Jabs E W, Wolf S F, Migeon B R
Somat Cell Mol Genet. 1984 Jan;10(1):93-103. doi: 10.1007/BF01534476.
Recombinants containing human repetitive DNA sequences were identified by dot hybridization and classified with respect to presence on the X chromosome and homology to mouse DNA. Using genomic probes that differ in number of X chromosomes, we observed extensive homology between human autosomal and X sequences. Hybridization to genomic probes that differ in species of origin indicate that these reiterated sequences have diverged between mouse and man. Eleven recombinants, each containing a different reiterated sequence(s), were hybridized in situ to metaphase chromosomes of mouse and man. These studies indicate that reiterated DNA which is homologous to the human X chromosome is more similar to DNA of human autosomes than to any murine chromosome. Therefore, it seems that reiterated DNA sequences on the human X chromosome have diverged as much during mammalian evolution as sequences on human autosomes. Moreover, the extensive modification of the original mammalian X has not interferred with the X inactivation process.
通过点杂交鉴定出含有人类重复DNA序列的重组体,并根据其在X染色体上的存在情况以及与小鼠DNA的同源性进行分类。使用X染色体数量不同的基因组探针,我们观察到人类常染色体和X染色体序列之间存在广泛的同源性。与起源物种不同的基因组探针杂交表明,这些重复序列在小鼠和人类之间已经发生了分化。11个重组体,每个都包含不同的重复序列,与小鼠和人类中期染色体进行原位杂交。这些研究表明,与人类X染色体同源的重复DNA与人类常染色体的DNA比与任何小鼠染色体的DNA更相似。因此,似乎人类X染色体上的重复DNA序列在哺乳动物进化过程中与人类常染色体上的序列一样发生了很大的分化。此外,原始哺乳动物X染色体的广泛修饰并未干扰X染色体失活过程。