Characterization of three transcripts encoding small heat shock proteins expressed in the codling moth, Cydia pomonella （Lepidoptera： Tortricidae）  

作　　者：Stephen F. Garczynski Thomas R. Unruh Christelle Guedot Lisa G. Neven 

机构地区：[1]USDA-ARS, Yakima Agricultural Research Laboratory, Wapato, Washington, USA

出　　处：《Insect Science》2011年第5期473-483,共11页昆虫科学（英文版）

摘　　要：Codling moth is a major pest of apples and pears worldwide. Increasing knowledge of how this insect responds to environmental stress will improve field and postharvest control measures used against it. The small heat shock proteins （sHsps） play a maj or role in cellular responses to environmental stressors. A degenerate oligonucleotide primer, designed against the conserved α-crystallin domain, was used in 3＇ rapid amplification of complementary DNA （cDNA） ends reactions to amplify transcripts encoding sHsps expressed in the codling moth cell line, Cp169, subjected to heat shock. Three full-length cDNAs were cloned from Cp169 cells that contained open reading frames encoding sHsps. The cDNA for CpHsp 19.8 was 795 bp encoding 177 amino acids. The cDNA for CpHsp 19.9 was 749 bp encoding 175 amino acids. The cDNA for CpHsp22.2 was 737 bp encoding 192 amino acids. Analysis of the protein sequences of the three CpHsps indicated the presence of 83 amino acids with homology to the α-crystallin domain. For each of the CpHsps, the α-crystallin domain was surrounded by divergent N- and C-terminal regions, consistent with the conserved structural features of sHsps. Real-time polymerase chain reaction, used to determine the expression patterns of each of the sHsps in different developmental stages of codling moth revealed the presence of transcripts in all stages tested. Consistent with characteristics of other sHsps, expression of CpHsp transcripts were greatly enhanced when insects were subjected to heat shock. The results of this research can be used as a guide to study the roles of sHsps in codling moth control using various post-harvest treatments.Codling moth is a major pest of apples and pears worldwide. Increasing knowledge of how this insect responds to environmental stress will improve field and postharvest control measures used against it. The small heat shock proteins （sHsps） play a maj or role in cellular responses to environmental stressors. A degenerate oligonucleotide primer, designed against the conserved α-crystallin domain, was used in 3＇ rapid amplification of complementary DNA （cDNA） ends reactions to amplify transcripts encoding sHsps expressed in the codling moth cell line, Cp169, subjected to heat shock. Three full-length cDNAs were cloned from Cp169 cells that contained open reading frames encoding sHsps. The cDNA for CpHsp 19.8 was 795 bp encoding 177 amino acids. The cDNA for CpHsp 19.9 was 749 bp encoding 175 amino acids. The cDNA for CpHsp22.2 was 737 bp encoding 192 amino acids. Analysis of the protein sequences of the three CpHsps indicated the presence of 83 amino acids with homology to the α-crystallin domain. For each of the CpHsps, the α-crystallin domain was surrounded by divergent N- and C-terminal regions, consistent with the conserved structural features of sHsps. Real-time polymerase chain reaction, used to determine the expression patterns of each of the sHsps in different developmental stages of codling moth revealed the presence of transcripts in all stages tested. Consistent with characteristics of other sHsps, expression of CpHsp transcripts were greatly enhanced when insects were subjected to heat shock. The results of this research can be used as a guide to study the roles of sHsps in codling moth control using various post-harvest treatments.

关 键 词：α-crystallin domain heat shock response qPCR 

分 类 号：Q51[生物学—生物化学] S436.611.2[农业科学—农业昆虫与害虫防治]