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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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 |
work_keys_str_mv |
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1716813976579342336 |