scholarly journals Nucleotide Analogues as Probes for DNA and RNA Polymerases

Author(s):  
Robert D. Kuchta
1991 ◽  
Vol 20 (3) ◽  
pp. 225-237 ◽  
Author(s):  
Benedict Shiu-Shing Chan ◽  
Deborah A. Court ◽  
P. John Vierula ◽  
Helmut Bertrand
Keyword(s):  

1995 ◽  
Vol 5 (1) ◽  
pp. 27-38 ◽  
Author(s):  
Edward Arnold ◽  
Jianping Ding ◽  
Stephen H. Hughes ◽  
Zdenek Hostomsky

1990 ◽  
Vol 190 (3) ◽  
pp. 469-476 ◽  
Author(s):  
Katsuhiko ONO ◽  
Hideo NAKANE ◽  
Masanori FUKUSHIMA ◽  
Jean-Claude CHERMANN ◽  
Francoise BARRE-SINOUSSI

2014 ◽  
Vol 38 (8) ◽  
pp. 940-947 ◽  
Author(s):  
Zhijian Wang ◽  
Fei Xu ◽  
Na Yuan ◽  
Yuna Niu ◽  
Weiwei Lin ◽  
...  

Author(s):  
David Bensimon ◽  
Vincent Croquette ◽  
Jean-François Allemand ◽  
Xavier Michalet ◽  
Terence Strick

This book presents a comprehensive overview of the foundations of single-molecule studies, based on manipulation of the molecules and observation of these with fluorescent probes. It first discusses the forces present at the single-molecule scale, the methods to manipulate them, and their pros and cons. It goes on to present an introduction to single-molecule fluorescent studies based on a quantum description of absorption and emission of radiation due to Einstein. Various considerations in the study of single molecules are introduced (including signal to noise, non-radiative decay, triplet states, etc.) and some novel super-resolution methods are sketched. The elastic and dynamic properties of polymers, their relation to experiments on DNA and RNA, and the structural transitions observed in those molecules upon stretching, twisting, and unzipping are presented. The use of these single-molecule approaches for the investigation of DNA–protein interactions is highlighted via the study of DNA and RNA polymerases, helicases, and topoisomerases. Beyond the confirmation of expected mechanisms (e.g., the relaxation of DNA torsion by topoisomerases in quantized steps) and the discovery of unexpected ones (e.g., strand-switching by helicases, DNA scrunching by RNA polymerases, and chiral discrimination by bacterial topoII), these approaches have also fostered novel (third generation) sequencing technologies.


1986 ◽  
Vol 80 (1) ◽  
pp. 171-180
Author(s):  
M.L. Ferrero ◽  
C. De la Torre

8-Hydroxyquinoline (HQ) chelates Mg2+ and Mn2+ and, secondarily, affects the activities of DNA and RNA polymerases. The in vivo effect of HQ has been estimated in Allium cepa L. meristems growing under new growth kinetics in the presence of this agent. HQ (at both 5 X 10(−5) M and 10(−4) M) depressed incorporation of [3H]uridine much more effectively than that of [3H]-thymidine. Cycle kinetics in meristems behaved as if they were independent of the rates of synthesis or accumulation of RNA since, under HQ, cycle time was only moderately modified and the new cycle kinetics achieved could be explained by the new rates of [3H]thymidine incorporation. Lengthened S periods were partially compensated for by shortened G2 phases, suggesting that, in these cells, both the growth cycle and its coupling with the DNA-division cycle were not disturbed by a decreased amount of RNA. Finally, the nucleolar cycle during mitosis, but not the interphase nucleolus, was modified under the new rates of RNA synthesis.


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