Modulation of lineage-specific cell differentiation by long non-coding RNAs

Mammalian genomes comprise thousands of non-protein-coding genes. These can produce small non-coding RNAs (such as rRNAs and tRNAs), as well as long non-coding RNAs (lncRNAs), which are >200nt and resemble mRNAs in their biogenesis. Although the functions of the vast majority of lncRNAs remain unknown, many are tissue- and developmental stage-specific, suggesting roles in lineage-specific development. We generated deep transcriptome surveys from differentiating mouse red blood cells, and implemented a computational strategy for de novo lncRNA discovery to comprehensively catalog erythroid-expressed lncRNAs. We found >100 previously unannotated loci, many of which are erythroid-specific and are induced by key erythroid transcription factors during differentiation. We exploited these features to select 12 candidates for loss-of-function studies, and found that depleting 10 out of 12 impaired red cell maturation, inhibiting cell size reduction and subsequent enucleation. To study how lncRNAs regulate erythropoiesis, we focused on EC6, an unpolyadenylated lncRNA needed for silencing neighboring loci encoding NF-kB activators. De-repression of these genes upon EC6 knockdown leads to activation of NF-kB and other immune pathways that antagonize erythropoiesis, resulting in impaired proliferation and elevated apoptosis during differentiation. We showed that EC6 is retained in chromatin and binds the nuclear matrix factor hnRNP U, which may enable co-localization with its targets to mediate their repression. Extending our work to a different lineage, we reconstructed transcriptomes from distinct mouse adipose tissues and identified ~1500 lncRNAs. These included many brown fat-specific loci induced during differentiation which are targets of key adipogenic factors. Inhibiting one of them, lnc-BATE1, compromised brown adipocyte development, impairing activation of brown fat genes, mitochondrial biogenesis, and thermogenic function. We showed that lnc-BATE1 acts in trans and binds hnRNP U, which is also required for proper brown adipocyte maturation. This work demonstrates that lncRNAs modulate lineage-specific cell differentiation by promoting or suppressing competing gene expression programs controlling cell fate.

Department dc:contributor.department

Massachusetts Institute of Technology. Department of Biology.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2015

Author dc:creator

• Alvarez, Juan (Juan Rene Alvarez Dominguez)

Advisor dc:contributor.advisor

• Harvey F. Lodish and Alexander van Oudenaarden.

• Biology.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/97280

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/97280