Cloning and functional characterization of BcatrA, a gene encoding an ABC transporter of the plant pathogenic fungus Botryotinia fuckeliana (Botrytis cinerea)

2008 ◽  
Vol 112 (6) ◽  
pp. 737-746 ◽  
Author(s):  
Giovanni Del Sorbo ◽  
Michelina Ruocco ◽  
Henk-jan Schoonbeek ◽  
Felice Scala ◽  
Catello Pane ◽  
...  
2020 ◽  
Vol 165 (4) ◽  
pp. 1033-1037 ◽  
Author(s):  
Wenyi Liu ◽  
Du Hai ◽  
Fan Mu ◽  
Xiaojing Yu ◽  
Yingtong Zhao ◽  
...  

Gene ◽  
2006 ◽  
Vol 376 (1) ◽  
pp. 59-67 ◽  
Author(s):  
Sandra Morales-Arrieta ◽  
Maria Elena Rodríguez ◽  
Lorenzo Segovia ◽  
Agustín López-Munguía ◽  
Clarita Olvera-Carranza

2014 ◽  
Vol 28 (S1) ◽  
Author(s):  
Jonas Lee ◽  
Janet Yang ◽  
Daniel Zhitnitsky ◽  
Oded Lewinson ◽  
Douglas Rees

Virology ◽  
2016 ◽  
Vol 489 ◽  
pp. 86-94 ◽  
Author(s):  
Pengfei Li ◽  
Yanhong Lin ◽  
Hailong Zhang ◽  
Shuangchao Wang ◽  
Dewen Qiu ◽  
...  

1998 ◽  
Vol 44 (1) ◽  
pp. 91-94
Author(s):  
G Scott Jenkins ◽  
Mark S Chandler ◽  
Pamela S Fink

The putative 4.5S RNA of Haemophilus influenzae was identified in the genome by computer analysis, amplified by the polymerase chain reaction, and cloned. We have determined that this putative 4.5S RNA will complement an Escherichia coli strain conditionally defective in 4.5S RNA production. The predicted secondary structures of the molecules were quite similar, but Northern analysis showed that the H. influenzae RNA was slightly larger than the E. coli RNA. The H. influenzae gene encoding this RNA is the functional homolog of the ffs gene in E. coli. Key words: ffs gene, complementation studies, small RNA, prokaryotic genetics.


2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Stefanie Scheiper-Welling ◽  
Paolo Zuccolini ◽  
Oliver Rauh ◽  
Britt-Maria Beckmann ◽  
Christof Geisen ◽  
...  

Abstract Background Alterations in the SCN5A gene encoding the cardiac sodium channel Nav1.5 have been linked to a number of arrhythmia syndromes and diseases including long-QT syndrome (LQTS), Brugada syndrome (BrS) and dilative cardiomyopathy (DCM), which may predispose to fatal arrhythmias and sudden death. We identified the heterozygous variant c.316A > G, p.(Ser106Gly) in a 35-year-old patient with survived cardiac arrest. In the present study, we aimed to investigate the functional impact of the variant to clarify the medical relevance. Methods Mutant as well as wild type GFP tagged Nav1.5 channels were expressed in HEK293 cells. We performed functional characterization experiments using patch-clamp technique. Results Electrophysiological measurements indicated, that the detected missense variant alters Nav1.5 channel functionality leading to a gain-of-function effect. Cells expressing S106G channels show an increase in Nav1.5 current over the entire voltage window. Conclusion The results support the assumption that the detected sequence aberration alters Nav1.5 channel function and may predispose to cardiac arrhythmias and sudden cardiac death.


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