Locally-Resolved Study of Degradation in a SOFC Repeat-Element

2019 ◽  
Vol 25 (2) ◽  
pp. 457-466 ◽  
Author(s):  
Zacharie Wuillemin ◽  
Arata Nakajo ◽  
Andres Müller ◽  
Andreas J. Schuler ◽  
Stefan Diethelm ◽  
...  
Keyword(s):  

1995 ◽  
Vol 4 (2) ◽  
pp. 253-256 ◽  
Author(s):  
Henry F. Oettinger ◽  
Amelie Rodrigue-Way ◽  
Joyce J. Bousquet ◽  
Albert S.B. Edge

Using a digoxygenin-labelled DNA probe derived from the porcine repeat element PRE-1, we have developed a protocol for the detection of transplanted porcine islets and hepatocytes against a background of murine host tissue. Analysis of this probe by Southern blotting indicated that PRE-1 hybridizes to pig genomic DNA but not to human or mouse DNA. On tissue sections, hybridizing probe was detected using alkaline phosphatase-conjugated anti-digoxygenin antibody visualized with 5-bromo-4-chloro-3-indolyl-phosphate/4-nitro-blue tetrazolium chloride (BCIP/ NBT) substrate. We have demonstrated sensitive and highly specific staining of porcine nuclei in fixed, paraffin embedded tissue sections, and have applied the technique to detect porcine pancreatic islets and hepatocytes transplanted into murine kidney and spleen. Applications of this technique include detection of transplanted cells or organs across a variety of xenogeneic barriers.





2009 ◽  
Vol 90 (6) ◽  
pp. 1505-1514 ◽  
Author(s):  
Asieh Rasoolizadeh ◽  
Catherine Béliveau ◽  
Don Stewart ◽  
Conrad Cloutier ◽  
Michel Cusson

The endoparasitic wasp Tranosema rostrale transmits an ichnovirus to its lepidopteran host, Choristoneura fumiferana, during parasitization. As shown for other ichnoviruses, the segmented dsDNA genome of the T. rostrale ichnovirus (TrIV) features several multi-gene families, including the repeat element (rep) family, whose products display no known similarity to non-ichnovirus proteins, except for a homologue encoded by the genome of the Helicoverpa armigera granulovirus; their functions remain unknown. This study applied linear regression of efficiency analysis to real-time PCR quantification of transcript abundance for all 17 TrIV rep open reading frames (ORFs) in parasitized and virus-injected C. fumiferana larvae, as well as in T. rostrale ovaries and head–thorax complexes. Although transcripts were detected for most rep ORFs in infected caterpillars, two of them clearly outnumbered the others in whole larvae, with a tendency for levels to drop over time after infection. The genome segments bearing the three most highly expressed rep genes in parasitized caterpillars were present in higher proportions than other rep-bearing genome segments in TrIV DNA, suggesting a possible role for gene dosage in the regulation of transcription level. TrIV rep genes also showed important differences in the relative abundance of their transcripts in specific tissues (cuticular epithelium, the fat body, haemocytes and the midgut), implying tissue-specific roles for individual members of this gene family. Significantly, no rep transcripts were detected in T. rostrale head–thorax complexes, whereas some were abundant in ovaries. There, the transcription pattern was completely different from that observed in infected caterpillars, suggesting that some rep genes have wasp-specific functions.



1990 ◽  
Vol 1 (1) ◽  
pp. 79-93 ◽  
Author(s):  
Eric M. Hallerman ◽  
John F. Schneider ◽  
Mark Gross ◽  
Zhanjiang Liu ◽  
Sung Joo Yoon ◽  
...  


2008 ◽  
Vol 6 (7) ◽  
pp. 1183-1190 ◽  
Author(s):  
C. HOUGH ◽  
C. L. CAMERON ◽  
C. R. P. NOTLEY ◽  
C. BROWN ◽  
L. O’BRIEN ◽  
...  


2013 ◽  
Vol 54 (3-4) ◽  
pp. 254-263 ◽  
Author(s):  
Prachi Dongre ◽  
Stephen Mathew ◽  
Irina Akopova ◽  
Ignacy Gryczynski ◽  
Porunelloor Mathew
Keyword(s):  


1984 ◽  
Vol 81 (15) ◽  
pp. 4617-4621 ◽  
Author(s):  
J. Sodroski ◽  
M. Trus ◽  
D. Perkins ◽  
R. Patarca ◽  
F. Wong-Staal ◽  
...  


Genome ◽  
1995 ◽  
Vol 38 (6) ◽  
pp. 1132-1138 ◽  
Author(s):  
T. E. Broad ◽  
P. E. Lewis ◽  
P. D. Pearce ◽  
S. H. Phua ◽  
J. W. Forrest ◽  
...  

A DNA repeat element, revealed initially by digestion of horse DNA with TaqI, was cloned and characterized by Southern and in situ hybridization studies and nucleotide sequencing. The clone, e4/1, consisted of 32 tandem reiterations of a unit repeat of 21–22 bp, and produced multilocus DNA fingerprinting profiles that were useful for parentage analysis in horses. The tandem repeat element was shown by in situ hybridization to be localized in the centromeres of the acrocentric but not metacentric classes of horse chromosomes.Key words: Equidae, Equus caballus, DNA repeat, DNA fingerprinting, centromere.





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