Nucleic Acids Research, 2003, Vol. 31, No. 19 5463-5468
© 2003 Oxford University Press
Structures of trinucleotide repeats in human transcripts and their functional implications
Laboratory of Cancer Genetics, Institute of Bioorganic Chemistry, Polish Academy of Sciences, Noskowskiego 12/14 St, 61-704, Poznan, Poland
*To whom correspondence should be addressed. Tel: +48 61 8528503; Fax: +48 61 8520532; Email: wlodkrzy{at}ibch.poznan.pl
Present address:
Marek Napierala, Institute of Biosciences and Technology, Center for Genome Research, Texas A&M University System Health Science Center, Texas Medical Center, Houston, TX 77030-3303, USA
Among the goals of RNA structural and functional genomics is determining structures and establishing the functions of a rich repertoire of simple sequence repeats in transcripts. These repeats are present in transcripts from their birth in the nucleus to their death in cytoplasm and have the potential of being involved in many steps of RNA regulation. The knowledge of their structural features and functional roles will also shed more light on the postulated mechanisms of RNA pathogenesis in a growing list of neurological diseases caused by simple sequence repeat expansions. Here, we discuss several different lines of research to support the hypothesis that the mechanism of RNA pathogenesis may be a more common phenomenon triggered or modulated also by abundant long normal repeats. We propose structures of the repeat regions in transcripts of genes involved in Triplet Repeat Expansion Diseases. We have classified the polymorphic repeat alleles of these genes according to their ability to form hairpin structures in transcripts, and describe the distribution of different structural forms of the repeats in the human population. We have also reported the results of a systematic survey of the human transcriptome to identify mRNAs containing triplet repeats and to classify them according to structural and functional criteria. Based on this knowledge, we discuss the putative wider role of triplet repeat RNA hairpins in human diseases. A hypothetical model is proposed in which long normal RNA hairpins formed by the repeats may also be involved in pathogenesis.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
M. Molla, A. Delcher, S. Sunyaev, C. Cantor, and S. Kasif Triplet repeat length bias and variation in the human transcriptome PNAS, October 6, 2009; 106(40): 17095 - 17100. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Kiliszek, R. Kierzek, W. J. Krzyzosiak, and W. Rypniewski Structural insights into CUG repeats containing the 'stretched U-U wobble': implications for myotonic dystrophy Nucleic Acids Res., July 1, 2009; 37(12): 4149 - 4156. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Holt, V. Jacquemin, M. Fardaei, C. A. Sewry, G. S. Butler-Browne, D. Furling, J. D. Brook, and G. E. Morris Muscleblind-Like Proteins: Similarities and Differences in Normal and Myotonic Dystrophy Muscle Am. J. Pathol., January 1, 2009; 174(1): 216 - 227. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Khateb, P. Weisman-Shomer, I. Hershco-Shani, A. L. Ludwig, and M. Fry The tetraplex (CGG)n destabilizing proteins hnRNP A2 and CBF-A enhance the in vivo translation of fragile X premutation mRNA Nucleic Acids Res., September 27, 2007; 35(17): 5775 - 5788. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Holt, S. Mittal, D. Furling, G. S Butler-Browne, J. D. Brook, and G. E. Morris Defective mRNA in myotonic dystrophy accumulates at the periphery of nuclear splicing speckles Genes Cells, September 1, 2007; 12(9): 1035 - 1048. [Abstract] [Full Text] [PDF] |
||||
![]() |
K B Lundin, Y L Giwercman, L Rylander, L Hagmar, and A Giwercman Androgen receptor gene GGN repeat length and reproductive characteristics in young Swedish men. Eur. J. Endocrinol., August 1, 2006; 155(2): 347 - 354. [Abstract] [Full Text] [PDF] |
||||
![]() |
K.A. Freed, D.W. Cooper, S.P. Brennecke, and E.K. Moses Detection of CAG repeats in pre-eclampsia/eclampsia using the repeat expansion detection method Mol. Hum. Reprod., July 1, 2005; 11(7): 481 - 487. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Sobczak and W. J. Krzyzosiak CAG Repeats Containing CAA Interruptions Form Branched Hairpin Structures in Spinocerebellar Ataxia Type 2 Transcripts J. Biol. Chem., February 4, 2005; 280(5): 3898 - 3910. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Sobczak and W. J. Krzyzosiak Imperfect CAG Repeats Form Diverse Structures in SCA1 Transcripts J. Biol. Chem., October 1, 2004; 279(40): 41563 - 41572. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Sobczak, M. de Mezer, G. Michlewski, J. Krol, and W. J. Krzyzosiak RNA structure of trinucleotide repeats associated with human neurological diseases Nucleic Acids Res., October 1, 2003; 31(19): 5469 - 5482. [Abstract] [Full Text] [PDF] |
||||






