Debuchy R, Purton S, Rochaix J D
Department of Molecular Biology, University of Geneva, Switzerland.
EMBO J. 1989 Oct;8(10):2803-9. doi: 10.1002/j.1460-2075.1989.tb08426.x.
The argininosuccinate lyase (ASL) gene of Chlamydomonas reinhardtii has been cloned using four oligonucleotide probes corresponding to highly conserved regions of the ASL polypeptide sequence. The identity of the gene was confirmed by partial sequencing. It is unique, contains several introns and spans a region less than 7.8 kb that includes highly repetitive sequences. Using a particle gun, a reliable nuclear transformation system has been established by complementing three mutants deficient in ASL activity with the wild-type ASL gene. Analysis of the transformants reveals variable patterns of integration of the transforming DNA into the nuclear genome. Previous work has mapped the mutations in the mutants arg2 and arg7 to either end of the ARG7 locus 1.0 to 1.6 recombination map units apart. Our transformation results show that these two mutations are located within a region of 7.8 kb. This allows for the first correlation of the recombination map and the molecular map at the ARG7 locus and indicates a high recombination frequency in this region of the nuclear genome.
利用与精氨琥珀酸裂解酶(ASL)多肽序列高度保守区域相对应的4种寡核苷酸探针,克隆了莱茵衣藻的精氨琥珀酸裂解酶(ASL)基因。通过部分测序确认了该基因的身份。它是唯一的,含有几个内含子,跨度小于7.8 kb的区域,包括高度重复序列。利用粒子枪,通过用野生型ASL基因互补3个ASL活性缺陷型突变体,建立了可靠的核转化系统。对转化体的分析揭示了转化DNA整合到核基因组中的可变模式。先前的工作已将突变体arg2和arg7中的突变定位到ARG7基因座两端,相距1.0至1.6个重组图距单位。我们的转化结果表明,这两个突变位于7.8 kb的区域内。这使得首次能够将ARG7基因座处的重组图谱与分子图谱相关联,并表明该核基因组区域具有高重组频率。