中国农业科学 ›› 2021, Vol. 54 ›› Issue (14): 3029-3042.doi: 10.3864/j.issn.0578-1752.2021.14.009

• 植物保护 • 上一篇    下一篇

fl(2)d单等位基因的敲除显著降低小菜蛾的生殖力和育性

李飞飞(),王贝贝,赖颖芳,杨菲颖,尤民生(),何玮毅()   

  1. 闽台作物有害生物生态防控国家重点实验室/福建农林大学应用生态研究所/福建农林大学教育部害虫生态防控国际合作联合实验室/福建农林大学农业农村部闽台作物有害生物综合治理重点实验室/海峡两岸特色作物安全生产省部共建协同创新中心,福州350002
  • 收稿日期:2020-11-06 接受日期:2021-01-15 出版日期:2021-07-16 发布日期:2021-07-26
  • 通讯作者: 尤民生,何玮毅
  • 作者简介:李飞飞,E-mail: lff0371@163.com
  • 基金资助:
    国家重点研发计划(2017YFD0200400);福建省自然科学基金(2019J21369);福建省科技重大专项(2018NZ0002)

Knockout of Single Allele of fl(2)d Significantly Decreases the Fecundity and Fertility inPlutella xylostella

LI FeiFei(),WANG BeiBei,LAI YingFang,YANG FeiYing,YOU MinSheng(),HE WeiYi()   

  1. State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops/Institute of Applied Ecology, Fujian Agriculture and Forestry/International Joint Research Laboratory of Ecological Pest Control, Ministry of Education, Fujian Agriculture and Forestry University/Key Laboratory of Integrated Pest Management for Fujian-Taiwan Crops, Ministry of Agriculture and Rural Affairs, Fujian Agriculture and Forestry/Ministerial and Provincial Joint Innovation Centre for Safety Production of Cross-Strait Crops, Fuzhou 350002
  • Received:2020-11-06 Accepted:2021-01-15 Online:2021-07-16 Published:2021-07-26
  • Contact: MinSheng YOU,WeiYi HE

摘要:

【目的】RNA甲基化是基因转录后水平表观修饰的主要形式,参与了众多重要的细胞学过程。小菜蛾(Plutella xylostella)是危害十字花科蔬菜的重要寡食性害虫,与RNA甲基化相关基因的功能尚未见报道。本研究通过克隆小菜蛾的RNA甲基化蛋白同源基因fl(2)d,鉴定其表达模式,并敲除该基因以探究其生物学功能。【方法】通过小菜蛾基因组网站查找fl(2)d基因序列,PCR扩增其蛋白质编码序列(CDS);采用实时荧光定量PCR(qRT-PCR)技术,检测小菜蛾不同发育阶段个体以及成虫生殖腺中fl(2)d的相对表达量;运用CRISPR/Cas9结合卵的显微注射技术,对小菜蛾fl(2)d进行编辑;将fl(2)d被编辑过的成虫与野生型成虫杂交,并对其产生的后代进行近交,筛选fl(2)d突变品系;观测并比较突变体与野生型个体遗传特性、生物学参数和表型的差异,明确fl(2)d的功能。【结果】克隆得到长度为912 bp的fl(2)d CDS,fl(2)d在雌蛹、雌成虫和卵中的表达量较高,雄成虫和雄蛹的表达量较低,幼虫期的表达量最低,成虫卵巢中表达量显著高于精巢。通过向小菜蛾的卵注射靶向fl(2)d的向导RNA(sgRNA)和Cas9蛋白的混合物,对所产生的阳性后代进行10代的单对近交筛选,获得3种杂合的移码突变品系,分别缺失了4个(Δfl(2)d213-4)、5个(Δfl(2)d213-5)和7个(Δfl(2)d214-7)碱基。在上述品系的筛选过程中,发现了6只缺失4个碱基的纯合突变个体,2只缺失5个碱基的纯合突变个体;缺失4个碱基的纯合个体成功配成了两对,近交未产卵;剩余的2只缺失4个碱基的雄性纯合个体和2只缺失5个碱基的雄性纯合个体分别与同世代的雌性杂合突变个体近交后仍未产卵。说明fl(2)d纯合突变的个体存活率极低,且可能无法产生后代。通过分析后代基因型的分离比,发现杂合突变个体近交以及杂合突变个体与野生型个体杂交产生的后代中,杂合突变个体与野生型个体的比例分别略小于2和1,说明fl(2)d杂合突变会影响小菜蛾正常的生长发育,并导致部分个体死亡。杂合突变体后代中含有突变的雌雄个体比例接近1﹕1(P<0.05),推测小菜蛾fl(2)d可能与性别决定无关。只要是有突变品系小菜蛾所参与的交配,雌成虫产卵量和卵的孵化率均显著低于野生型(P<0.01),所产的卵多数发育异常,表现为失水皱缩、不能正常孵化。通过对成虫的生殖腺进行解剖,发现在野生型雌成虫与突变体雄成虫交配后,卵巢内卵的附着量较未交配的个体明显减少;未交配的突变体雌成虫卵巢内卵的附着量亦少于野生型,而突变体雄成虫的精巢未见明显异常。部分能够孵化的杂合突变个体在整个发育过程会发生不同程度的畸变,导致不能正常完成整个世代;另外一些杂合突变个体未见异常,可以将突变类型遗传给后代。根据上述发现,提出了基于fl(2)d的小菜蛾遗传防控模型。【结论】fl(2)d参与小菜蛾的生殖过程和胚胎发育,突变后显著影响后代种群数量,是开展小菜蛾遗传控制的理想靶标。

