Molecular characterization of the giant freshwater prawn (Macrobrachium rosenbergii) beta-actin gene promoter

Constitutive promoters are important tools for gene function studies and transgenesis. The Beta-actin (actb1) gene promoter has been isolated from many species but remains to be cloned from the giant freshwater prawn (Macrobrachium rosenbergii). In this study, we cloned and characterized the Mractb1...

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Main Authors: Junjun Yan, Qiang Gao, Zongbin Cui, Guoliang Yang, Yong Long
Format: Article
Language:English
Published: PeerJ Inc. 2018-10-01
Series:PeerJ
Subjects:
Online Access:https://peerj.com/articles/5701.pdf
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spelling doaj-6b195be68aae41fa9d0bddb9b8ecf6072020-11-24T20:45:48ZengPeerJ Inc.PeerJ2167-83592018-10-016e570110.7717/peerj.5701Molecular characterization of the giant freshwater prawn (Macrobrachium rosenbergii) beta-actin gene promoterJunjun Yan0Qiang Gao1Zongbin Cui2Guoliang Yang3Yong Long4State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, ChinaZhejiang Institute of Freshwater Fisheries, Huzhou, ChinaState Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, ChinaHuzhou University, Huzhou, ChinaState Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, ChinaConstitutive promoters are important tools for gene function studies and transgenesis. The Beta-actin (actb1) gene promoter has been isolated from many species but remains to be cloned from the giant freshwater prawn (Macrobrachium rosenbergii). In this study, we cloned and characterized the Mractb1 gene promoter. Two alternative promoters were identified for the Mractb1 gene, which direct the generation of two transcripts with different 5′ untranslated regions. Three CpG islands were predicted in the upstream sequence, which are intimately related to transcription initiation and promoter activity. In addition to the CCAAT-box and the CArG-box, molecular dissection of the flanking sequence revealed the existence of one negative and two positive elements in the upstream region and the first intron. Finally, the Mractb1 promoter demonstrated comparative activity to the carp (Cyprinus carpio) actb1 promoter. Our investigations provide a valuable genetic tool for gene function studies and shed light on the regulation of the Mractb1 gene.https://peerj.com/articles/5701.pdfGiant freshwater prawnBeta-actin genePromoterTranscriptional activity
collection DOAJ
language English
format Article
sources DOAJ
author Junjun Yan
Qiang Gao
Zongbin Cui
Guoliang Yang
Yong Long
spellingShingle Junjun Yan
Qiang Gao
Zongbin Cui
Guoliang Yang
Yong Long
Molecular characterization of the giant freshwater prawn (Macrobrachium rosenbergii) beta-actin gene promoter
PeerJ
Giant freshwater prawn
Beta-actin gene
Promoter
Transcriptional activity
author_facet Junjun Yan
Qiang Gao
Zongbin Cui
Guoliang Yang
Yong Long
author_sort Junjun Yan
title Molecular characterization of the giant freshwater prawn (Macrobrachium rosenbergii) beta-actin gene promoter
title_short Molecular characterization of the giant freshwater prawn (Macrobrachium rosenbergii) beta-actin gene promoter
title_full Molecular characterization of the giant freshwater prawn (Macrobrachium rosenbergii) beta-actin gene promoter
title_fullStr Molecular characterization of the giant freshwater prawn (Macrobrachium rosenbergii) beta-actin gene promoter
title_full_unstemmed Molecular characterization of the giant freshwater prawn (Macrobrachium rosenbergii) beta-actin gene promoter
title_sort molecular characterization of the giant freshwater prawn (macrobrachium rosenbergii) beta-actin gene promoter
publisher PeerJ Inc.
series PeerJ
issn 2167-8359
publishDate 2018-10-01
description Constitutive promoters are important tools for gene function studies and transgenesis. The Beta-actin (actb1) gene promoter has been isolated from many species but remains to be cloned from the giant freshwater prawn (Macrobrachium rosenbergii). In this study, we cloned and characterized the Mractb1 gene promoter. Two alternative promoters were identified for the Mractb1 gene, which direct the generation of two transcripts with different 5′ untranslated regions. Three CpG islands were predicted in the upstream sequence, which are intimately related to transcription initiation and promoter activity. In addition to the CCAAT-box and the CArG-box, molecular dissection of the flanking sequence revealed the existence of one negative and two positive elements in the upstream region and the first intron. Finally, the Mractb1 promoter demonstrated comparative activity to the carp (Cyprinus carpio) actb1 promoter. Our investigations provide a valuable genetic tool for gene function studies and shed light on the regulation of the Mractb1 gene.
topic Giant freshwater prawn
Beta-actin gene
Promoter
Transcriptional activity
url https://peerj.com/articles/5701.pdf
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AT zongbincui molecularcharacterizationofthegiantfreshwaterprawnmacrobrachiumrosenbergiibetaactingenepromoter
AT guoliangyang molecularcharacterizationofthegiantfreshwaterprawnmacrobrachiumrosenbergiibetaactingenepromoter
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