Htun H, Lund E, Westin G, Pettersson U, Dahlberg J E
EMBO J. 1985 Jul;4(7):1839-45. doi: 10.1002/j.1460-2075.1985.tb03858.x.
We show here that human U2 small nuclear RNA genes contain a 'strong nuclease S1 cleavage site' (SNS1 site), a sequence that is very sensitive to digestion by nuclease S1. This site is located 0.50-0.65 kb downstream of the U2 RNA coding region. It comprises a 0.15-kb region in which (dC-dT)n:(dA-dG)n co-polymeric stretches represent greater than 90% of the sequence. Nuclease S1 is able to excise unit length repeats of the human U2 RNA genes both from cloned fragments and total human genomic DNA. The precise locations of the cleavage sites are dependent on the superhelicity of the substrate DNA. In negatively supercoiled substrates, cleavages are distributed over the entire 0.15-kb region, but in linearized substrates, they occur within a more limited region, mainly at the boundary of the SNS1 site closest to the human U2 RNA coding region. Nuclease S1 cleavage of negatively supercoiled substrates occurs at pHs as high as 7.0; in contrast, cleavage of linearized substrates requires a pH less than 5.0, indicating that supercoiling contributes to the sensitivity of this site. Mung bean nuclease gives results similar to that observed with nuclease S1.
我们在此表明,人类U2小核RNA基因包含一个“强核酸酶S1切割位点”(SNS1位点),该序列对核酸酶S1的消化非常敏感。此位点位于U2 RNA编码区域下游0.50 - 0.65 kb处。它由一个0.15 kb的区域组成,其中(dC - dT)n:(dA - dG)n共聚物片段占该序列的90%以上。核酸酶S1能够从克隆片段和人类基因组总DNA中切除人类U2 RNA基因的单位长度重复序列。切割位点的精确位置取决于底物DNA的超螺旋状态。在负超螺旋底物中,切割分布在整个0.15 kb区域,但在线性化底物中,切割发生在更有限的区域内,主要在最接近人类U2 RNA编码区域的SNS1位点边界处。负超螺旋底物的核酸酶S1切割在pH高达7.0时发生;相比之下,线性化底物的切割需要pH小于5.0,这表明超螺旋增加了该位点的敏感性。绿豆核酸酶给出的结果与核酸酶S1观察到的结果相似。