Donev R M
Institute of Molecular Biology, Bulgarian Academy of Sciences, Sofia.
Mol Cell Biochem. 2000 Nov;214(1-2):103-10. doi: 10.1023/a:1007159421204.
A large variety of DNA sequences have been described in nuclear matrix attachment regions. It could be most likely a result of the different methods used for their isolation. The idea about how different types of known DNA sequences (strongly attached to the nuclear matrix, weakly attached, or not attached) directly participate in anchoring DNA loops to the nuclear matrices isolated by different experimental procedures was tested in this study. Matrix-attached (M) and matrix-independent or loop (L) fractions as well as nuclear matrices were isolated using extractions of nuclei with 25 mM lithium 3,5-diiodosalicylate (LIS), 2 M NaCl, 0.65 M ammonium sulphate containing buffers followed by DNase I/RNase A digestion, or according to so designated conventional method. Using PCR-based and in vitro binding assays it was established that LIS and ammonium sulphate extractions gave similar results for the type of attachment of sequences investigated. The harsh extraction with 2 M NaCl or the conventional procedure led to some rearrangements in the attachment of DNA loops. As a result a big part of matrix attached sequences were found detached in the loop fractions. However, the in vitro binding abilities of the MARs to the nuclear matrices isolated by different methods did not change.
在核基质附着区域已描述了各种各样的DNA序列。这很可能是由于用于分离它们的方法不同所致。本研究测试了关于不同类型的已知DNA序列(与核基质紧密附着、弱附着或未附着)如何直接参与将DNA环锚定到通过不同实验程序分离的核基质上的想法。使用含25 mM 3,5 - 二碘水杨酸锂(LIS)、2 M NaCl、0.65 M硫酸铵的缓冲液对细胞核进行提取,随后进行DNase I/RNase A消化,或者按照所谓的常规方法,分离出基质附着(M)和基质非依赖或环(L)组分以及核基质。通过基于PCR的和体外结合试验确定,对于所研究序列的附着类型,LIS和硫酸铵提取得到了相似的结果。用2 M NaCl进行的严苛提取或常规程序导致DNA环附着发生了一些重排。结果发现,很大一部分与基质附着的序列在环组分中被分离出来。然而,MARs与通过不同方法分离的核基质的体外结合能力并未改变。