Scientia Agricultura Sinica ›› 2014, Vol. 47 ›› Issue (7): 1313-1320.doi: 10.3864/j.issn.0578-1752.2014.07.008

• Insect chitin metabolism and plant protection • Previous Articles     Next Articles

Molecular Characterization and Function of Chitinase 10 Gene (OcCht10) from Oxya chinensis

 LI  Da-Qi-1, WANG  Yan-1, ZHANG  Jian-Qin-1, LI  Tao-1, SUN  Yi-2, ZHANG  Jian-Zhen-1   

  1. 1、Research Institute of Applied Biology, Shanxi University, Taiyuan 030006;
    2、Biotechnology Research Center, Shanxi Academy of Agricultural Sciences, Taiyuan 030031
  • Received:2013-10-24 Online:2014-04-01 Published:2013-11-05

Abstract: 【Objective】 The objectives of this study are to obtain cDNA sequence of chitinase 10 gene (OcCht10) from Oxya chinensis, analyze its functional domain and phylogenetic relationship with chitinases from other known insect species, investigate its expression patterns and biological function during molting process, and to provide a new candidate gene for pest control.【Method】 cDNA fragments of OcCht10 were searched from O. chinensis’ transcriptome database. After blast analysis, the cDNA sequence of OcCht10 was assembled and translated, the functional domains of OcCht10 were predicted by bioinformatics methods. Phylogenetic analysis was performed with other insect chitinase 10 amino acid sequences. The first-stranded cDNAs were synthesized by using RNA isolated from integument of each day of 5th instar nymphs and various tissues of the 6th day in 5th instar nymphs. Reverse transcription quantitative PCR (qPCR) was carried out to analyze the gene expression patterns. Biological function of OcCht10 was studied by RNA interference method. The dsRNA primers were designed for dsOcCht10 synthesis in vitro. The dsRNAs were injected into the 2nd day of 5th instar nymphs for RNA interference, integument was dissected for silencing efficiency detection at 24 h after injection by using qPCR method. The phenotype was carefully observed and mortality was calculated till control insects molted to adults.【Result】 The obtained cDNA (9 318 bp) of OcCht10 contained an open reading frame of 8 613 bp, encoding 2 870 amino acid residues and a non-coding region of 705 bp at 3′ end. There were about 500 bp lost in 5′ end. The deduced amino acid sequence included five chitinase catalytic domains and six chitin binding domains. Phylogenetic analysis showed that OcCht10 belonged to chitinase group Ⅱ, the genes from this group were crucial for insect molting based on references. Tissue specific expression analysis of OcCht10 showed that it was predominately expressed in the integument, foregut and hindgut, which developed from ectoderm. The results suggested that OcCht10 may be involved in chitin metabolism of insect integument. Developmental expression patterns showed that OcCht10 was highly expressed before and after molting stages, lower in middle stages of 5th instar nymphs, which implied that OcCht10 could digest chitin of integument during molting process. RNA interference results indicated that the corresponding transcript level was silenced by 70% after OcCht10 dsRNA injection. Compared with the dsGFP injected control group, the nymphs injected with OcCht10 dsRNA displayed slow development and failed to detach old cuticle during molting, the mortality reached 100%.【Conclusion】 The partial cDNA sequence of OcCht10 was obtained from O. chinensis, the mRNA expression of OcCht10 was higher in the integument before molting; OcCht10 is involved in O. chinensis molting process, and dsOcCht10 injection can effectively silence mRNA expression of this gene and result in the block of ecdysis and even death of O. chinensis.

Key words: Oxya chinensis, chitinase gene, reverse transcription quantitative PCR, RNA interference

[1]Merzendorfer H. Insect chitin synthases: a review. Journal of Comparative Physiology B, 2006, 176: 1-15.

[2]Vega H, Specht C A, Liu Y, Robbins P W. Chitinases are a multi-gene family in Aedes, Anopheles and Drosophila. Insect Molecular Biology, 1998, 7(3): 233-239.

[3]Zhu Q, Deng Y, Vanka P, Brown S J, Muthukrishnan S, Kramer K J. Computational identification of novel chitinase-like proteins in the Drosophila melanogaster genome. Bioinformatics, 2004, 20(2): 161-169.

[4]Zhu Q, Arakane Y, Banerjee D, Beeman R W, Kramer K J, Muthukrishnan S. Domain organization and phylogenetic analysis of the chitinase-like family of proteins in three species of insects. Insect Biochemistry and Molecular Biology, 2008, 38: 452-466.

[5]Zhang J Z, Zhang X, Arakane Y, Muthukrishnan S, Kramer K J, Ma E B, Zhu K Y. Comparative genomic analysis of chitinase and chitinase-like genes in the African Malaria mosquito (Anopheles gambiae). PLoS ONE, 2011, 6(5): e19899.

[6]Nakabachi A, Shigenobu S, Miyagishima S. Chitinase-like proteins encoded in the genome of the pea aphid, Acyrthosiphon pisum. Insect Molecular Biology, 2010, 19(Suppl.2): 175-185.

[7]Pan Y, Lü P, Wang Y, Yin L J, Ma H X, Ma G H, Chen K P, He Y Q. In silico identification of novel chitinase-like proteins in the silkworm, Bombyx mori, genome. Journal of Insect Science, 2012, 12: Article 150.

[8]李大琪, 杜建中, 张建琴, 郝耀山, 刘晓健, 王亦学, 马恩波, 张建珍, 孙毅. 东亚飞蝗几丁质酶家族基因的表达特性与功能研究. 中国农业科学, 2011, 44(3): 485-492.

