Q型烟粉虱扬州种群cyp6cm1基因内含子抗性相关多态性检测及其5′侧翼序列克隆
Detection of single-nucleotide polymorphisms (SNPs) associated with resistance to neonicotinoid insecticides in the intron of cyp6cm1 gene and cloning of its 5′ flanking sequence in a Q-biotypeBemisia tabaci population from Yangzhou
袁林泽1, 2** 王少丽3 王文龙2 杜予州2 张友军3 王建军2***
点击：1914次 下载：27次
DOI：10.7679/j.issn.2095-1353.2015.005
作者单位：1. 扬州市邗江区植物保护站，扬州 225009；2. 扬州大学园艺与植物保护学院，扬州225009； 3. 中国农业科学院蔬菜花卉研究所，北京 100081
中文关键词：烟粉虱，细胞色素P450，内含子，基因组步移
英文关键词：Bemisia tabaci, cytochrome P450, intron, genome walking
中文摘要：【目的】 烟粉虱Bemisia tabaci（Gennadius）已对包括有机磷类、拟除虫菊酯类、新烟碱类和昆虫生长调节剂等多种杀虫剂产生了不同程度的抗药性，其中尤以对新烟碱类杀虫剂的抗性问题最为突出。本研究旨在克隆Q型烟粉虱扬州种群细胞色素P450基因cyp6cm1片段序列及其5′侧翼序列。【方法】 分别应用PCR和基因组步移技术克隆cyp6cm1基因片段序列及其5′侧翼序列。【结果】 cyp6cm1基因片段序列包括63 bp的外显子片段和826~829 bp的内含子片段。多重序列比对发现，在内含子第195、230和242等3个碱基处存在与新烟碱类杀虫剂抗性相关的单核苷酸多态性（SNPs）。进一步利用基因组步移技术获得了长度为962 bp的cyp6cm1基因5′侧翼序列，利用NNPP在线分析软件预测转录起始位点为位于起始密码子上游57 bp处的碱基A；ConSite软件分析发现，cyp6cm1基因5′侧翼序列具有XRE-AhR、CREB、Oct-1和Broad-complex-4等多种转录因子结合位点。
英文摘要：
[Objectives] The whitefly, Bemisia
tabaci, has developed resistance to a wide range of insecticides, including
organophosphates, pyrethroids, insect growth regulators, and especially
neonicotinoids. To understand the molecular mechanisms underlying neonicotinoid
resistance, the genomic DNA fragment of the cytochrome P450 gene cyp6cm1 and its 5′ flanking sequence were cloned in Q-biotype B. tabaci fromYangzhou. [Methods] PCR and genome walking were used to isolate
the genomic DNA fragment of the cyp6cm1 gene and its flanking sequence. [Results] The genomic fragment of the cyp6cm1 gene contained the last 63 bp of the first exon of the cyp6cm1 gene together with the first 826-829 bp of the adjacent intron. Three
single-nucleotide polymorphisms (SNPs) associated with resistance to
neonicotinoid insecticides were identified by multiple sequences alignment, these
were located at positions 195, 230 and 242 of the intron, respectively. In
addition, the 962 bp 5′ flanking
sequence of cyp6cm1 gene of Q-biotype B. tabaci was cloned by genome walking. NNPP online analysis software predicted the transcription
initiation site as the nucleotide A, which is located 57 bp upstream of the
initiation codon. ConSite software predicted several transcription factor
binding sites in this region, including XRE-AhR, CREB,
Oct-1 and Broad-complex-4.