鱼腥藻PCC7120基因组中一个影响异形胞发育和图式形成的新区域
A NOVEL REGION INVOLVED IN HETEROCYST DEVELOPMENT AND PATTERN FORMATION IN THE GENOME OFANABAENA SP. PCC 7120
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摘要: 以Tn5-1087b诱变鱼腥藻PCC7120,筛选不能利用氮气生长、异形胞图式发生变化的突变株.突变株#1801经缺氮诱导24h后无异形胞形成,48h后沿藻丝形成少量成熟异形胞,占藻细胞总数比例为2.8%,其异形胞发育速度和形成频率均与野生型有显著区别.以ClaⅠ酶切该突变株总DNA、自环化后以电泳冲法转化大肠杆菌,回收带有插入位点两侧DNA片段的转座子Tn5-1087b.经测序确定转座子位于未知功能基因alr0099第148和149碱基之间.为证明突变性状确由alr0099内的插入突变引起而不是由于其他二次突变,通过同源双交换将含新霉素抗性基因的C.K2片段定向插入基因组中alr0099的EcoRV位点,获得重构的鱼腥藻突变株DR214,其表型与原突变株#1801相同.以上结果表明alr0099或其下游基因是鱼腥藻PCC7120基因组中与异形胞发育和图式形成相关的一个新区域.Abstract: Anabaena sp. PCC 7120 was mutagenized with trans poson Tn5-1087b and screened for mutants unable to grow on dinitrogen and alter ed in heterocyst pattern. Mutant #1801 forms no visible heterocyst within 24h after nitrogen stepdown, and a small number of mature heterocysts within 48h, which a mount to 2.8% of total cell number. The mutant is significantly different from the wild type in rate and frequency of heterocyst differentiation. The flanking g enomic DNA and the transposon were retrieved from the mutant by restriction of i ts total DNA with ClaI, recircularization and electroporation intoE.coli.A s shown with sequencing, the transposon was inserted between Nt. 148 and 149 of alr0099, a gene of unknown function. To prove that the phenotype of the muta nt was indeed due to the insertion withinalr0099 but not a secondary mutati on, we inserted C. K2 cassette, a neomycin resistance marker, into the cyanobact erial genome at the EcoRV site ofalr0099 via double h omologous recombinatio ns. The reconstructed mutant DR214 showed the same phenotype as #1801. These res ults indicate thatalr0099 or its downstream genes sta nd for a novel region involved in heterocyst development and pattern formation in the genome ofAnab aena sp. PCC 7120.