Li D Q, Du J Z, Zhang J Q, Hao Y S, Liu X J, Wang Y X, Ma E B, Zhang J Z, Sun Y. Study on expression characteristics and functions of chitinase family genes from Locusta migratoria manilensis (Meyen). Scientia Agricultura Sinica, 2011, 44(3): 485-492. (in Chinese)

[9]Zhu Q, Arakane Y, Beeman R W, Kramer K J, Muthukrishnan S. Functional specialization among insect chitinase family genes revealed by RNA interference. Proceedings of the National Academy of Sciences of the United States of America, 2008, 105(18): 6650-6655.

[10]Khajuria C, Buschman L L, Chen M S , Muthukrishnan S, Zhu K Y. A gut-specific chitinase gene essential for regulation of chitin content of peritrophic matrix and growth of Ostrinia nubilalis larvae. Insect Biochemistry and Molecular Biology, 2010, 40: 621-629.

[11]Shi L, Paskewitz S M. Identification and molecular characterization of two immune-responsive chitinase-like proteins from Anopheles gambiae. Insect Molecular Biology, 2004, 13(4): 387-398.

[12]Kawamura K, Shibata T, Saget O, Peel D, Bryant P J. A new family of growth factors produced by the fat body and active on Drosophila imaginal disc cells. Development, 1999, 126: 211-219.

[13]Schultz J, Milpetz F, Bork P, Ponting C P. SMART, a simple modular architecture research tool: Identification of signaling domains. Proceedings of the National Academy of Sciences of the United States of America, 1998, 95: 5857-5864.

[14]Pfaffl M W. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Research, 2001, 29(9): 2002-2007.

[15]Arziman Z, Horn T, Boutros M. E-RNAi: a web application to design optimized RNAi constructs. Nucleic Acids Research, 2005, 33: 582-588.

[16]Arakane Y, Muthukrishnan S. Insect chitinase and chitinase-like proteins. Cellular and Molecular Life Sciences, 2010, 67: 201-216.

[17]Yan J, Cheng Q, Narashimhan S, Li C B, Aksoy S. Cloning and functional expression of a fat body-specific chitinase cDNA from the tsetse fly, Glossina morsitans morsitans. Insect Biochemistry and Molecular Biology, 2002, 32: 979-989.

[18]Krishnan A, Nair P N, Jones D. Isolation, cloning, and characterization of new chitinase stored in active form in chitin-lined venom reservoir. The Journal of Biological Chemistry, 1994, 269(33): 20971-20976.

[19]Royer V, Fraichard S, Bouhin H. A novel putative insect chitinase with multiple catalytic domains: hormonal regulation during metamorphosis. Biochemical Journal, 2002, 366: 921-928.

[20]Tomoyasu Y, Miller S C, Tomita S, Schoppmeier M, Grossmann D, Buche G. Exploring systemic RNA interference in insects: a genome-wide survey for RNAi genes in Tribolium. Genome Biology, 2008, 9: R10.

[21]Dong Y, Friedrich M. Nymphal RNAi: Systemic RNAi mediated gene knockdown in juvenile grasshopper. BMC Biotechnology, 2005, 5: 25-32.

[22]Zhang J Z, Zhang J Q, Yang M L, Jia Q D, Guo Y P, Ma E B, Zhu K Y. Genomics-based approaches to screening carboxylesterase-like genes potentially involved in malathion resistance in oriental migratory locust (Locusta migratoria manilensis). Pest Management Science, 2011, 67: 183-190.

[23]Price D R G, Gatehouse J A. RNAi-mediated crop protection against insects. Cell, 2008, 26(7): 393-400.

[24]Mao Y B, Cai W J, Wang J W, Hong G J, Tao X Y, Wang L J, Huang Y P, Chen X Y. Silencing a cotton bollworm P450 monooxygenase gene by plant-mediated RNAi impairs larval tolerance of gossypol. Nature Biotechnology, 2007, 25(11): 1307-1313.

[25]Zhu J Q, Liu S M, Ma Y, Zhang J Q, Qi H S, Wei Z J, Yao Q, Zhang W Q, Li S. Improvement of pest resistance in transgenic tobacco plants expressing dsRNA of an insect-associated gene EcR. PLoS ONE, 2012, 7(6): e38572.

[26]Baum J A, Bogaert T, Clinton W, Heck G R, Feldmann P, Ilagan O, Johnson S, Plaetinck G, Munyikwa T, Pleau M, Vaughn T, Roberts J. Control of coleopteran insect pests through RNA interference. Nature Biotechnology, 2007, 25(11): 1322-1326.

[27]Mao Y B, Tao X Y, Xue X Y, Wang L J, Chen X Y. Cotton plants expressing CYP6AE14 double-stranded RNA show enhanced resistance to bollworms. Transgenic Research, 2011, 20: 665-673.

[28]He B C, Chu Y, Yin M Z, Müllen K, An C J, Shen J. Fluorescent nanoparticle delivered dsRNA toward genetic control of insect pests. Advanced Materials, 2013, 25: 4580-4584.

[29]Khan A M, Ashfaq M, Kiss Z, Khan A A, Mansoor S, Falk B W. Use of recombinant Tobacco mosaic virus to achieve RNA interference in plants against the citrus mealybug Planococcus citri (Hemiptera: Pseudococcidae). PLoS ONE, 2013, 8(9): e73657.
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