Razin S V, Gromova I I
Institute of Gene Biology, Russian Academy of Sciences, Moscow.
Bioessays. 1995 May;17(5):443-50. doi: 10.1002/bies.950170512.
The specificity of eukaryotic DNA organization into loops fixed to the nuclear matrix/chromosomal scaffold has been studied for more than fifteen years. The results and conclusions of different authors remain, however, controversial. Recently, we have elaborated a new approach to the study of chromosomal DNA loops. Instead of characterizing loop basements (nuclear matrix DNA), we have concentrated our efforts on the characterization of individual loops after their excision by DNA topoisomerase II-mediated DNA cleavage at matrix attachment sites. In this review the results of applying this mapping approach are compared with the results and conclusions from studies of nuclear matrix DNA. An attempt is also made to reconsider all data about the specificity of DNA interactions with the nuclear matrix and to suggest a model of spatial organization of the eukaryotic genome which resolves apparent contradictions between these data.
真核生物DNA组织成固定于核基质/染色体支架的环的特异性已经研究了十五年多。然而,不同作者的结果和结论仍存在争议。最近,我们阐述了一种研究染色体DNA环的新方法。我们没有对环的基部(核基质DNA)进行表征,而是将精力集中在通过DNA拓扑异构酶II介导的在基质附着位点的DNA切割切除单个环之后对其进行表征。在这篇综述中,将这种图谱绘制方法的应用结果与核基质DNA研究的结果和结论进行了比较。还尝试重新审视所有关于DNA与核基质相互作用特异性的数据,并提出一个真核生物基因组空间组织模型,该模型解决了这些数据之间明显的矛盾。