Hong-bo JIANG , Guang-mao SHEN , Wei DOU , Pei-an TANG , Yong-hua LIU , An-wei ZHOU , Jin-jun WANG
{"title":"嗜脂囊蝇β-肌动蛋白基因的鉴定与表达(鞘翅目:脂囊蝇科)","authors":"Hong-bo JIANG , Guang-mao SHEN , Wei DOU , Pei-an TANG , Yong-hua LIU , An-wei ZHOU , Jin-jun WANG","doi":"10.1016/S1671-2927(11)60132-6","DOIUrl":null,"url":null,"abstract":"<div><p>A <em>β-actin</em> gene, <em>Libβ-actinl</em>, from the psocid, <em>Liposcelis bostrychophila</em>, was isolated, sequenced, and expressed in <em>Escherichia coli.</em> The cDNA sequence was 1 281 bp in length and contained an open reading frame of 1 131 bp encoding 376 amino acids with a predicted molecular weight of 41.82 kDa. According to a BlastN search, the coding region shared the highest identity (97%) with <em>Pediculus humanus actin 5C</em>, while the deduced amino acid sequence was completely identical to a mutant of <em>Drosophila melanogaster actin 5C.</em> Comparison of the nucleotide and deduced amino acid sequences confirmed the high similarity between <em>Libβ-actinl</em> and homologs in other insect species. The 3′ untranslated region (3′ UTR) of the <em>Libβ-actinl</em> mRNA had a high A+U content (approximately 75%) and contained three repeats of the AUUUUUA and AUUUA motifs, which may play a role in regulating mRNA decay. The expression of <em>Libβ-actinl</em> was further analyzed in insecticide induced and control psocids. The results indicated that there was no significant difference in expression of <em>Libβ-actinl</em> between the induced and control groups, suggesting that <em>Libβ-actinl</em> may be an appropriate internal control for the gene expression profiling in this insect. Furthermore, <em>Libβ-actinl</em> was also heterologously expressed in <em>Escherichia coli</em>, which provided a basis to investigate the physiological functions of actin genes in the psocid.</p></div>","PeriodicalId":7475,"journal":{"name":"Agricultural Sciences in China","volume":"10 9","pages":"Pages 1391-1401"},"PeriodicalIF":0.0000,"publicationDate":"2011-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1671-2927(11)60132-6","citationCount":"4","resultStr":"{\"title\":\"Identification and Expression of a β-actin Gene from Liposcelis bostrychophila Badonnel (Psocoptera: Liposcelididae)\",\"authors\":\"Hong-bo JIANG , Guang-mao SHEN , Wei DOU , Pei-an TANG , Yong-hua LIU , An-wei ZHOU , Jin-jun WANG\",\"doi\":\"10.1016/S1671-2927(11)60132-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A <em>β-actin</em> gene, <em>Libβ-actinl</em>, from the psocid, <em>Liposcelis bostrychophila</em>, was isolated, sequenced, and expressed in <em>Escherichia coli.</em> The cDNA sequence was 1 281 bp in length and contained an open reading frame of 1 131 bp encoding 376 amino acids with a predicted molecular weight of 41.82 kDa. According to a BlastN search, the coding region shared the highest identity (97%) with <em>Pediculus humanus actin 5C</em>, while the deduced amino acid sequence was completely identical to a mutant of <em>Drosophila melanogaster actin 5C.</em> Comparison of the nucleotide and deduced amino acid sequences confirmed the high similarity between <em>Libβ-actinl</em> and homologs in other insect species. The 3′ untranslated region (3′ UTR) of the <em>Libβ-actinl</em> mRNA had a high A+U content (approximately 75%) and contained three repeats of the AUUUUUA and AUUUA motifs, which may play a role in regulating mRNA decay. The expression of <em>Libβ-actinl</em> was further analyzed in insecticide induced and control psocids. The results indicated that there was no significant difference in expression of <em>Libβ-actinl</em> between the induced and control groups, suggesting that <em>Libβ-actinl</em> may be an appropriate internal control for the gene expression profiling in this insect. Furthermore, <em>Libβ-actinl</em> was also heterologously expressed in <em>Escherichia coli</em>, which provided a basis to investigate the physiological functions of actin genes in the psocid.</p></div>\",\"PeriodicalId\":7475,\"journal\":{\"name\":\"Agricultural Sciences in China\",\"volume\":\"10 9\",\"pages\":\"Pages 1391-1401\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2011-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S1671-2927(11)60132-6\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Agricultural Sciences in China\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1671292711601326\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Agricultural Sciences in China","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1671292711601326","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Identification and Expression of a β-actin Gene from Liposcelis bostrychophila Badonnel (Psocoptera: Liposcelididae)
A β-actin gene, Libβ-actinl, from the psocid, Liposcelis bostrychophila, was isolated, sequenced, and expressed in Escherichia coli. The cDNA sequence was 1 281 bp in length and contained an open reading frame of 1 131 bp encoding 376 amino acids with a predicted molecular weight of 41.82 kDa. According to a BlastN search, the coding region shared the highest identity (97%) with Pediculus humanus actin 5C, while the deduced amino acid sequence was completely identical to a mutant of Drosophila melanogaster actin 5C. Comparison of the nucleotide and deduced amino acid sequences confirmed the high similarity between Libβ-actinl and homologs in other insect species. The 3′ untranslated region (3′ UTR) of the Libβ-actinl mRNA had a high A+U content (approximately 75%) and contained three repeats of the AUUUUUA and AUUUA motifs, which may play a role in regulating mRNA decay. The expression of Libβ-actinl was further analyzed in insecticide induced and control psocids. The results indicated that there was no significant difference in expression of Libβ-actinl between the induced and control groups, suggesting that Libβ-actinl may be an appropriate internal control for the gene expression profiling in this insect. Furthermore, Libβ-actinl was also heterologously expressed in Escherichia coli, which provided a basis to investigate the physiological functions of actin genes in the psocid.