Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (81)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Nemes, J. P.
Right arrow Articles by Koob, M. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nemes, J. P.
Right arrow Articles by Koob, M. D.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Molecular Genetics, 2000, Vol. 9, No. 10 1543-1551
© 2000 Oxford University Press

The SCA8 transcript is an antisense RNA to a brain-specific transcript encoding a novel actin-binding protein (KLHL1)

Jozsef P. Nemes, Kellie A. Benzow and Michael D. Koob+

Department of Neurology and Institute of Human Genetics, Box 206 UMHC, 420 Delaware Street SE, University of Minnesota, Minneapolis, MN 55455, USA.

Spinocerebellar ataxia type 8 (SCA8) is a neurodegenerative disorder caused by the expansion of a CTG trinucleotide repeat that is transcribed as part of an untranslated RNA. As a step towards understanding the molecular pathology of SCA8, we have defined the genomic organization of the SCA8 RNA transcripts and assembled a 166 kb segment of genomic sequence containing the repeat. The most striking feature of the SCA8 transcripts is that the most 5' exon is transcribed through the first exon of another gene that is transcribed in the opposite orientation. This gene arrangement suggests that the SCA8 transcript is an endogenous antisense RNA that overlaps the transcription and translation start sites as well as the first splice donor sequence of the sense gene. The sense transcript encodes a 748 amino acid protein with a predicted domain structure typical of a family of actin-organizing proteins related to the Drosophila Kelch gene, and so has been given the name Kelch-like 1 (KLHL1). We have identified the full-length cDNA sequence for both the human and mouse KLHLI genes, and have elucidated the general genomic organization of the human gene. The predicted open reading frame and promoter region are highly conserved, and both genes are primarily expressed in specific brain tissues, including the cerebellum, the tissue most affected by SCA8. Transfection studies with epitope-tagged KLHL1 demonstrate that the protein localizes to the cytoplasm, suggesting that it may play a role in organizing the actin cytoskeleton of the brain cells in which it is expressed.

+ To whom correspondence should be addressed. Tel: +1 612 626 4521; Fax: +1 612 626 2600;Email: koobx001@gold.tc.umn.edu


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
DevelopmentHome page
F. M. J. Jacobs, A. J. A. van der Linden, Y. Wang, L. von Oerthel, H. S. Sul, J. P. H. Burbach, and M. P. Smidt
Identification of Dlk1, Ptpru and Klhl1 as novel Nurr1 target genes in meso-diencephalic dopamine neurons
Development, July 15, 2009; 136(14): 2363 - 2373.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
O. A. Sofola, P. Jin, J. Botas, and D. L. Nelson
Argonaute-2-dependent rescue of a Drosophila model of FXTAS by FRAXE premutation repeat
Hum. Mol. Genet., October 1, 2007; 16(19): 2326 - 2332.
[Abstract] [Full Text] [PDF]


Home page
Physiol. Rev.Home page
M. F. Mehler and J. S. Mattick
Noncoding RNAs and RNA Editing in Brain Development, Functional Diversification, and Neurological Disease
Physiol Rev, July 1, 2007; 87(3): 799 - 823.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. Jiang, S. Seng, H. K. Avraham, Y. Fu, and S. Avraham
Process Elongation of Oligodendrocytes Is Promoted by the Kelch-related Protein MRP2/KLHL1
J. Biol. Chem., April 20, 2007; 282(16): 12319 - 12329.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
K. V. Prasanth and D. L. Spector
Eukaryotic regulatory RNAs: an answer to the 'genome complexity' conundrum
Genes & Dev., January 1, 2007; 21(1): 11 - 42.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
S. Seng, H. K. Avraham, S. Jiang, S. Venkatesh, and S. Avraham
KLHL1/MRP2 Mediates Neurite Outgrowth in a Glycogen Synthase Kinase 3{beta}-Dependent Manner
Mol. Cell. Biol., November 15, 2006; 26(22): 8371 - 8384.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
Y. He, T. Zu, K. A. Benzow, H. T. Orr, H. B. Clark, and M. D. Koob
Targeted Deletion of a Single Sca8 Ataxia Locus Allele in Mice Causes Abnormal Gait, Progressive Loss of Motor Coordination, and Purkinje Cell Dendritic Deficits
J. Neurosci., September 27, 2006; 26(39): 9975 - 9982.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
M. F. Mehler and J. S. Mattick
Non-coding RNAs in the nervous system
J. Physiol., September 1, 2006; 575(2): 333 - 341.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
M. Wakamiya, T. Matsuura, Y. Liu, G. C. Schuster, R. Gao, W. Xu, P. S. Sarkar, X. Lin, and T. Ashizawa
The role of ataxin 10 in the pathogenesis of spinocerebellar ataxia type 10
Neurology, August 22, 2006; 67(4): 607 - 613.
[Abstract] [Full Text] [PDF]


