NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE176304 Query DataSets for GSE176304
Status Public on Jul 09, 2021
Title Expression and Function of C1orf132 Long-Noncoding RNA in Breast Cancer Cell Lines and Tissues
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary miR-29b2 and miR-29c play a suppressive role in breast cancer progression. C1orf132 (also named MIR29B2CHG) is the host gene for generating both microRNAs. However, the region also expresses longer transcripts with unknown function. We employed bioinformatics and experi-mental approaches to decipher C1orf132 expression and function in breast cancer tissues. We also used the CRISPR/Cas9 technique to excise a predicted C1orf132 distal promoter and followed the behavior of the edited cells by real-time PCR, flow cytometry, migration assay, and RNA-seq tech-niques. We observed that C1orf132 long transcript is significantly downregulated in tri-ple-negative breast cancer. We also identified a promoter for the longer transcripts of C1orf132 whose functionality was demonstrated by transfecting MCF7 cells with a C1orf132 promoter-GFP construct. Knocking-out the promoter by means of CRISPR/Cas9 revealed no expression alteration of the neighboring genes CD46 and CD34, while the expression of miR-29c was reduced by half. Furthermore, the promoter knock-out elevated the migration ability of the edited cells. RNA se-quencing revealed many up- and downregulated genes involved in various cellular pathways, in-cluding epithelial to mesenchymal transition and mammary gland development pathways. Alto-gether, we are reporting here the existence of an additional/distal promoter with an enhancer effect on miR-29 generation and an inhibitory effect on cell migration.
 
Overall design RNA-seq transcriptome profiling of wild-type and C1orf132-edited MCF12A cells. 4 samples, 2 biological replicates for each condition.
 
Contributor(s) Malekzadeh Shafaroudi A, Sharifi-Zarchi A, Rahmani S, Nafissi N, Javad Mowla S, Lauria A, Oliviero S, M. Matin M
Citation(s) 34201896
Submission date Jun 07, 2021
Last update date Jul 10, 2021
Contact name Andrea Lauria
E-mail(s) andrea.lauria@unito.it
Organization name University of Turin
Department Life Sciences and Systems Biology
Lab Functional Genomics, Epigenomics - S. Oliviero
Street address Via Accademia Albertina, 13
City Turin
ZIP/Postal code 10123
Country Italy
 
Platforms (1)
GPL18573 Illumina NextSeq 500 (Homo sapiens)
Samples (4)
GSM5362434 WT_Rep1
GSM5362435 WT_Rep2
GSM5362436 KO_Rep1
Relations
BioProject PRJNA735745
SRA SRP323059

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
GSE176304_norm_counts.txt.gz 631.7 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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