Tone M, Sakaki Y, Hashiguchi T, Mizuno S
Chromosoma. 1984;89(3):228-37. doi: 10.1007/BF00295004.
Two female-specific repeating DNA units of 0.6 kilobase pairs (kb) and 1.1 kb, produced by digesting the genomic DNA of the White Leghorn chicken with Xho I, were cloned by inserting them into the Xho I site of an Escherichia coli plasmid vector pACYC177. Two such recombinant plasmids, pAGD0601 and pAGD1101, containing a single 0.6-kb and 1.1-kb sequence, respectively, were used as molecular probes. In situ hybridization of the 3H-probes to the metaphase chromosomes from the female White Leghorn embryos revealed their localization in the W chromosome. Semiquantitative Southern blot hybridization with 32P-probes in excess indicated that the 0.6-kb unit and 1.1-kb unit were repeated approximately 14,000 and 6,000 times, respectively, in the W chromosome. The two units comprised about 46% of the W chromosomal DNA. These two repeating units were found in the female genomes of every line of Gallus g. domesticus tested and in the female genomes of three jungle fowl species (G. gallus, G. sonneratii, and G. varius) but not in three species belonging to other genera in the suborder Galli. Hha I sites in the 0.6-kb and 1.1-kb repeating units were shown to be extensively methylated and a significant fraction of the Hpa II sites in the 0.6-kb repeating units were also shown to be methylated in the female genome of the White Leghorn. Methylation patterns of Hpa II sites in or around the 0.6-kb repeating units examined by the Msp I digestion were similar in the various lines of domestic fowls and the two species of jungle fowls, but G varius (black or green jungle fowl) produced a different pattern of digestion with Msp I.
用Xho I酶切白来航鸡基因组DNA产生的两个0.6千碱基对(kb)和1.1 kb的雌性特异性重复DNA单元,通过插入大肠杆菌质粒载体pACYC177的Xho I位点进行克隆。两个这样的重组质粒,pAGD0601和pAGD1101,分别含有单个0.6-kb和1.1-kb序列,用作分子探针。用3H标记的探针与雌性白来航胚胎中期染色体进行原位杂交,结果显示它们定位于W染色体上。用过量的32P标记探针进行的半定量Southern印迹杂交表明,0.6-kb单元和1.1-kb单元在W染色体上分别重复约14,000次和6,000次。这两个单元约占W染色体DNA的46%。在所测试的家鸡(Gallus g. domesticus)各品系的雌性基因组以及三种原鸡(G. gallus、G. sonneratii和G. varius)的雌性基因组中都发现了这两个重复单元,但在鸡亚目其他属的三个物种中未发现。0.6-kb和1.1-kb重复单元中的Hha I位点被证明广泛甲基化,并且在白来航鸡的雌性基因组中,0.6-kb重复单元中的很大一部分Hpa II位点也被证明甲基化。通过Msp I酶切检测的0.6-kb重复单元内部或周围Hpa II位点的甲基化模式,在家鸡各品系和两种原鸡中相似,但G varius(黑原鸡或绿原鸡)用Msp I酶切产生了不同的酶切模式。