<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>27(6)</volume><submitter>Linsley PS</submitter><pubmed_abstract>microRNAs (miRNAs) are abundant, approximately 21-nucleotide, noncoding regulatory RNAs. Each miRNA may regulate hundreds of mRNA targets, but the identities of these targets and the processes they regulate are poorly understood. Here we have explored the use of microarray profiling and functional screening to identify targets and biological processes triggered by the transfection of human cells with miRNAs. We demonstrate that a family of miRNAs sharing sequence identity with miRNA-16 (miR-16) negatively regulates cellular growth and cell cycle progression. miR-16-down-regulated transcripts were enriched with genes whose silencing by small interfering RNAs causes an accumulation of cells in G(0)/G(1). Simultaneous silencing of these genes was more effective at blocking cell cycle progress</pubmed_abstract><journal>Molecular and cellular biology</journal><pagination>2240-52</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC1820501</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Transcripts targeted by the microRNA-16 family cooperatively regulate cell cycle progression.</pubmed_title><pmcid>PMC1820501</pmcid><pubmed_authors>Johnson JM</pubmed_authors><pubmed_authors>Raymond CK</pubmed_authors><pubmed_authors>Bartz SR</pubmed_authors><pubmed_authors>Cleary M</pubmed_authors><pubmed_authors>Carleton M</pubmed_authors><pubmed_authors>Burchard J</pubmed_authors><pubmed_authors>Cummins JM</pubmed_authors><pubmed_authors>Kibukawa M</pubmed_authors><pubmed_authors>Linsley PS</pubmed_authors><pubmed_authors>Chau N</pubmed_authors><pubmed_authors>Jackson AL</pubmed_authors><pubmed_authors>Lim L</pubmed_authors><pubmed_authors>Schelter J</pubmed_authors><pubmed_authors>Martin MM</pubmed_authors><pubmed_authors>Dai H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcripts targeted by the microRNA-16 family cooperatively regulate cell cycle progression.</name><description>microRNAs (miRNAs) are abundant, approximately 21-nucleotide, noncoding regulatory RNAs. Each miRNA may regulate hundreds of mRNA targets, but the identities of these targets and the processes they regulate are poorly understood. Here we have explored the use of microarray profiling and functional screening to identify targets and biological processes triggered by the transfection of human cells with miRNAs. We demonstrate that a family of miRNAs sharing sequence identity with miRNA-16 (miR-16) negatively regulates cellular growth and cell cycle progression. miR-16-down-regulated transcripts were enriched with genes whose silencing by small interfering RNAs causes an accumulation of cells in G(0)/G(1). Simultaneous silencing of these genes was more effective at blocking cell cycle progress</description><dates><release>2007-01-01T00:00:00Z</release><publication>2007 Mar</publication><modification>2025-04-05T10:04:26.358Z</modification><creation>2019-03-27T02:03:32Z</creation></dates><accession>S-EPMC1820501</accession><cross_references><pubmed>17242205</pubmed><doi>10.1128/MCB.02005-06</doi><doi>10.1128/mcb.02005-06</doi></cross_references></HashMap>