Strick R, Laemmli U K
Department of Biochemistry, University of Geneva, Switzerland.
Cell. 1995 Dec 29;83(7):1137-48. doi: 10.1016/0092-8674(95)90140-x.
SARs are candidate DNA elements for defining the bases of chromatin loops and possibly for serving as cis elements of chromosome dynamics. SARs contain numerous A tracts, whose altered DNA structure is recognized by cooperatively interacting proteins such as topoisomerase II. We constructed multi-AT hook (MATH) proteins and demonstrate that they specifically bind the clustered A tracts of SARs in chromatin and chromosomes. They are also potent inhibitors of chromosome assembly in mitotic Xenopus extracts, demonstrating the importance of SARs in this process. Titration of SARs with MATH20 (20 hooks) blocks shape determination of chromatids but not chromatin condensation per se. SARs are also required for shape maintenance of chromosomes. If MATH20 is added after formation of chromatids, they collapse and are reshaped by an active, mitotic process into spherical chromatid balls.
支架附着区域(SARs)是用于定义染色质环基础以及可能作为染色体动力学顺式元件的候选DNA元件。SARs含有大量富含A的序列(A tracts),其改变的DNA结构可被诸如拓扑异构酶II等协同相互作用的蛋白质识别。我们构建了多AT钩(MATH)蛋白,并证明它们能特异性结合染色质和染色体中SARs的成簇富含A的序列。它们也是有丝分裂非洲爪蟾提取物中染色体组装的有效抑制剂,证明了SARs在此过程中的重要性。用MATH20(20个钩)滴定SARs会阻止染色单体的形态确定,但不会阻止染色质本身的凝聚。染色体的形态维持也需要SARs。如果在染色单体形成后加入MATH20,它们会坍塌,并通过一个活跃的有丝分裂过程重新塑造为球形染色单体球。