Chatterjee A, Faust C J, Molinari-Storey L, Kiochis P, Poustka A, Herman G E
Institute for Molecular Genetics, Baylor College of Medicine, Houston, Texas 77030.
Genomics. 1994 May 1;21(1):49-57. doi: 10.1006/geno.1994.1223.
A yeast artificial chromosome (YAC) contig of approximately 2.3 Mb has been constructed for the region of the mouse X chromosome between Gabra3 and G6pd. YACs were isolated from four genomic libraries by PCR or hybridization screening for the loci Gabra3, DXHX1104, F8a, DXHX52, DXBay2, L1cam, and Rsvp. Orientation of YACs was performed by isolation of ends using several PCR-based methods, including an adaptation for mouse YAC analysis of interspersed repetitive sequence (IRS)-vector PCR. YAC ends were mapped on a panel of somatic cell hybrids, in an interspecific backcross, using pulsed-field gel (PFG) electrophoresis or by hybridization to other YACs in the contig. Overlapping YACs were further aligned by restriction mapping using rare-cutter restriction endonucleases, as well as by comparison of IRS-PCR fingerprints. This contig represents the largest one assembled to date in the mouse. It should facilitate the isolation of genes in the region and may aid in the completion of a physical contig for the homologous human region, Xq28.
已构建了一个约2.3 Mb的酵母人工染色体(YAC)重叠群,覆盖小鼠X染色体上位于Gabra3和G6pd之间的区域。通过PCR或杂交筛选从四个基因组文库中分离出YAC,筛选的位点包括Gabra3、DXHX1104、F8a、DXHX52、DXBay2、L1cam和Rsvp。使用几种基于PCR的方法分离YAC末端来确定YAC的方向,其中包括一种适用于小鼠YAC分析的散布重复序列(IRS)-载体PCR方法。利用脉冲场凝胶(PFG)电泳或通过与重叠群中的其他YAC杂交,将YAC末端定位在一组体细胞杂种上以及种间回交中。使用稀有切割限制内切酶通过限制酶切图谱以及通过比较IRS-PCR指纹图谱,进一步排列重叠的YAC。这个重叠群是目前在小鼠中组装的最大的一个。它应有助于分离该区域的基因,并可能有助于完成同源人类区域Xq28的物理重叠群。