mb。在此我们通过检测5q31的亚显微缺失报告这些多态性位点的效用;一名患有三向易位t(5;18;17)(q31;p11;q11)的急性髓性白血病患者,作为唯一异常显示D5S399和D5S396位点的等位基因缺失。