Supply P, de Kerchove d'Exaerde A, Roganti T, Goffeau A, Foury F
Unité de Biochimie Physiologique, Université Catholique de Louvain, Belgium.
Mol Cell Biol. 1995 Oct;15(10):5389-95. doi: 10.1128/MCB.15.10.5389.
Chimeric PMA1::PMA2 sequences, placed under the control of the PMA1 promoter, were constructed by in vivo recombination between a gapped linearized plasmid containing the PMA2 gene and four different fragments of the PMA1 gene. Correct in-frame assembly of the PMA sequences was screened by the expression of the lacZ reporter gene fused to the PMA2 coding region. Restriction and sequencing analysis of 35 chimeras showed that in all cases, the hybrid sequences was obtained as fusions between continuous sequences specific to PMA1 and PMA2, separated by a region of identity. In all but three cases, the junction sequences were not located at regions of greatest identity. Strikingly, depending on the PMA1 fragment used, junction distribution fell into two categories. In the first, the junctions were scattered over several hundreds of nucleotides upstream of the extremity of the PMA1 fragment, while in the second, they were concentrated at this extremity. Analysis of the alignment of the PMA1 and PMA2 sequences suggests that the distribution is not related to the size of the region of identity at the PMA1-PMA2 boundary but depends on the degree of identity of the PMA genes upstream of the region of identity, the accumulation of successive mismatches leading to a clustered distribution of the junctions. Moreover, the introduction of seven closely spaced mismatches near the end of a PMA1 segment with an otherwise-high level of identity with PMA2 led to a significantly increased concentration of the junctions near this end. These data show that a low level of identity in the vicinity of the common boundary stretch is a strong barrier to recombination. In contrast, consecutive mismatches or regions of overall moderate identity which are located several hundreds of nucleotides upstream from the PMA1 end do not necessarily block recombination.
通过在含有PMA2基因的缺口线性化质粒与PMA1基因的四个不同片段之间进行体内重组,构建了置于PMA1启动子控制下的嵌合PMA1::PMA2序列。通过与PMA2编码区融合的lacZ报告基因的表达筛选PMA序列的正确读框组装。对35个嵌合体的限制性酶切和测序分析表明,在所有情况下,杂交序列都是作为PMA1和PMA2特异的连续序列之间的融合体获得的,中间由一个同源区域隔开。除了三个案例外,连接序列并不位于同源性最高的区域。引人注目的是,根据所使用的PMA1片段,连接点分布分为两类。在第一类中,连接点分散在PMA1片段末端上游数百个核苷酸处,而在第二类中,它们集中在该末端。对PMA1和PMA2序列比对的分析表明,这种分布与PMA1-PMA2边界处同源区域的大小无关,而是取决于同源区域上游PMA基因的同源程度,连续错配的积累导致连接点的聚集分布。此外,在与PMA2具有较高同源性的PMA1片段末端附近引入七个紧密间隔的错配,导致该末端附近连接点的浓度显著增加。这些数据表明,共同边界延伸附近的低同源性是重组的强大障碍。相比之下,位于PMA1末端上游数百个核苷酸处的连续错配或整体中等同源性区域不一定会阻止重组。