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Regulation of RNase E during the UV stress response in the cyanobacterium Synechocystis sp.PCC 6803
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作者 satoru watanabe Damir Stazic +8 位作者 Jens Georg Shota Ohtake Yutaka Sakamaki Megumi Numakura Munehiko Asayama Taku Chibazakura Annegret Wilde Claudia Steglich Wolfgang R.Hess 《mLife》 CSCD 2023年第1期43-57,共15页
Endoribonucleases govern the maturation and degradation of RNA and are indispensable in the posttranscriptional regulation of gene expression.A key endoribonuclease in Gram-negative bacteria is RNase E.To ensure an ap... Endoribonucleases govern the maturation and degradation of RNA and are indispensable in the posttranscriptional regulation of gene expression.A key endoribonuclease in Gram-negative bacteria is RNase E.To ensure an appropriate supply of RNase E,some bacteria,such as Escherichia coli,feedback-regulate RNase E expression via the rne 5′-untranslated region(5′UTR)in cis.However,the mechanisms involved in the control of RNase E in other bacteria largely remain unknown.Cyanobacteria rely on solar light as an energy source for photosynthesis,despite the inherent ultraviolet(UV)irradiation.In this study,we first investigated globally the changes in gene expression in the cyanobacterium Synechocystis sp.PCC ^(6)803 after a brief exposure to UV.Among the 407 responding genes 2 h after UV exposure was a prominent upregulation of rne mRNA level.Moreover,the enzymatic activity of RNase E rapidly increased as well,although the protein stability decreased.This unique response was underpinned by the increased accumulation of full-length rne mRNA caused by the stabilization of its 5′UTR and suppression of premature transcriptional termination,but not by an increased transcription rate.Mapping of RNA 3′ends and in vitro cleavage assays revealed that RNase E cleaves within a stretch of six consecutive uridine residues within the rne 5′UTR,indicating autoregulation.These observations suggest that RNase E in cyanobacteria contributes to reshaping the transcriptome during the UV stress response and that its required activity level is secured at the RNA level despite the enhanced turnover of the protein. 展开更多
关键词 CYANOBACTERIA protein turnover RIBONUCLEASE stress response
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利用日本多中心数据库对人工神经网络进行再训练以探测心肌缺血 被引量:3
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作者 刘颍桦(译) 唐军(审校) 《中华核医学与分子影像杂志》 CAS 北大核心 2018年第10期710-710,共1页
目的人工神经网络(ANN)已被应用于探测心肌灌注缺损和缺血。该研究的目的是比较最新1.1版本的ANN与最初1.0版本的诊断准确性。方法研究了106例冠状动脉(简称冠脉)造影阳性的患者[平均年龄(77±10)岁],其中多支冠脉病变(狭窄... 目的人工神经网络(ANN)已被应用于探测心肌灌注缺损和缺血。该研究的目的是比较最新1.1版本的ANN与最初1.0版本的诊断准确性。方法研究了106例冠状动脉(简称冠脉)造影阳性的患者[平均年龄(77±10)岁],其中多支冠脉病变(狭窄≥50%)者占52%,陈旧性心肌梗死患者占27%,行冠脉重建术者占30%。1.0和1.1版本的ANN已分别在瑞典(1 051例)和日本(1 001例)用于99Tcm-甲氧基异丁基异腈(MIBI)心肌灌注显像的诊断训练,计算其诊断当地患者负荷态心肌灌注缺损和缺血的可能性(0.0~1.0)。以相关专家的阅片结果作为"金标准",计算受试者工作特征(ROC)曲线下面积(AUC),比较2个版本ANN的诊断准确性。结果1.1和1.0版本的ANN诊断负荷态心肌灌注缺损的AUC分别为0.95和0.93(P=0.27),但1.1版本诊断心肌缺血的能力显著提高(P=0.005 5),其AUC为0.96(灵敏度87%,特异性96%),1.0版本的AUC为0.89(灵敏度78%,特异性97%)。在未行冠脉重建且无陈旧性心肌梗死的患者中,1.1版本的AUC也有显著提高(P=0.009 3),其AUC为0.98(灵敏度88%,特异性100%),而1.0版本的AUC为0.88(灵敏度76%,特异性100%)。与1.0版本相比,1.1版本的中位ANN可能性常为0.1~0.7,这使得1.1版本的诊断准确性更高。以冠脉狭窄作为"金标准"时,1.1版本的诊断准确性在单支冠脉病变或无冠脉狭窄的患者中也有提高(47例;AUC:0.81与0.66,P=0.006 0)。结论1.1版本的ANN在日本人数据库中训练后,其诊断能力得到提高,尤其在诊断心肌缺血方面。 展开更多
关键词 核心脏病学 人工智能 心肌灌注显像 冠状动脉粥样硬化性心脏病
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