Widespread employment of conserved C. elegans homeobox genes in neuronal identity specification.

Autor: Reilly MB; Department of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, New York, United States of America., Tekieli T; Department of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, New York, United States of America., Cros C; Department of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, New York, United States of America., Aguilar GR; Department of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, New York, United States of America., Lao J; Department of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, New York, United States of America., Toker IA; Department of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, New York, United States of America., Vidal B; Department of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, New York, United States of America., Leyva-Díaz E; Department of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, New York, United States of America., Bhattacharya A; Department of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, New York, United States of America., Cook SJ; Department of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, New York, United States of America., Smith JJ; Department of Neurobiology, University of Chicago, Chicago, Illinois, United States of America., Kovacevic I; Developmental Biology Program, Sloan Kettering Institute, New York, New York, United States of America., Gulez B; Department of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, New York, United States of America., Fernandez RW; Department of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, New York, United States of America., Bradford EF; Department of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, New York, United States of America., Ramadan YH; Department of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, New York, United States of America., Kratsios P; Department of Neurobiology, University of Chicago, Chicago, Illinois, United States of America., Bao Z; Developmental Biology Program, Sloan Kettering Institute, New York, New York, United States of America., Hobert O; Department of Biological Sciences, Columbia University, Howard Hughes Medical Institute, New York, New York, United States of America.
Jazyk: angličtina
Zdroj: PLoS genetics [PLoS Genet] 2022 Sep 30; Vol. 18 (9), pp. e1010372. Date of Electronic Publication: 2022 Sep 30 (Print Publication: 2022).
DOI: 10.1371/journal.pgen.1010372
Abstrakt: Homeobox genes are prominent regulators of neuronal identity, but the extent to which their function has been probed in animal nervous systems remains limited. In the nematode Caenorhabditis elegans, each individual neuron class is defined by the expression of unique combinations of homeobox genes, prompting the question of whether each neuron class indeed requires a homeobox gene for its proper identity specification. We present here progress in addressing this question by extending previous mutant analysis of homeobox gene family members and describing multiple examples of homeobox gene function in different parts of the C. elegans nervous system. To probe homeobox function, we make use of a number of reporter gene tools, including a novel multicolor reporter transgene, NeuroPAL, which permits simultaneous monitoring of the execution of multiple differentiation programs throughout the entire nervous system. Using these tools, we add to the previous characterization of homeobox gene function by identifying neuronal differentiation defects for 14 homeobox genes in 24 distinct neuron classes that are mostly unrelated by location, function and lineage history. 12 of these 24 neuron classes had no homeobox gene function ascribed to them before, while in the other 12 neuron classes, we extend the combinatorial code of transcription factors required for specifying terminal differentiation programs. Furthermore, we demonstrate that in a particular lineage, homeotic identity transformations occur upon loss of a homeobox gene and we show that these transformations are the result of changes in homeobox codes. Combining the present with past analyses, 113 of the 118 neuron classes of C. elegans are now known to require a homeobox gene for proper execution of terminal differentiation programs. Such broad deployment indicates that homeobox function in neuronal identity specification may be an ancestral feature of animal nervous systems.
Competing Interests: The authors have declared that no competing interests exist.
Databáze: MEDLINE
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