Ogawa A, Solovei I, Hutchison N, Saitoh Y, Ikeda J E, Macgregor H, Mizuno S
Department of Applied Biological Chemistry, Faculty of Agriculture, Tohoku University, Sendai, Japan.
Chromosome Res. 1997 Apr;5(2):93-101. doi: 10.1023/a:1018461906913.
A non-repetitive genomic DNA region of about 25 kb was cloned from the W chromosome of chicken using a genomic library prepared from a single W chromosome of the chicken. This region was mapped by fluorescence in situ hybridization (FISH) with mitotic and lampbrush chromosomes to a position between the major EcoRI family and the pericentromeric Xhol family on the W chromosome. A 0.6-kb EcoRI fragment (EE0.6) subcloned from this region consists of a sequence that can be obtained by the exon-trapping procedure and flanking sequences. Sequences, which are closely similar to that of EE0.6, are widely conserved on the W chromosomes of Carinatae birds, as revealed by Southern blot hybridization to HindIII-digested female and male genomic DNAs from 18 species of birds belonging to eight different taxonomic orders. The female sex of those birds can be determined by the presence of an unambiguous female-specific band. For many species of birds, the female sex can also be determined by polymerase chain reaction (PCR) using a set of primers from the flanking sequences in the chicken EE0.6.
利用从鸡的单条W染色体构建的基因组文库,从鸡的W染色体上克隆出了一个约25 kb的非重复基因组DNA区域。通过用有丝分裂染色体和灯刷染色体进行荧光原位杂交(FISH),将该区域定位到W染色体上主要的EcoRI家族和着丝粒周围的Xhol家族之间的一个位置。从该区域亚克隆的一个0.6 kb的EcoRI片段(EE0.6)由一个可通过外显子捕获程序获得的序列及其侧翼序列组成。通过对来自8个不同分类目的18种鸟类的雌性和雄性基因组DNA进行HindIII酶切后的Southern杂交分析发现,与EE0.6序列高度相似的序列在鸡形目鸟类的W染色体上广泛保守。这些鸟类的雌性性别可通过出现明确的雌性特异性条带确定。对于许多鸟类物种,也可使用一组来自鸡EE0.6侧翼序列的引物,通过聚合酶链反应(PCR)来确定雌性性别。