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Neuronal BC1 RNA structure: Evolutionary conversion of a tRNAAla domain into an extended stem-loop structure

Published online by Cambridge University Press:  04 May 2001

TIMOFEY S. ROZHDESTVENSKY
Affiliation:
Institute of Experimental Pathology/Molecular Neurobiology, D-48149 Münster, Germany Chemistry Department, Moscow State University, 119899, Moscow, Russian Federation
ALEXEI M. KOPYLOV
Affiliation:
Chemistry Department, Moscow State University, 119899, Moscow, Russian Federation
JÜRGEN BROSIUS
Affiliation:
Institute of Experimental Pathology/Molecular Neurobiology, D-48149 Münster, Germany
ALEXANDER HÜTTENHOFER
Affiliation:
Institute of Experimental Pathology/Molecular Neurobiology, D-48149 Münster, Germany
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Abstract

By chemical and enzymatic probing, we have analyzed the secondary structure of rodent BC1 RNA, a small brain-specific non-messenger RNA. BC1 RNA is specifically transported into dendrites of neuronal cells, where it is proposed to play a role in regulation of translation near synapses. In this study we demonstrate that the 5′ domain of BC1 RNA, derived from tRNAAla, does not fold into the predicted canonical tRNA cloverleaf structure. We present evidence that by changing bases within the tRNAAla domain during the course of evolution, an extended stem-loop structure has been created in BC1 RNA. The new structural domain might function, in part, as a putative binding site for protein(s) involved in dendritic transport of BC1 RNA within neurons. Furthermore, BC1 RNA contains, in addition to the extended stem-loop structure, an internal poly(A)-rich region that is supposedly single stranded, followed by a second smaller stem-loop structure at the 3′ end of the RNA. The three distinct structural domains reflect evolutionary legacies of BC1 RNA.

Type
Research Article
Copyright
2001 RNA Society

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