NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE20506 Query DataSets for GSE20506
Status Public on Jun 02, 2010
Title Identification of cis- and trans-acting factors involved in the localization of MALAT-1 to nuclear speckles
Organism Homo sapiens
Experiment type Expression profiling by array
Summary MALAT-1 is a long mammalian non-coding transcript of approximately 8500 nucleotides. It is localized to nuclear speckles despite its mRNA-like characteristics, which usually result in the export of transcripts to the cytoplasm. In the present study, we report the identification of several factors that influence the nuclear speckle localization of MALAT-1, and we provide evidence that MALAT-1 is involved in the regulation of gene expression. Heterokaryon assays revealed that MALAT-1 does not shuttle between the nucleus and cytoplasm, but is stably retained within the nucleus. Analysis of MALAT-1 fragments showed that MALAT-1 contains two distinct nuclear speckle-directing elements (between nucleotides 1961 to 3040 and 6008 to 7011 of the MALAT-1 sequence). The knockdown of the nuclear speckle proteins, RNPS1, SRm160 or IBP160, resulted in the diffusion of MALAT-1 to the nucleoplasm. In addition, we have demonstrated that depletion of MALAT-1 represses the expression of several genes. This repression of gene expression also occurs in response to the delocalization of MALAT-1 from the nuclear speckles. These results suggest that RNPS1, SRm160 and IBP160 contribute to the localization of MALAT-1 to nuclear speckles where it is involved in regulating gene expression
 
Overall design We used DNA microarray analysis to analyze differentially expressed (up- and down-regulated) genes in cells depleted of MALAT-1 by RNAi. Microarray analysis using the Agilent Whole Human Genome 4 x 44K oligo microarray in two independent MALAT-1 knockdown cell lines transfected with different siRNAs. Total RNA (800 ng) was labeled with either Cy3 or Cy5 dye using an Agilent Low RNA Input Fluorescent Linear Amplification Kit (Agilent). Fluorescently labeled cRNAs, derived from total RNA isolated from control cells, and from MALAT-1 knockdown cells, were hybridized to the same microarray slide carrying 60-mer probes from the whole human genome 4 x 44K oligo microarray kit (Agilent Technologies, Palo Alto, CA, USA). A flip labeling (dye-swap or reverse labeling with Cy3 and Cy5 dyes) procedure was followed to nullify the dye bias associated with unequal incorporation of the two Cy dyes into cDNA.
 
Contributor(s) Miyagawa R, Mizuno R, Nakamura Y, Ijiri K, Rakwal R, Shibato J, Masuo Y, Hirose T, Akimitsu N
Citation(s) 20937273, 22355166
Submission date Feb 24, 2010
Last update date Feb 22, 2018
Contact name RANDEEP RAKWAL
E-mail(s) plantproteomics@gmail.com
Phone +81-(0)90-1853-7875
Organization name University of Tsukuba
Department Institute of Health and Sport Sciences
Lab GSI 403
Street address 1-1-1 Tennodai
City Tsukuba
State/province Ibaraki
ZIP/Postal code 305-8574
Country Japan
 
Platforms (1)
GPL4133 Agilent-014850 Whole Human Genome Microarray 4x44K G4112F (Feature Number version)
Samples (4)
GSM515253 HeLa_Control (Cy3)_HeLa_MALAT-1 (Cy5)_Replication 1
GSM515254 HeLa_Control (Cy5)_HeLa_MALAT-1 (Cy3)_Replication 1
GSM515255 HeLa_Control (Cy3)_HeLa_MALAT-1 (Cy5)_Replication 2
Relations
BioProject PRJNA125093

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE20506_RAW.tar 68.8 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap