Flick K E, McHugh D, Heath J D, Stephens K M, Monnat R J, Stoddard B L
Fred Hutchinson Cancer Research Center, Seattle, Washington 98104, USA.
Protein Sci. 1997 Dec;6(12):2677-80. doi: 10.1002/pro.5560061226.
The homing endonuclease I-PpoI is encoded by an optional third intron, Pp LSU 3, found in nuclear, extrachromosomal copies of the Physarum polycephalum 26S rRNA gene. This endonuclease promotes the lateral transfer or "homing" of its encoding intron by recognizing and cleaving a partially symmetric, 15 bp homing site in 26S rDNA alleles that lack the Pp LSU 3 intron. The open reading frame encoding I-PpoI has been subcloned, and the endonuclease has been overproduced in E. coli. Purified recombinant I-PpoI has been co-crystallized with a 21 bp homing site DNA duplex. The crystals belong to space group P3(1)21, with unit cell dimensions a = b = 114 A, c = 89 A. The results of initial X-ray diffraction experiments indicate that the asymmetric unit contains an enzyme homodimer and one duplex DNA molecule, and that the unit cell has a specific volume of 3.4 A3/dalton. These experiments also provide strong evidence that I-PpoI contains several bound zinc ions as part of its structure.
归巢核酸内切酶I-PpoI由一个可选的第三个内含子Pp LSU 3编码,该内含子存在于多头绒泡菌26S rRNA基因的核内、染色体外拷贝中。这种核酸内切酶通过识别并切割26S rDNA等位基因中一个部分对称的15 bp归巢位点来促进其编码内含子的侧向转移或“归巢”,这些等位基因缺乏Pp LSU 3内含子。编码I-PpoI的开放阅读框已被亚克隆,并且该核酸内切酶已在大肠杆菌中过量表达。纯化的重组I-PpoI已与一个21 bp归巢位点DNA双链体共结晶。晶体属于空间群P3(1)21,晶胞参数a = b = 114 Å,c = 89 Å。初步X射线衍射实验结果表明,不对称单元包含一个酶同二聚体和一个双链DNA分子,并且晶胞的比容为3.4 Å3/道尔顿。这些实验还提供了有力证据,表明I-PpoI在其结构中包含几个结合的锌离子。