Open AccessNucleotide Sequence and Secondary Structure of Citrus Exocortis and Chrysanthemum Stunt Viroid
Author(s) -
GROSS Hans J.,
KRUPP Guido,
DOMDEY Horst,
RABA Manfred,
JANK Peter,
LOSSOW Christine,
ALBERTY Heidemarie,
SÄNGER Heinz L.,
RAMM Karla
Publication year - 1982
Publication title -
european journal of biochemistry
Language(s) - English
Resource type - Journals
eISSN - 1432-1033
pISSN - 0014-2956
DOI - 10.1111/j.1432-1033.1982.tb05779.x
Subject(s) - viroid , biology , rna , nucleotide , nucleic acid sequence , potato spindle tuber viroid , base pair , homology (biology) , genetics , virology , dna , gene
The complete nucleotide sequence of citrus exocortis viroid (CEV, propagated in Gymura) and chrysanthemum stunt viroid (CSV, propagated in Cineraria) has been established, using labelling in vitro and direct RNA sequencing methods and a new screening procedure for the rapid selection of suitable RNA fragments from limited digests. The covalently closed circular single‐stranded viroid RNAs consist of 371 (CEV) and 354 (CSV) nucleotides, respectively. As previously shown for potato spindle tuber viroid (PSTV, 359 nucleotides), CEV and CSV also contain a long polypurine sequence. Maximal base‐pairing of the established CEV and CSV sequences results in an extended rod‐like secondary structure similar to that previously established for PSTV and as predicted from detailed physicochemical studies of all these viroids. Although the three viroid species sequenced to date differ in size and nucleotide sequence, there is 60–73% homology between them. As PSTV, CEV and CSV also contain conserved complementary sequences which are separated from each other in the native secondary structure. We postulate that the resulting ‘secondary’ hairpins, being formed and observed in vitro during the complex process of thermal denaturation of viroid RNA, must have a vital, although yet unknown, function in vivo . The possible origin and function of viroids are discussed on the basis of the characteristic structural features and of a considerable homology with Ula RNA found for a region highly conserved in the three viroids.