Drabkin H, Wright M, Jonsen M, Varkony T, Jones C, Sage M, Gold S, Morse H, Mendez M, Erickson P
University of Colorado Medical Center, Denver 80262.
Genomics. 1990 Nov;8(3):435-46. doi: 10.1016/0888-7543(90)90029-t.
A somatic cell hybrid mapping panel and molecular probes have been developed for human chromosome 3. This panel defines 11 regions for the short and long arms of the chromosome. Four hundred thirty-two probes have been mapped using these hybrids. One hundred thirty-one of these probes were derived from EcoRI and HindIII flow-sorted libraries. The remaining 301 probes were isolated from NotI boundary and random (partial MboI) libraries constructed from a hybrid that provided a relative enrichment in 3p DNA sequences. For some regions of the chromosome, significant differences in the distribution of probes were noted. This was observed for both the unique sequence flow-sorted and NotI probes. These differences are in agreement with previous suggestions that Giemsa light bands are GC-rich, and therefore gene-rich (especially housekeeping genes), and that the Giemsa dark bands may contain DNA that is more highly condensed. The isolation of probes from different types of libraries, or by different screening strategies, appears to reduce deficiencies that might arise from the use of probes derived with a more limited approach. These hybrids and probes should facilitate the construction of physical and genetic linkage maps to identify various disease loci involving chromosome 3.
已经开发出用于人类3号染色体的体细胞杂种定位板和分子探针。该定位板确定了该染色体短臂和长臂的11个区域。使用这些杂种对432个探针进行了定位。其中131个探针来自EcoRI和HindIII流式分选文库。其余301个探针是从NotI边界文库和从一个在3p DNA序列中相对富集的杂种构建的随机(部分MboI)文库中分离出来的。对于该染色体的某些区域,注意到探针分布存在显著差异。在独特序列流式分选探针和NotI探针中均观察到了这种差异。这些差异与先前的观点一致,即吉姆萨浅带富含GC,因此富含基因(尤其是管家基因),而吉姆萨深带可能包含凝聚程度更高的DNA。从不同类型的文库中或通过不同的筛选策略分离探针,似乎可以减少因使用方法较为有限而衍生的探针可能出现的缺陷。这些杂种和探针应有助于构建物理和遗传连锁图谱,以识别涉及3号染色体的各种疾病位点。