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4号染色体中部的显微切割与微克隆:41个显微切割克隆的基因定位

Microdissection and microcloning of mid-chromosome 4: genetic mapping of 41 microdissection clones.

作者信息

Bahary N, McGraw D E, Shilling R, Friedman J M

机构信息

Laboratory of Molecular Genetics, Rockefeller University, New York, New York 10021.

出版信息

Genomics. 1993 Apr;16(1):113-22. doi: 10.1006/geno.1993.1148.

Abstract

Available genetic information places the mouse db gene approximately 5 cM distal to Ifa on mid/distal mouse chromosome 4. These data have indicated that there is a relevant paucity of genetic markers that map to this region of chromosome 4. To increase the density of the genetic map on mid-chromosome 4, we have applied the techniques of microdissection and microcloning of the mid-portion of mouse chromosome 4. A total of 47 RFLPs from the microdissection library were used to type the progeny of three C57BL/6J Mus spretus backcrosses. The resulting composite genetic map positions seven known genes, 41 microclones, and three other anonymous markers to a region of approximately 21 cM on mid-chromosome 4 extending from b to Lck. The density of markers in this region of chromosome 4 should be sufficient to initiate the physical mapping of this subchromosomal segment, facilitating efforts to clone the db gene, as well as other uncloned mutant loci in this region of chromosome 4.

摘要

现有的遗传信息表明,小鼠的db基因位于小鼠第4号染色体中部/远端Ifa基因大约5厘摩远的位置。这些数据表明,定位到第4号染色体该区域的遗传标记相当匮乏。为了增加第4号染色体中部的遗传图谱密度,我们应用了小鼠第4号染色体中部的显微切割和微克隆技术。从显微切割文库中总共选取了47个限制性片段长度多态性(RFLP)来对三个C57BL/6J×小家鼠回交后代进行分型。由此得到的复合遗传图谱将7个已知基因、41个微克隆以及其他3个无名标记定位到了第4号染色体中部从b到Lck的大约21厘摩的区域。第4号染色体该区域的标记密度应该足以启动该亚染色体片段的物理图谱构建工作,有助于克隆db基因以及第4号染色体该区域的其他未克隆的突变位点。

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