Duffy M, Chambers A
Department of Genetics, University of Nottingham, Queen's Medical Centre, UK.
Nucleic Acids Res. 1996 Apr 15;24(8):1412-9. doi: 10.1093/nar/24.8.1412.
Gel retardation assays using a probe containing the repeat region of a Schizosaccharomyces pombe chromosomal telomere identified four specific DNA- protein complexes in S. pombe total protein extracts (I, I', IIa and IIb). The proteins responsible for these complexes bound to the telomeric repeat region irrespective of whether or not the repeats were in close proximity to the end of a DNA molecule, and none of them bound strongly to single-stranded DNA. The protein responsible for complex I (TeRF I) was separated from the activity responsible for complexes IIa and IIb (TeRF II) using heparin-Sepharose chromatography. Both factors were efficiently cross-competed by an oligonucleotide containing the 18 bp sequence 5'-GGTTACAGGTTACAGGTT-3', which corresponds to two complete telomeric repeat units. Mutation of the T residues at positions 4 and 11 in the oligonucleotide dramatically reduced binding by TeRF II, but had no affect on binding by TeRF I. The protein responsible for complex I' did not bind strongly to either the wild-type or mutant oligonucleotide.
使用含有粟酒裂殖酵母染色体端粒重复区域的探针进行凝胶阻滞分析,在粟酒裂殖酵母总蛋白提取物中鉴定出四种特异性DNA-蛋白质复合物(I、I'、IIa和IIb)。负责这些复合物的蛋白质与端粒重复区域结合,无论这些重复序列是否紧邻DNA分子末端,并且它们都不与单链DNA强烈结合。使用肝素-琼脂糖层析将负责复合物I的蛋白质(端粒重复结合因子I,TeRF I)与负责复合物IIa和IIb的活性(端粒重复结合因子II,TeRF II)分离。这两种因子都能被含有18 bp序列5'-GGTTACAGGTTACAGGTT-3'的寡核苷酸有效交叉竞争,该序列对应于两个完整的端粒重复单元。寡核苷酸中第4位和第11位的T残基发生突变,显著降低了TeRF II的结合,但对TeRF I的结合没有影响。负责复合物I'的蛋白质与野生型或突变型寡核苷酸都没有强烈结合。