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Attila Molnar

Researcher at University of Edinburgh

Publications -  67
Citations -  6110

Attila Molnar is an academic researcher from University of Edinburgh. The author has contributed to research in topics: RNA silencing & RNA. The author has an hindex of 28, co-authored 58 publications receiving 5452 citations. Previous affiliations of Attila Molnar include John Innes Centre & Hungarian Academy of Sciences.

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Small Silencing RNAs in Plants Are Mobile and Direct Epigenetic Modification in Recipient Cells

TL;DR: In Arabidopsis, both exogenous and endogenous small interfering RNAs (siRNAs), rather than their long double-stranded precursor RNAs, are the molecules that transfer information between plant cells and represent a mechanism for transmitting the specification of epigenetic modification.
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A viral protein suppresses RNA silencing and binds silencing‐generated, 21‐ to 25‐nucleotide double‐stranded RNAs

TL;DR: It is proposed that the 19 kDa protein (p19) of tombusviruses is a potent silencing suppressor that prevents the spread of mobile silencing signal by sequestering the PTGS‐generated 21–25 nt dsRNAs, thus depleting the specificity determinants of PTGS effector complexes.
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miRNAs control gene expression in the single-cell alga Chlamydomonas reinhardtii

TL;DR: The unicellular alga Chlamydomonas reinhardtii is shown to contain miRNAs, putative evolutionary precursors of mi RNAs and species of siRNAs resembling those in higher plants, indicating that complex RNA-silencing systems evolved before multicellularity and were a feature of primitive eukaryotic cells.
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Low temperature inhibits RNA silencing-mediated defence by the control of siRNA generation

TL;DR: It is shown that in cold, plants become more susceptible to viruses, and RNA silencing‐based phenotypes of transgenic plants are lost, suggesting that the two classes of small RNAs are generated by different nuclease complexes.
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Plant Virus-Derived Small Interfering RNAs Originate Predominantly from Highly Structured Single-Stranded Viral RNAs

TL;DR: The results suggest that virus-derived siRNAs originate predominantly by direct DICER cleavage of imperfect duplexes in the most folded regions of the positive strand of the viral RNA.