Pnky lncRNA secondary structure maps identify functional regions that control neurogenesis in neural stem cells.
Overview
- Department of Neurological Surgery, University of California, San Francisco, San Francisco, CA 94143, USA
- Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, CA 94143, USA
- San Francisco Veterans Affairs Medical Center, San Francisco, CA 94121, USA
- These authors contributed equally
- Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06511, USA
- Department of Chemistry, Yale University, New Haven, CT 06511, USA
- Cancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK
- Department of Molecular and Cell Biology Undergraduate Program, University of California, Berkeley, Berkeley, CA 94720, USA
- Division of Genetics and Genomics, Harvard Medical School, Boston Children’s Hospital, Boston, MA 02115, USA
- Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT 06511, USA
- Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA
- Lead contact
Abstract
Long noncoding RNA (lncRNA) Pnky is a trans-acting regulator of neural stem cell (NSC) differentiation, but the molecular mechanisms by which Pnky regulates neurogenesis are unknown. A fundamental step toward mechanistic understanding is to determine whether lncRNA structure underlies biological function. Using chemical probing and high-throughput analysis, we determined the secondary structure of Pnky folded in vitro and in cellulo. In vitro-transcribed Pnky RNA adopts a compact, highly structured conformation with evidence of tertiary interactions. In cellulo, Pnky secondary structure is similar to the in vitro conformation. We used locked nucleic acid (LNA) oligonucleotides to interrogate the entire Pnky transcript for function in NSCs and identified regions that when targeted increase neurogenesis—phenocopyin
Reproduced under the paper's license (CC BY), from the paper cited above.
Code
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Data
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Data and code availability
SHAPE-MaP and terbium-seq data have been deposited in the NCBI SRA database under the identifier BioProject ID: PRJNA1263515.
This paper does not report original code.
Any additional information required to reanalyze the data reported in this paper is available from the lead contact upon request.
Reproduced under the paper's license (CC BY), from the paper cited above.
Versions
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Version 2, 28 September 2026
- Publisher: n/a → Cell Press
Version 1, 28 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 8 authors, 10 keywords, 8 MeSH terms, 9 funders, 77 references, 1 RRID.
Cite
This paper
Saha, P., Patel, S., Tsao, L. H., Tavares, R. C., Choi, H., Andersen, R. E., Pyle, A. M., & Lim, D. A. (2026). Pnky lncRNA secondary structure maps identify functional regions that control neurogenesis in neural stem cells. Cell reports, 45(6), 117451. https://
BibTeX
@article{saha2026pnky,
author = {Saha, Parna and Patel, Shivali and Tsao, Lucille H. and Tavares, Rafael CA. and Choi, Hyeonseok and Andersen, Rebecca E. and Pyle, Anna Marie and Lim, Daniel A.},
title = {{Pnky lncRNA secondary structure maps identify functional regions that control neurogenesis in neural stem cells}},
journal = {Cell reports},
year = {2026},
month = may,
volume = {45},
number = {6},
pages = {117451},
publisher = {Cell Press},
issn = {2211-1247},
doi = {10.1016/
url = {https://
pmid = {42213787},
pmcid = {PMC13446462}
}
RIS
TY - JOUR
AU - Saha, Parna
AU - Patel, Shivali
AU - Tsao, Lucille H.
AU - Tavares, Rafael CA.
AU - Choi, Hyeonseok
AU - Andersen, Rebecca E.
AU - Pyle, Anna Marie
AU - Lim, Daniel A.
TI - Pnky lncRNA secondary structure maps identify functional regions that control neurogenesis in neural stem cells
T2 - Cell reports
J2 - Cell Rep
PY - 2026
DA - 2026/
VL - 45
IS - 6
SP - 117451
SN - 2211-1247
PB - Cell Press
DO - 10.1016/
UR - https://
LA - en
ER -
CSL-JSON
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