scholarly journals Apoptosis Gene Hunting Using Retroviral Expression Cloning: Identification of Vacuolar ATPase Subunit E

2003 ◽  
Vol 3 ◽  
pp. 51-58 ◽  
Author(s):  
Claire L. Anderson ◽  
Gwyn T. Williams

Over the past 10-15 years there has been an explosion of interest in apoptosis. The delayed realisation that cell death is an essential part of life for any multicellular organism has meant that, despite the recent and rapid developments of the last decade, the precise biochemical pathways involved in apoptosis remain incomplete and potentially novel genes may, as yet, remain undiscovered. The hunt is therefore on to bridge the remaining gaps in our knowledge. Our contribution to this research effort utilises a functional cloning approach to isolate important regulatory genes involved in apoptosis. This mini-review focuses on the use and advantages of a retroviral expression cloning strategy and describes the isolation and identification of one such potential apoptosis regulatory gene, namely that encoding vacuolar ATPase subunit E.

2001 ◽  
Vol 1 (S3) ◽  
pp. 33-33
Author(s):  
Claire L. Anderson ◽  
Gwyn T. Williams

2001 ◽  
Vol 1 ◽  
pp. 33-33
Author(s):  
Claire L. Anderson ◽  
Gwyn T. Williams

2014 ◽  
pp. 259-269 ◽  
Author(s):  
Vladislava Soso ◽  
Marija Skrinjar ◽  
Nevena Blagojev ◽  
Slavica Veskovic-Moracanin

As the aflatoxins represent a health-risk for humans because of their proven carcinogenicity, food-borne fungi that produce them as secondary metabolites, mainly Aspergillus flavus and Aspergillus parasiticus, have to be isolated and identified. The best argument for identifying problem fungi is that it indicates control points within the food system as part of a hazard analysis critical control point (HACCP) approach. This assumes there is a close link between fungus and toxin. Conventional methods for isolation and identification of fungi are time consuming and require admirably dedicated taxonomists. Hence, it is imperative to develop methodologies that are relatively rapid, highly specific and as an alternative to the existing methods. The polymerase chain reaction (PCR) facilitates the in vitro amplification of the target sequence. The main advantages of PCR is that organisms need not be cultured, at least not for a long time, prior to their detection, target DNA can be detected even in a complex mixture, no radioactive probes are required, it is rapid, sensitive and highly versatile. The gene afl-2 has been isolated and shown to regulate aflatoxin biosynthesis in A. flavus. Also, the PCR reaction was targeted against aflatoxin synthesis regulatory gene (aflR1) since these genes are nearly identical in A. flavus and A. parasiticus in order to indicate the possibility of detection of both the species with the same PCR system (primers/reaction). [Projekat Ministarstva nauke Republike Srbije, br. III46009] <br><br><font color="red"><b> This article has been retracted. Link to the retraction <u><a href="http://dx.doi.org/10.2298/APT1647265E">10.2298/APT1647265E</a><u></b></font>


2013 ◽  
Author(s):  
Gajendra K. Katara ◽  
Mukesh K. Jaiswal ◽  
Alice Gilmam-Sacks ◽  
Kenneth D. Beaman

1994 ◽  
Vol 1190 (1) ◽  
pp. 193-196 ◽  
Author(s):  
Ralph Gräf ◽  
William R. Harvey ◽  
Helmut Wieczorek

2004 ◽  
Vol 41 (1) ◽  
pp. 125-132 ◽  
Author(s):  
Georg Strompen ◽  
Jan Dettmer ◽  
York-Dieter Stierhof ◽  
Karin Schumacher ◽  
Gerd Jürgens ◽  
...  

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