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作 者:李玉岭[1] 周厚君[1] 林二培[1] 黄华宏[1] 徐莉莉[1] 童再康[1]
机构地区:[1]浙江农林大学林业与生物技术学院亚热带森林培育国家重点实验室培育基地,临安311300
出 处:《林业科学》2013年第9期52-61,共10页Scientia Silvae Sinicae
基 金:浙江省自然科学基金项目(Y3110453);浙江省农业科技重点项目(2011C12014);浙江省重点创新团队(2009R50035-9);浙江省农业科技重大专项(2008C02004-1);浙江农林大学研究生科研创新基金项目(3122013240218);浙江省重大科技专项(2009C12098)
摘 要:Squamosa promoter binding protein like genes(SPLs)对植物开花具有重要的调控作用。基于转录组序列并利用RACE技术从光皮桦中分离获得BlSPL1基因,其cDNA序列全长1 825 bp,包含开放阅读框长1 170 bp,编码389个氨基酸,与桃PpSPL1(EMJ10405)的同源性最高(67%),属于陆地植物SPLs基因家族的group VII分支。表达分析显示BlSPL1在光皮桦芽、雌花、雄花、幼苗中均有表达,在雄花和幼苗中表达量较低,但在芽发育成雌花过程中明显上调,推测其可能对早期的雌花形成起调控作用。同时,从57个不同的光皮桦无性系中克隆BlSPL1的基因组序列,进行单核苷酸多态性(SNP)分析,共检测到98个SNP位点,SNP频率为1/26 bp,多样性指数π为0.007 12。在外显子区域,共检测到28个SNP位点,其中11个为同义突变,17个为错义突变。进一步的连锁不平衡分析显示,随着序列长度的增加,不同光皮桦群体BlSPL1内的SNPs连锁不平衡在基因内部迅速衰退。Squamosa promoter binding protein like genes(SPLs) play an important role in regulating flowering of plants. In this study, one SPL gene named BISPLI was cloned from Betula luminifera using RACE (rapid-amplification of cDNA ends) strategy. The cDNA of BISPL1 is 1 825 bp in length with an open reading frame (ORF) encoding a protein of 389 aa. The deduced protein sequence of the BISPLI shares the highest identity with PpSPL1 (EMJI0405) (67%) and belongs to group VII of SPL family from land plants. Expression analysis indicated that the BISPL1 transcripts were at a relatively low level in male flower and seedlings, but were apparently up-regulated during the development from buds to female flowers, which implied that BISPL1 might play important roles in early stage of female flower formation. At the same time, the corresponding genomic fragments of BISPL1 were also cloned from 57 different germplasms for the single nucleotide polymorphism (SNP) analysis. A total of 98 SNPs were detected, and the frequency and diversity of SNPs were 1/26 bp and O. 007 12, respectively. There were 28 SNPs detected in the exons of BISPL1, among which, there were 11 synonymous and 17 missense mutations SNPs, respectively. Linkage disequilibrium (LD) analysis showed that I.D declined rapidly within the BISPL1 along with the length increasing in different population of B. luminifera, suggesting that LD mapping based on BlSPL1 gene would be feasible and useful in B. luminifera.
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