首页> 外文期刊>Journal of Zhejiang University. Science, B >bmo-miR-0001 and bmo-miR-0015 down-regulate expression of Bombyx mori fibroin light chain gene in vitro
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bmo-miR-0001 and bmo-miR-0015 down-regulate expression of Bombyx mori fibroin light chain gene in vitro

机译:BMO-MIR-0001和BMO-MIR-0015在体外下调Bombyx Mori纤维素轻链基因的调节表达

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Based on bioinformatic analysis, we selected two novel microRNAs (miRNAs), bmo-miR-0001 and bmo-miR-0015, from high-throughput sequencing of the Bombyx mori%29&ck%5B%5D=abstract&ck%5B%5D=keyword'>Bombyx mori larval posterior silk gland (PSG). Firstly, we examined the expression of bmo-miR-0001 and bmo-miR 12 different tissues of the 5th instar Day-3 larvae of the silkworm. The results showed that the expression levels of both bmo-miR-0001 and bmo-miR-0015 were obviously higher in the PSG than in other tissues, implying there is a spatio-temporal condition for bmo-miR-0001 and bmo-miR-0015 to regulate the expression of BmFib-L%29&ck%5B%5D=abstract&ck%5B%5D=keyword'>BmFib-L. To test this hypothesis, we constructed pri-bmo-miR-0001 expressing the plasmid pcDNA3.0 and pri-bmo-miR-0015 expressing the plasmid pcDNA3.0 [ie1-egfp-pri-bmo-miR-0015-SV40]. Finally, the BmN cells were harvested and luciferase activity was detected. The results showed that luciferase activity was reduced significantly (P<0.05) in BmN cells co-transfected by pcDNA3.0 [ie1-egfp-pri-bmo-miR-0001-SV40] or pcDNA3.0 with pGL3.0 [A3-luc-Fib-L-3'UTR-SV40], suggesting that both bmo-miR-0001 and bmo-miR-0015 can down-regulate the expression of BmFib-L%29&ck%5B%5D=abstract&ck%5B%5D=keyword'>BmFib-L in vitro.
机译:基于生物信息分析,我们选择了两种新的MicroRNAS(MIRNA),BMO-MIR-0001和BMO-MIR-0015,来自BOMBYX MORI%29的高通量测序&CK%5B%5d = Abstract&CK%5b%5d =关键字' > Bombyx Mori Larval后丝丝腺(PSG)。首先,我们研究了BMO-MIR-0001和BMO-MIR 12的第5次胰素幼虫的BMO-MIR 12不同组织的表达。结果表明,BMO-miR-0001和BMO-miR-0015的表达水平在PSG中显然比其他组织明显较高,这意味着BMO-MIR-0001和BMO-MIR的时空条件0015调节BMFIB-L%29和CK%5B%5d =摘要&ck%5b%5d =关键词'bmfib-l的表达。为了测试该假设,我们构建了表达质粒pCDNA3.0的PRI-BMO-miR-0001和表达质粒pCDNA3.0的PRI-BMO-MIR-0015 [IE1-EGFP-PRI-BMO-MIR-0015-SV40]。最后,收获BMN细胞并检测荧光素酶活性。结果表明,通过PCDNA3.0 [IE1-EGFP-PRI-BMO-MIR-0001-SV40]或PCDNA3.0与PGL3.0(PCDNA3.0)显着降低了荧光素酶活性(P <0.05)中的BMN细胞Luc-Fib-L-3'UTR-SV40],表明BMO-MIR-0001和BMO-MIR-0015可以降低BMFIB-L%29和CK%5B%5D =摘要和CK%5B%5d =关键词'> BMFIB-L体外。

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