Porta G, MacMillan S, Nagaraja R, Mumm S, Zucchi I, Pilia G, Maio S, Featherstone T, Schlessinger D
Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Genome Res. 1997 Jan;7(1):27-36. doi: 10.1101/gr.7.1.27.
Sequence-tagged site (STS) content mapping in yeast artificial chromosomes (YACs) was used to cover the region deleted in two patients affected with X-linked lymphoproliferative disorder. The order of markers includes, centromere to telomere, DXS8009-DXS1206-DXS8078-DXS8044-DXS982- DXS6811-DXS8093-AFM240xblO- DXS75-DXS737-DXS100-DXS6-DXS1046-DXS803 8. The order of six major markers is confirmed by fluorescent in situ hybridization, and all the markers assigned by linkage mapping fall within a 1.6-cM interval. The contig comprises 90 clones containing 89 STSs, yielding a resolution of 50 kb; DNA in a gap just telomeric to DXS8044 has not been found in > 20 equivalents of YACs or bacterial clones. The two deletions were found to have centromeric breakpoints that lie close to DXS1206 and may be identical; the telomeric breakpoints are -150 kb apart, one falling between DXS737 and DXS100, the other between DXS100 and DXS1046. Several STSs near the breakpoints show weak amplification from more than one site; one gives products from three groups of YACs, and lie, respectively, within 50 kb of the centromeric and the two telomeric deletion borders. Such partially duplicated segments of DNA are candidates for involvement in the formation of the deletions.
利用酵母人工染色体(YAC)中的序列标签位点(STS)内容图谱来覆盖两名患有X连锁淋巴增殖性疾病患者中缺失的区域。标记顺序从着丝粒到端粒依次为:DXS8009 - DXS1206 - DXS8078 - DXS8044 - DXS982 - DXS6811 - DXS8093 - AFM240xbl0 - DXS75 - DXS737 - DXS100 - DXS6 - DXS1046 - DXS8038。六个主要标记的顺序通过荧光原位杂交得以确认,并且通过连锁图谱定位的所有标记都落在1.6厘摩的区间内。该重叠群包含90个克隆,含有89个STS,分辨率为50 kb;在超过20倍量的YAC或细菌克隆中均未发现位于DXS8044端粒方向缺口处的DNA。发现这两个缺失的着丝粒断点靠近DXS1206,且可能相同;端粒断点相距约150 kb,一个落在DXS737和DXS100之间,另一个落在DXS100和DXS1046之间。断点附近的几个STS在多个位点显示出微弱扩增;其中一个从三组YAC中产生产物,分别位于着丝粒缺失边界和两个端粒缺失边界的50 kb范围内。这种部分重复的DNA片段可能参与了缺失的形成。