scholarly journals The Characterization of microRNA-Mediated Gene Regulation as Impacted by Both Target Site Location and Seed Match Type

PLoS ONE ◽  
2014 ◽  
Vol 9 (9) ◽  
pp. e108260 ◽  
Author(s):  
Wenlong Xu ◽  
Zixing Wang ◽  
Yin Liu
1986 ◽  
Vol 6 (3) ◽  
pp. 933-941
Author(s):  
J E Garrett ◽  
D Carroll

A family of transposable genetic elements in the genome of the frog, Xenopus laevis, is described. They are designated Tx1. Transposability of the elements was deduced by characterization of a chromosomal locus which is polymorphic for the presence or absence of a Tx1 element. Nucleotide sequence analysis suggested that Tx1 elements show target site specificity, as they are inserted at the pentanucleotide TTTAA in all four cases that were examined. The elements appear to have 19-base-pair (bp) inverted terminal repeats, and they are flanked by 4-bp target duplications (TTAA), although the possibility that they do not create target site duplications is discussed. Tx1 elements have several unusual characteristics: the central portion of each element is comprised of a variable number of two types of 393-bp repeating units; the rightmost 1,000 bp of the element contains separate regions potentially capable of forming bends, left-handed Z-form DNA, and alternative stem-loop structures. Comparisons among single frogs suggest that germ line transposition is relatively infrequent and that variations in numbers of internal repeats accumulate quite slowly at any locus.


Author(s):  
R.D. Wells ◽  
T. Goodman ◽  
S. Hardies ◽  
W. Hillen ◽  
G. Horn ◽  
...  

2005 ◽  
Vol 49 (1) ◽  
pp. 441-443 ◽  
Author(s):  
J. Gangoue-Pieboji ◽  
V. Miriagou ◽  
S. Vourli ◽  
E. Tzelepi ◽  
P. Ngassam ◽  
...  

ABSTRACT CTX-M-15-producing Klebsiella pneumoniae and Escherichia coli emerged recently in Cameroon. CTX-M-15 was encoded by two different multiresistance plasmids, of which one carried an ISEcp1-bla CTX-M-15 element flanked by a 5-bp target site duplication and inserted within a Tn2-derived sequence. A truncated form of this element in the second plasmid was identified.


2005 ◽  
Vol 33 (1) ◽  
pp. 33-35 ◽  
Author(s):  
B. Brito ◽  
C. Baginsky ◽  
J.M. Palacios ◽  
E. Cabrera ◽  
T. Ruiz-Argüeso ◽  
...  

Uptake hydrogenases in legume endosymbiotic bacteria recycle hydrogen produced during the nitrogen fixation process in legume nodules. Despite the described beneficial effect on plant productivity, the hydrogen oxidation capability is not widespread in the Rhizobiaceae family. Characterization of hydrogenase gene clusters in strains belonging to Rhizobium, Bradyrhizobium and Azorhizobium reveals a similar overall genetic organization along with important differences in gene regulation. In addition, phylogenetic analysis of hup genes indicates distinct evolutionary origins for hydrogenase genes in Rhizobia.


2011 ◽  
Vol 55 (11) ◽  
pp. 5370-5373 ◽  
Author(s):  
Gaelle Cuzon ◽  
Thierry Naas ◽  
Patrice Nordmann

ABSTRACTThe carbapenemase geneblaKPC, which is rapidly spreading worldwide, is located on a Tn3-based transposon, Tn4401. In a transposition-conjugation assay, Tn4401was able to mobilizeblaKPC-2gene at a frequency of 4.4 × 10−6/recipient cell. A 5-bp target site duplication was evidenced upon each insertion without target site specificity. This study demonstrated that Tn4401is an active transposon capable of mobilizingblaKPCgenes at high frequency.


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