Gerard R D, Montelone B A, Walter C F, Innis J W, Scott W A
Mol Cell Biol. 1985 Jan;5(1):52-8. doi: 10.1128/mcb.5.1.52-58.1985.
A nuclease-sensitive region forms in chromatin containing a 273-base-pair (bp) segment of simian virus 40 DNA encompassing the viral origin of replication and early and late promoters. We have saturated this region with short deletion mutations and compared the nuclease sensitivity of each mutated segment to that of an unaltered segment elsewhere in the partially duplicated mutant. Although no single DNA segment is required for the formation of a nuclease-sensitive region, a deletion mutation (dl45) which disrupted both exact copies of the 21-bp repeats substantially reduced nuclease sensitivity. Deletion mutations limited to only one copy of the 21-bp repeats had little, if any, effect. A mutant (dl135) lacking all copies of the 21- and 72-bp repeats, while retaining the origin of replication and the TATA box, did not exhibit a nuclease-sensitive region. Mutants which showed reduced nuclease sensitivity had this effect throughout the nuclease-sensitive region, not just at the site of the deletion, indicating that although multiple determinants must be responsible for the nuclease-sensitive chromatin structure they do not function with complete independence. Mutant dl9, which lacks the late portion of the 72-bp segment, showed reduced accessibility to BglI, even though the BglI site is 146 bp away from the site of the deletion.
在染色质中形成了一个核酸酶敏感区域,该区域包含猿猴病毒40(SV40)DNA的一段273个碱基对(bp)的片段,其涵盖病毒复制起点以及早期和晚期启动子。我们用短缺失突变使该区域饱和,并将每个突变片段的核酸酶敏感性与部分重复突变体中其他未改变片段的核酸酶敏感性进行比较。尽管形成核酸酶敏感区域不需要单一的DNA片段,但一个破坏了21 bp重复序列两个精确拷贝的缺失突变(dl45)显著降低了核酸酶敏感性。仅限于21 bp重复序列一个拷贝的缺失突变几乎没有影响。一个缺失所有21 bp和72 bp重复序列拷贝但保留复制起点和TATA框的突变体(dl135)未表现出核酸酶敏感区域。核酸酶敏感性降低的突变体在整个核酸酶敏感区域都有这种效应,而不仅仅是在缺失位点,这表明尽管多个决定因素必定对核酸酶敏感的染色质结构起作用,但它们并非完全独立发挥功能。缺失72 bp片段后期部分的突变体dl9对BglI的可及性降低,尽管BglI位点距离缺失位点有146 bp。