Blennow E, Telenius H, Larsson C, de Vos D, Bajalica S, Ponder B A, Nordenskjöld M
Department of Clinical Genetics, Karolinska Institute, Stockholm, Sweden.
Hum Genet. 1992 Dec;90(4):371-4. doi: 10.1007/BF00220461.
Marker chromosome are small supernumerary chromosomes that are sometimes associated with developmental abnormalities. Hence, the genes involved in such cases provide an interesting approach to understanding developmental abnormalities in man. As a first step towards isolating such sequences, marker chromosomes need complete characterization. By combining chromosome isolation by flow sorting and the "degenerate oligonucleotide primed - polymerase chain reaction", we have constructed a DNA library specific for a marker chromosome found in a child with severe developmental abnormalities. We used fluorescent in situ hybridization of the library onto normal metaphase spreads ("reverse chromosome painting") and were thus able to determine that the marker consists of the centromeric part of chromosome 7, the telomeric region of the long arm of chromosome 5 and the telomeric region of the short arm of the X-chromosome. Subsequently, we hybridized normal chromosome-specific libraries of the relevant chromosomes onto metaphases containing the marker chromosome ("forward chromosome painting") and could in this manner establish the precise location of the different chromosome regions on the marker chromosome itself. This is a general approach suitable for outlining marker chromosomes in detail, and will aid the identification of the genes involved.
标记染色体是小型额外染色体,有时与发育异常相关。因此,此类病例中涉及的基因提供了一种了解人类发育异常的有趣方法。作为分离此类序列的第一步,标记染色体需要完整的特征描述。通过结合流式细胞分选法进行染色体分离和“简并寡核苷酸引物 - 聚合酶链反应”,我们构建了一个针对在一名患有严重发育异常的儿童中发现的标记染色体的DNA文库。我们将该文库与正常中期染色体铺展物进行荧光原位杂交(“反向染色体涂染”),从而能够确定该标记由7号染色体的着丝粒部分、5号染色体长臂的端粒区域和X染色体短臂的端粒区域组成。随后,我们将相关染色体的正常染色体特异性文库与含有标记染色体的中期染色体进行杂交(“正向染色体涂染”),并以此方式确定不同染色体区域在标记染色体自身上的精确位置。这是一种适用于详细勾勒标记染色体的通用方法,将有助于识别其中涉及的基因。