Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2010-7-29
pubmed:abstractText
Non-coding RNAs (ncRNAs) are an essential class of molecular species that have been difficult to monitor on high throughput platforms due to frequent lack of polyadenylation. Using a polyadenylation-neutral amplification protocol and next-generation sequencing, we explore ncRNA expression in eleven human tissues. ncRNAs 7SL, U2, 7SK, and HBII-52 are expressed at levels far exceeding mRNAs. C/D and H/ACA box snoRNAs are associated with rRNA methylation and pseudouridylation, respectively: spleen expresses both, hypothalamus expresses mainly C/D box snoRNAs, and testes show enriched expression of both H/ACA box snoRNAs and RNA telomerase TERC. Within the snoRNA 14q cluster, 14q(I-6) is expressed at much higher levels than other cluster members. More reads align to mitochondrial than nuclear tRNAs. Many lincRNAs are actively transcribed, particularly those overlapping known ncRNAs. Within the Prader-Willi syndrome loci, the snoRNA HBII-85 (group I) cluster is highly expressed in hypothalamus, greater than in other tissues and greater than group II or III. Additionally, within the disease locus we find novel transcription across a 400,000 nt span in ovaries. This genome-wide polyA-neutral expression compendium demonstrates the richness of ncRNA expression, their high expression patterns, their function-specific expression patterns, and is publicly available.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-10192391, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-10902565, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-11106375, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-11701647, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-11733745, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-12045206, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-12457565, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-12520045, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-12970751, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-1423611, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-15479947, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-15770508, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-16381836, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-16617011, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-17015423, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-17194224, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-17270048, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-17854971, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-18006640, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-18283318, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-18500341, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-18516045, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-18996895, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-19217333, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-19379481, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-1953776, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-19571010, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-19668204, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-19917616, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-20124551, http://linkedlifedata.com/resource/pubmed/commentcorrection/20668672-2444875
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1932-6203
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
5
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
e11779
pubmed:meshHeading
pubmed:year
2010
pubmed:articleTitle
Digital genome-wide ncRNA expression, including SnoRNAs, across 11 human tissues using polyA-neutral amplification.
pubmed:affiliation
Institute for Translational Oncology and Immunology, Mainz, Germany. castle@uni-mainz.de
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't