| Literature DB >> 25982022 |
Liang Jiang1, Chunlin Huang1, Qiang Sun1, Huizhen Guo1, Tingcai Cheng1, Zhengwen Peng1, Yinghui Dang1, Weiqiang Liu1, Guowen Xu1, Qingyou Xia2.
Abstract
Introns are important for regulating gene expression. BmAPN4, which has a 5'-UTR upstream intron (5 UI), is specifically expressed in the entire silkworm midgut. In our previous study, the promoter region upstream of the 5 UI of BmAPN4 was cloned and identified as the P3 promoter (P3P) with activity only in the anterior midgut. In this study, the sequence consisting of the P3P and the 5 UI was cloned and named as P3P+5 UI. A transgenic vector was constructed in which EGFP was controlled by P3P+5 UI. Transgenic P3+5 UI silkworms were generated by embryo microinjection. RT-PCR showed P3P+5 UI activity throughout the larval stage. Intense green fluorescence was seen only in the entire midgut of P3+5 UI silkworms and expression was confirmed by RT-PCR. qPCR revealed that expression of EGFP in the anterior midgut of P3+5 UI silkworms was 64% higher than in P3 silkworms, indicating the 5 UI sustained intron-mediated enhancement of gene expression. These results suggested that the BmAPN4 5 UI affected the level and site of expression. The 5 UI was cloned and added behind P2P, another specific promoter with activity only in the anterior midgut of silkworm, to construct the P2P+5 UI and transgenic P2+5 UI silkworms. Expression patterns were the same for P2P+5 UI and P2P, suggesting that the 5UI of BmAPN4 did not affect P2P. This study found that the BmAPN4 5 UI affected the amount and location of gene expression. Its influence appeared to be dependent on a specific promoter.Entities:
Keywords: 5′-UTR intron; IME; Midgut; Promoter; Spatial; Transgenic silkworm
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Year: 2015 PMID: 25982022 DOI: 10.1016/j.ibmb.2015.05.005
Source DB: PubMed Journal: Insect Biochem Mol Biol ISSN: 0965-1748 Impact factor: 4.714