关键词: 小菜蛾, fl(2)d, 杂合突变体, 生殖力, 育性

Abstract:

【Objective】 RNA methylation is the main form of epigenetic modification at post-transcriptional level, which is involved in many important cellular processes. The diamondback moth, Plutella xylostella, is an important oligophagous insect pest, causing serious loss on the production of cruciferous vegetables. However, the function of RNA methylation-related genes in P. xylostella is still unclear. The present study aims to identify and clone the homologous fl(2)d, one of the members of the RNA methylation protein complex (writers), to determine the expression pattern offl(2)d, and to knockout fl(2)d using CRISPR/Cas9 for the investigation of its biological functions in P. xylostella.【Method】The sequence of homologous fl(2)d was identified in the genome database ofP. xylostella, which was used for PCR amplification of the coding sequence (CDS). Quantitative real-time PCR (qRT-PCR) was used to study the relative expression levels of fl(2)d in different developmental stages and adult gonads of P. xylostella. The fl(2)d was edited using CRISPR/Cas9 combined with egg injection. Each of the adults that developed from the injected eggs was used to pair with a wild-type adult for reproduction. Offspring of the same population was forced to inbreed by single-pair mating to establish the mutant strains. The differences of genetic characters, biological parameters and phenotypes between mutants and wild-type individuals were recorded and compared to decipher the function offl(2)d.【Result】The CDS of fl(2)d with length of 912 bp was isolated, the expression of which was high in female pupa, adult and egg, moderate in male adult and pupa, the lowest in larva, and significantly higher in ovary than in testis of adult. The sgRNAs targeting fl(2)d and the Cas9 protein were mixed to inject eggs, and the offsprings carrying mutant alleles were screened for homozygous strains based on single-pair inbreeding for 10 generations. Three types of heterozygous mutant strains both predicted to cause frameshift of the CDS were obtained, with the deletion of 4 (Δfl(2)d213-4), 5 (Δfl(2)d213-5) and 7 (Δfl(2)d213-7) bases. During the screening process, six and two homozygous mutants from Δ fl(2)d213-4 and Δ fl(2)d213-5 strains were identified, respectively. The homozygous mutants of Δ fl(2)d213-4 successfully mated in two pairs, but no eggs were produced. Meanwhile, each two male adults of homozygous mutants of either Δ fl(2)d213-4 or Δ fl(2)d213-5 were mated with the same type of female heterozygous mutant, and also no eggs were produced. The results indicated that individuals with homozygousfl(2)d mutation may have extremely low survival rate and not be able to produce offspring. Through analyzing separation ratio of the genotypes of offspring from the inbreeding of heterozygous mutants and the hybridization between heterozygous mutants and wild-type, it was found that the ratio of heterozygous mutant individuals to wild-type was slightly less than 2 and 1, respectively, indicating that heterozygous mutation of fl(2)d would affect the normal growth and development of P. xylostella, and in some cases would lead to death. The offsprings of mutant individuals, which carry a mutant allele, showed a sex ratio close to 1﹕1 (P<0.05). It was speculated that thefl(2)d might not be involved in sex determination in P. xylostella. For the mating consists of mutant adults, the fecundity and hatchability were significantly lower (P<0.01) than the mating between wild-type adults. Most of the eggs produced from the mutant parents look abnormal, and could not hatch normally due to water loss and shrinkage. Based on the dissection of adult gonads, it was found that the number of attached eggs on the ovary of the mutant female adult and the wild-type female adult that has mated with mutant male adult was less than that of the wild-type virgin female adult, while no obvious abnormality was found for the testis of mutant male adult. Some of the hatched heterozygous mutants showed different degrees of distortion during the whole developmental process, resulting in the failure to complete life cycle. A small part of the heterozygous mutant individuals could develop normally, and thus transmit the mutant allele to their offspring. According to our findings, a model of genetic control ofP. xylostella based on fl(2)d was proposed.【Conclusion】The fl(2)d is involved in the reproductive process and embryonic development ofP. xylostella, mutation of which significantly affects the population size of the offspring, making it an ideal target for the genetic control of P. xylostella.

Key words: Plutella xylostella, fl(2)d, heterozygous mutant, fecundity, fertility