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Molecular Cloning and Expression of a Cysteine Gene in Empoasca onukii

  • YU Yongchen ,
  • XIAO Bin ,
  • SUN Xiaoling
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  • 1. Northwest A&F University, Yangling 712100, China;
    2. Tea Research Institute of Chinese Academy of Agricultural Sciences, Hangzhou 310008, China;
    3. Key Laboratory of Tea Biology and Resource Utilization of Ministry of Agriculture, Hangzhou 310008, China

Received date: 2018-01-18

  Revised date: 2018-03-26

  Online published: 2019-08-28

Abstract

Cysteine proteinases are important proteolytic enzymes for herbivorous insects. In this paper, the transcript sequence of Eocyp was obtained from the transcriptome database of Empoasca onukii. The full-length cDNA sequence of Eocyp was then cloned by RACE. The theoretical amino acid sequence of Eocyp was analyzed by bioinformatics. The expression levels of Eocyp in different developmental stages, different parts of female and male adults of E. onukii and nymphs under different temperatures and photoperiods were detected by qRT-PCR. The full-length cDNA sequence of Eocyp contained an open reading frame of 1β656βbp, which encoded 551 amino acids and had a signal peptide consisting of 24 amino acid residues. Its molecular formula was predicted to be C2782H4163N737O835S25. Its relative molecular weight and the theoretical isoelectric point were estimated to be 62.09βkD and 6.02, and the instability coefficient of Eocyp was 36.10. Eocyp had the typical feature of cysteine protease, a catalytic triad Cys357-His499-Asn519, and the conserved domains such as ERFNIN, GNFD amino acid residues and the GCDGG clusters. The amino acid sequence of Eocyp had a high similarity with the CYP gene of Halyomorpha halys. Expression analysis showed that Eocyp was expressed in all developmental stages of E. onukii with its peak in the fifth instar nymphs. Higher expression of Eocyp was observed in the abdomen of adult E. onukii, irrespective of female and male. However, the expression level of Eocyp did not respond to the variation of temperatures and photoperiods. These results provided a theoretical basis for further study of Eocyp.

Cite this article

YU Yongchen , XIAO Bin , SUN Xiaoling . Molecular Cloning and Expression of a Cysteine Gene in Empoasca onukii[J]. Journal of Tea Science, 2018 , 38(3) : 263 -270 . DOI: 10.13305/j.cnki.jts.2018.03.006

References

[1] Berti P J, Storer A C.Alignment/phylogeny of the papain superfamily of cysteine proteases[J]. Journal of Molecular Biology, 1995, 246(2): 273-283.
[2] Chernaya V I.Early Postnatal Development-related dynamics of the activity of cathepsin l in rat brain structures[J]. Neurophysiology, 2001, 33(1): 15-18.
[3] Barros N M, Puzer L, Tersariol I L, et al.Plasma prekallikrein/kallikrein processing by lysosomal cysteine proteases[J]. Biological Chemistry, 2004, 385(11): 1087-1091.
[4] Cristofoletti P T, Ribeiro A F, Deraison C, et al.Midgut adaptation and digestive enzyme distribution in a phloem feeding insect, the pea aphid Acyrthosiphon pisum[J]. Journal of Insect Physiology, 2003, 49(1): 11-24.
[5] Rabossi A, Stoka V, Puizdar V, et al.Novel aspartyl proteinase associated to fat body histolysis during Ceratitis capitata early metamorphosis[J]. Archives of Insect Biochemistry & Physiology, 2004, 57(2): 51-67.
[6] Zhao X, An X, Wang J, et al.Expression of the Helicoverpa cathepsin b-like proteinase during embryonic development[J]. Arch Insect Biochem Physiol, 2005, 58(1): 39-46.
[7] Liu J, Shi G P, Zhang W Q, et al.Cathepsin L function in insect moulting: molecular cloning and functional analysis in cotton bollworm, Helicoverpa armigera[J]. Insect Molecular Biology, 2006, 15(6): 823-834.
[8] Beton D, Guzzo C R, Ribeiro A F, et al.The 3D structure and function of digestive cathepsin L-like proteinases of Tenebrio molitor larval midgut[J]. Insect Biochemistry & Molecular Biology, 2012, 42(9): 655-664.
[9] L F Wang, L Q Chai, He H J, et al. A cathepsin L-like proteinase is involved in moulting and metamorphosis in Helicoverpa armigera[J]. Insect Molecular Biology, 2010, 19(1): 99-111.
[10] Kwangsik L, Boyeon K, Youngmoo C, et al.Expression profile of cathepsin B in the fat body of Bombyx mori during metamorphosis[J]. Comparative Biochemistry & Physiology Part B Biochemistry & Molecular Biology, 2009, 154(2): 188-194.
[11] Yu J, Wu F Y, Zou F M, et al.Identification of ecdysone response elements (EcREs) in the Bombyx mori cathepsin D promoter[J]. Biochemical & Biophysical Research Communications, 2012, 425(1): 113-118.
[12] Cai X Y, Yu J, Yu H Y, et al.Core promoter regulates the expression of cathepsin B gene in the fat body of Bombyx mori[J]. Gene, 2014, 542(2): 232-239.
[13] 苏晶晶, 陈思源, 张奎, 等. 家蚕组织蛋白酶O (BmCatO) 基因鉴定及表达分析[J]. 中国农业科学, 2015, 48(22): 4564-4573.
[14] Wu F, Kang L, Wang P, et al.The expression analysis of cysteine proteinase-like protein in wild-type and nm2 mutant silkworm (Lepidoptera: Bombyx mori)[J]. Gene, 2016, 586(1): 170-175.
[15] Peter M, Turnšek N, Gašparič MB, et al.A complex of genes involved in adaptation of Leptinotarsa decemlineata larvae to induced potato defense[J]. Arch Insect Biochem Physiol, 2012, 79(3): 153-181.
[16] 赵冬香, 陈宗懋, 程家安. 茶小绿叶蝉优势种的归属[J]. 茶叶科学, 2000, 20(2): 101-104.
[17] 王念武, 徐金汉, 陈峥, 等. 不同茶园假眼小绿叶蝉抗药性比较[J]. 福建农业大学学报, 2004(2): 169-173.
[18] 庄家祥, 傅建炜, 苏庆泉, 等. 福建省茶小绿叶蝉抗药性的地区差异[J]. 茶叶科学, 2009, 29(2): 154-158.
[19] Bolter C, Jongsma M A.The adaptation of insect to plant protease inhibitors[J]. Journal of Insect Physiology. 1997, 43(10): 885-895.
[20] 杨文佳, 许抗抗, 王进军, 等. 橘小实蝇半胱氨酸蛋白酶基因克隆及表达模式[J]. 中山大学学报(自然科学版), 2017, 56(1): 131-137.
[21] 宋旺. 花绒寄甲Caspase-1基因的表达研究[D]. 杨凌: 西北农林科技大学, 2014.
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