Home page
Genes Dev.Home page
J. Feng, C. Bi, B. S. Clark, R. Mady, P. Shah, and J. D. Kohtz
The Evf-2 noncoding RNA is transcribed from the Dlx-5/6 ultraconserved region and functions as a Dlx-2 transcriptional coactivator
Genes & Dev., June 1, 2006; 20(11): 1470 - 1484.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
K. C. Pang, S. Stephen, P. G. Engstrom, K. Tajul-Arifin, W. Chen, C. Wahlestedt, B. Lenhard, Y. Hayashizaki, and J. S. Mattick
RNAdb--a comprehensive mammalian noncoding RNA database
Nucleic Acids Res., January 1, 2005; 33(suppl_1): D125 - D130.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
C. M. Everett and N. W. Wood
Trinucleotide repeats and neurodegenerative disease
Brain, November 1, 2004; 127(11): 2385 - 2405.
[Abstract] [Full Text] [PDF]


Home page
J. Neurol. Neurosurg. PsychiatryHome page
A Zeman, J Stone, M Porteous, E Burns, L Barron, and J Warner
Spinocerebellar ataxia type 8 in Scotland: genetic and clinical features in seven unrelated cases and a review of published reports
J. Neurol. Neurosurg. Psychiatry, March 1, 2004; 75(3): 459 - 465.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
D. Nolte, S. Niemann, and U. Muller
Specific sequence changes in multiple transcript system DYT3 are associated with X-linked dystonia parkinsonism
PNAS, September 2, 2003; 100(18): 10347 - 10352.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
B.P.C. van de Warrenburg, R.J. Sinke, C.C. Verschuuren-Bemelmans, H. Scheffer, E.R. Brunt, P.F. Ippel, J.A. Maat-Kievit, D. Dooijes, N.C. Notermans, D. Lindhout, et al.
Spinocerebellar ataxias in the Netherlands: Prevalence and age at onset variance analysis
Neurology, March 12, 2002; 58(5): 702 - 708.
[Abstract] [Full Text] [PDF]


Home page
Arch NeurolHome page
E. Cellini, B. Nacmias, P. Forleo, S. Piacentini, B. M. Guarnieri, A. Serio, A. Calabro, D. Renzi, and S. Sorbi
Genetic and Clinical Analysis of Spinocerebellar Ataxia Type 8 Repeat Expansion in Italy
Arch Neurol, November 1, 2001; 58(11): 1856 - 1859.
[Abstract] [Full Text] [PDF]


Home page
Mol Biol EvolHome page
J. S. Mattick and M. J. Gagen
Review ArticleThe Evolution of Controlled Multitasked Gene Networks: The Role of Introns and Other Noncoding RNAs in the Development of Complex Organisms
Mol. Biol. Evol., September 1, 2001; 18(9): 1611 - 1630.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
V. A. Erdmann, M. Z. Barciszewska, M. Szymanski, A. Hochberg, N. d. Groot, and J. Barciszewski
The non-coding RNAs as riboregulators
Nucleic Acids Res., January 1, 2001; 29(1): 189 - 193.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.