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Publication : A KO mouse model for the lncRNA Lhx1os produces motor neuron alterations and locomotor impairment.

First Author  Pellegrini F Year  2023
Journal  iScience Volume  26
Issue  1 Pages  105891
PubMed ID  36647387 Mgi Jnum  J:332662
Mgi Id  MGI:7428166 Doi  10.1016/j.isci.2022.105891
Citation  Pellegrini F, et al. (2023) A KO mouse model for the lncRNA Lhx1os produces motor neuron alterations and locomotor impairment. iScience 26(1):105891
abstractText  Here, we describe a conserved motor neuron-specific long non-coding RNA, Lhx1os, whose knockout in mice produces motor impairment and postnatal reduction of mature motor neurons (MNs). The ER stress-response pathway result specifically altered with the downregulation of factors involved in the unfolded protein response (UPR). Lhx1os was found to bind the ER-associated PDIA3 disulfide isomerase and to affect the expression of the same set of genes controlled by this protein, indicating that the two factors act in conjunction to modulate the UPR. Altogether, the observed phenotype and function of Lhx1os indicate its important role in the control of MN homeostasis and function.
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