Witney F R, Furano A V
J Biol Chem. 1984 Aug 25;259(16):10481-92.
We have analyzed the repeated DNA fraction of the rat by characterizing approximately 500 repeat DNA-containing clones using hybridization to a variety of rodent nucleic acids. To facilitate this analysis we devised a method whereby the cloned DNA is transferred to nitrocellulose paper by blotting directly out of colonies of the bacterial clones. In addition to identifying repeated sequences of potential interest (e.g. those transcribed in a tissue-specific manner, or those that are highly conserved in non-rat genomes), we found that, in contrast to what is revealed by the reassociation of rat DNA (e.g. Pearson, W. R., Wu, J. R., and Bonner, J. (1978) Biochemistry 17, 51-59), the rat genome contains a number of different highly repeated (greater than 50,000 copies) sequences. We distinguished the different highly repeated sequences both by their hybridization to different nucleic acids as well as by DNA sequence determination. The highly repeated sequences shared three characteristics that distinguished each of them from the 100,000-member rat satellite I family: (i) they were recovered less often in the cloned repeat DNA library than expected from their copy number in the rat genome; (ii) they reannealed abnormally slowly for their copy number even though they are not significantly divergent; and (iii) they are transcribed in one or more rat tissues. The implications of these findings for the organization of repeated sequences in the rat genome are discussed.
我们通过使用多种啮齿动物核酸进行杂交,对约500个含重复DNA的克隆进行表征,分析了大鼠的重复DNA部分。为便于此分析,我们设计了一种方法,通过直接从细菌克隆菌落中印迹,将克隆的DNA转移到硝酸纤维素纸上。除了鉴定潜在感兴趣的重复序列(例如以组织特异性方式转录的序列,或在非大鼠基因组中高度保守的序列)外,我们发现,与大鼠DNA重缔合所揭示的情况(例如Pearson, W. R., Wu, J. R., and Bonner, J. (1978) Biochemistry 17, 51 - 59)相反,大鼠基因组包含许多不同的高度重复(超过50,000个拷贝)序列。我们通过它们与不同核酸的杂交以及DNA序列测定来区分不同的高度重复序列。这些高度重复序列具有三个特征,将它们与100,000个成员的大鼠卫星I家族区分开来:(i)在克隆的重复DNA文库中,它们的回收频率低于根据其在大鼠基因组中的拷贝数预期的频率;(ii)尽管它们没有明显的差异,但就其拷贝数而言,它们复性异常缓慢;(iii)它们在一种或多种大鼠组织中被转录。本文讨论了这些发现对大鼠基因组中重复序列组织的意义。