Explore the words cloud of the lincSAFARI project. It provides you a very rough idea of what is the project "lincSAFARI" about.
The following table provides information about the project.
WEIZMANN INSTITUTE OF SCIENCE
|Coordinator Country||Israel [IL]|
|Total cost||1˙500˙000 €|
|EC max contribution||1˙500˙000 € (100%)|
1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
|Duration (year-month-day)||from 2015-06-01 to 2020-05-31|
Take a look of project's partnership.
|1||WEIZMANN INSTITUTE OF SCIENCE||IL (REHOVOT)||coordinator||1˙500˙000.00|
It is now clear that many intergenic regions in eukaryotic genomes give rise to a range of processed and regulated transcripts that do not appear to code for functional proteins. A subset of these are long (>200 nt), capped and polyadenylated RNAs transcribed by RNA polymerase II and collectively called long intervening noncoding RNAs or lincRNAs. The recent estimates are that the human genome encodes >10,000 distinct lincRNAs, many of which show tissue-specific expression and are frequently dysregulated in human disease, including neurodegeneration.
Given the growing number of lincRNAs implicated in human disease or required for proper development, fundamental questions that need to be addressed are: Which lincRNAs are functional? How is functional information encoded in the lincRNA sequence? Is this information interpreted in the context of the mature or the nascent RNA? What are the identities and functional roles of specific sequence domains within lincRNA genes?
Our main hypothesis is that many lincRNA loci play key roles in gene regulation during cell differentiation, both via functionally important transcription events and post-transcriptionally, through the combined action of multiple short sequence domains. We will test this hypothesis using three complementary approaches – comparative genomics, detailed perturbations in mammalian cells followed by quantitative molecular phenotyping, and high-throughput screens for sequences able to carry out specific functions.
We propose an interdisciplinary approach combining computational, molecular and stem cell biology. Our methodology will be scalable, allowing us to tackle completely uncharacterized long RNAs and eventually zoom in and study their individual bases. Upon successful accomplishment of the program, we will delineate modes of action of numerous lincRNAs, report sequence patches that are functionally important and understand how specific bases and structures act in concert to drive lincRNA function.
|year||authors and title||journal||last update|
Aviv Rom, Liliya Melamed, Noa Gil, Micah Jonathan Goldrich, Rotem Kadir, Matan Golan, Inbal Biton, Rotem Ben-Tov Perry, Igor Ulitsky
Regulation of CHD2 expression by the Chaserr long noncoding RNA gene is essential for viability
published pages: , ISSN: 2041-1723, DOI: 10.1038/s41467-019-13075-8
|Nature Communications 10/1||2020-01-30|
Rotem Ben-Tov Perry, Hadas Hezroni, Micah Jonathan Goldrich, Igor Ulitsky
Regulation of Neuroregeneration by Long Noncoding RNAs
published pages: 553-567.e5, ISSN: 1097-2765, DOI: 10.1016/j.molcel.2018.09.021
|Molecular Cell 72/3||2020-01-30|
Noa Gil, Igor Ulitsky
Production of Spliced Long Noncoding RNAs Specifies Regions with Increased Enhancer Activity
published pages: 537-547.e3, ISSN: 2405-4712, DOI: 10.1016/j.cels.2018.10.009
|Cell Systems 7/5||2020-01-30|
Rotem Ben-Tov Perry, Igor Ulitsky
The functions of long noncoding RNAs in development and stem cells
published pages: 3882-3894, ISSN: 0950-1991, DOI: 10.1242/dev.140962
Hadas Hezroni, Rotem Ben-Tov Perry, Zohar Meir, Gali Housman, Yoav Lubelsky, Igor Ulitsky
A subset of conserved mammalian long non-coding RNAs are fossils of ancestral protein-coding genes
published pages: 162, ISSN: 1474-760X, DOI: 10.1186/s13059-017-1293-0
|Genome Biology 18/1||2019-06-05|
Ailone Tichon, Noa Gil, Yoav Lubelsky, Tal Havkin Solomon, Doron Lemze, Shalev Itzkovitz, Noam Stern-Ginossar, Igor Ulitsky
A conserved abundant cytoplasmic long noncoding RNA modulates repression by Pumilio proteins in human cells
published pages: 12209, ISSN: 2041-1723, DOI: 10.1038/ncomms12209
|Nature Communications 7||2019-06-05|
Ana Tamarkin-Ben-Harush, Jean-Jacques Vasseur, FranÃ§oise Debart, Igor Ulitsky, Rivka Dikstein
Cap-proximal nucleotides via differential eIF4E binding and alternative promoter usage mediate translational response to energy stress
published pages: , ISSN: 2050-084X, DOI: 10.7554/eLife.21907
Kathy Ushakov, Tal Koffler-Brill, Aviv Rom, Kobi Perl, Igor Ulitsky, Karen B. Avraham
Genome-wide identification and expression profiling of long non-coding RNAs in auditory and vestibular systems
published pages: , ISSN: 2045-2322, DOI: 10.1038/s41598-017-08320-3
|Scientific Reports 7/1||2019-06-05|
Evolution to the rescue: using comparative genomics to understand long non-coding RNAs
published pages: 601-614, ISSN: 1471-0056, DOI: 10.1038/nrg.2016.85
|Nature Reviews Genetics 17/10||2019-06-05|
Are you the coordinator (or a participant) of this project? Plaese send me more information about the "LINCSAFARI" project.
For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.
Send me an email (firstname.lastname@example.org) and I put them in your project's page as son as possible.
Thanks. And then put a link of this page into your project's website.
The information about "LINCSAFARI" are provided by the European Opendata Portal: CORDIS opendata.