首页> 美国卫生研究院文献>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
【2h】

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在体外下调家蚕纤维蛋白轻链基因的表达

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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 larval posterior silk gland (PSG). Firstly, we examined the expression of bmo-miR-0001 and bmo-miR-0015 in 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. To test this hypothesis, we constructed pri-bmo-miR-0001 expressing the plasmid pcDNA3.0 [ie1-egfp-pri-bmo-miR-0001-SV40] 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 [ie1-egfp-pri-bmo-miR-0015-SV40] 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 in vitro.
机译:基于生物信息学分析,我们从家蚕幼虫后丝腺(PSG)的高通量测序中选择了两个新型microRNA(miRNA),即bmo-miR-0001和bmo-miR-0015。首先,我们检查了bmo-miR-0001和bmo-miR-0015在家蚕第五龄第3天幼虫的12种不同组织中的表达。结果显示PSG中bmo-miR-0001和bmo-miR-0015的表达水平明显高于其他组织,这表明bmo-miR-0001和bmo-miR-存在时空条件0015调节BmFib-L的表达。为了验证该假设,我们构建了表达质粒pcDNA3.0 [pri-bmo-miR-0001] [ie1-egfp-pri-bmo-miR-0001-SV40]和pri-bmo-miR-0015表达质粒pcDNA3.0 [ ie1-egfp-pri-bmo-miR-0015-SV40]。最后,收获BmN细胞并检测荧光素酶活性。结果显示,在通过pcDNA3.0 [ie1-egfp-pri-bmo-miR-0001-SV40]或pcDNA3.0 [ie1-egfp-pri-pDNA3.0]共转染的BmN细胞中,萤光素酶活性显着降低(P <0.05)。 bmo-miR-0015-SV40]与pGL3.0 [A3-luc-Fib-L-3'UTR-SV40],表明bmo-miR-0001和bmo-miR-0015均可下调BmFib的表达-L体外。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号