Obe G, Kamra O P
Mutat Res. 1986 May;174(1):35-46. doi: 10.1016/0165-7992(86)90074-6.
The frequencies of chromosomal aberrations induced by the restriction endonuclease Alu I (recognition site AG/CT) can be elevated to a similar extent by additional treatments with a single-strand-specific endonuclease from Neurospora crassa (EC 3.1.30.1), or with ammonium sulfate in which the Neurospora endonuclease is suspended. These data indicate that Alu I does not produce DNA single-strand breaks in the chromatin of living cells, which can be recognized by the Neurospora endonuclease. The salt may induce conformational changes in the chromatin which make more recognition sites available for Alu I. Experiments with recovery times between the treatments with Alu I and the salt indicate that Alu I can act in the nucleus for at least 40 min.
限制性内切酶Alu I(识别位点AG/CT)诱导的染色体畸变频率,可通过用来自粗糙脉孢菌的单链特异性内切酶(EC 3.1.30.1)或用悬浮有粗糙脉孢菌内切酶的硫酸铵进行额外处理,提高到类似程度。这些数据表明,Alu I在活细胞染色质中不会产生可被粗糙脉孢菌内切酶识别的DNA单链断裂。盐可能诱导染色质构象变化,使更多识别位点可被Alu I利用。对Alu I和盐处理之间恢复时间的实验表明,Alu I可在细胞核中作用至少40分钟。