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Insecticidal activity of three 10–12 nucleotides long antisense sequences from 5.8S ribosomal RNA gene of gypsy moth Lymantria dispar L. against its larvae

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Oberemok V. V. , Laikova K. V. , Useinov R. Z. , Gal’chinsky, Nikita V. , Novikov I. A. , Yurchenko K. A. , Volkov M. E. , Gorlov M. V. , Brailko V. A. , Plugatar Y. V. , Oberemok V. V. , Laikova K. V. , Useinov R. Z. , Gal’chinsky, Nikita V. , Novikov I. A. , Yurchenko K. A. , Volkov M. E. , Gorlov M. V. , Brailko V. A. , Plugatar Y. V.

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DNA insecticides: The effect of concentration on non-target plant organisms such as wheat (Triticum aestivum L.)

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Nyadar P. M. , Oberemok V. , Omelchenko A. , Kerimova S. , Seidosmanova E. , Krasnodubiets A. , Shumskykh M. , Bekirova V.

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A breakthrough in the efficiency of contact DNA insecticides: rapid high mortality rates in the sap-sucking insects Dynaspidiotus britannicus Comstock and Unaspis euonymi Newstead

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Gal’chinsky, Nikita , Useinov R. , Yatskova E. , Laikova K. , Novikov I. , Gorlov M. , Trikoz N. , Sharmagiy A. , Plugatar Y. , Oberemok V. , Gal’chinsky, Nikita , Useinov R. , Yatskova E. , Laikova K. , Novikov I. , Gorlov M. , Trikoz N. , Sharmagiy A. , Plugatar Y. , Oberemok V.

Synteza modyfikowanych oligonukleotydów zawierających stereozdefiniowane internukleotydowe wiązania tiofosforanowe

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Radzikowska E. , Kaczmarek R. , Baraniak J.

tom [Z] 69, 11-12

957--981

Synthetic oligonucleotides constitute an important class of compounds which can exhibit biological activity. As potential drugs they could be employed in antisense strategy by acting on the pathogenic mRNA, causing inactivation of the target molecules during the translation process [1]. Ideal antisense agent (ASO) should be resistant to exo and/or endonucleases, exhibit a suitable pharmacological and pharmacokinetic profile and exhibits high binding affinity towards the target mRNA. To improve some properties of the ASO plethora of the chemical modifications introduced within the nucleobase, sugar unit and internucleotide linkage are investigated [3]. Among them, phosphorothioate oligonucleotides (PS-oligo), created by replacing one of the nonbridging oxygen atoms with a sulfur atom, are the major representatives of DNA analogs. PS-oligo display several attractive features like nuclease resistance, activation of RNase H, and good pharmacokinetic properties [1]. Replacement of one of two nonbridging oxygens at phosphorus by sulfur induces asymmetry at the phosphorus atom. Hence, the synthesized oligo(nucleoside phosphorothioate) is a mixture of 2n diastereomers (where n is the number of internucleotide phosphorothioate functions). Therefore the actual biological activity of the P-chiral oligonucleotide analogues, (e.g., interactions with proteins or nucleic acids) may depend on stereochemical factors [7]. One has to keep in mind that the phosphoramidite [5] and H-phosphonate [32] methodologies (commonly used to prepare PS-oligo) are nonstereospecific and give a mixture of 2n diastereomers. Thus, various methods have been elaborated to synthesize these P-chiral oligonucleotide analogs in a stereocontrolled manner [15, 17], among them the oxathiaphospholane method developed by Stec et al. [18], the method utilizing nucleoside 3’-O-(3-N-acyl)oxazaphospholidine derivatives as monomer units [19], and the method based on a stereoselective synthesis of nucleoside 3’-O-oxazaphospholidine monomers [21, 22] are the most significant.