Cloning and expression profile of Bmlin-41 and its regulation by the silkworm microRNA let-7.

Lanting ZHOU; Ting ZHOU; Junling GAO; Wei WANG; Xiaoyan WU; Yaxi HUANG; Qingyou XIA; Shiping LIU

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Cloning and expression profile of Bmlin-41 and its regulation by the silkworm microRNA let-7.

Author: Lanting ZHOU ¹ ; Ting ZHOU ¹ ; Junling GAO ¹ ; Wei WANG ¹ ; Xiaoyan WU ¹ ; Yaxi HUANG ¹ ; Qingyou XIA ¹ ; Shiping LIU ¹
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1. State Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400716, China.
Publication Type:Journal Article
Keywords: Bmlin-41; bmo-let-7 miRNA; expression profile; heterochronic gene; silkworm (Bombyx mori); target gene
MeSH: 3' Untranslated Regions; Animals; Bombyx; Cloning, Molecular; DNA, Complementary; Down-Regulation; Drosophila melanogaster; Gene Expression Regulation; Insect Proteins; genetics; metabolism; Metamorphosis, Biological; MicroRNAs; metabolism; Transcription Factors; genetics; metabolism
From: Chinese Journal of Biotechnology 2016;32(5):635-647
CountryChina
Language:Chinese
Abstract: The heterochronic genes regulate cell proliferation and switch development stage transitions. Heterochronic genes might also play important roles in regulating the development of silkworm, but very few of their expression profiles, functions and their relationship with microRNAs are available so far. Firstly, in this work, the primers for cloning Bmlin-41 were designed based on the homologous sequence of known Drosophila melanogaster lin-41, which was used as the query to blast against SilkDB. The obtained full CDS (2 166 bp) of Bmlin-41 encodes 721 amino acids and contains B-box and NHL domains. Then, the spatiotemporal expression patterns of Bmlin-41 were characterized by RT-PCR, quantitative real time PCR as well as our lab's previous silkworm genome microarray data. Bmlin-41 was increasingly expressed from embryonic to adult stage. In diverse tissues of day-3 fifth instar, Bmlin-41 showed the highest accumulation in ovary, secondly in testis and midgut, but very low expression was observed in other tissues. Finally, 3'UTR of Bmlin-41 1 434 bp was cloned by rapid-amplification of cDNA ends (3'RACE) and was predicted to bare two binding sites of bmo-let-7 by using online RNAhybrid. To verify the binding effect, 3'UTR was cloned into psi-CHECK-2 vector and submitted to dual luciferase assay in the S2 cells in vitro. The dual luciferase assay demonstrated that Bmlin-41 was down-regulated by bmo-let-7 mimics and upregulated by bmo-let-7 antagomir, thus confirming the Bmlin-41 is negatively regulated by bmo-let-7. Our work might help further study on the roles of Bmlin-41 and bmo-let-7 and their regulation relationship involved in controlling metamorphosis of silkworm.