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Zebrafish spinal cord oligodendrocyte formation requires boc function

Authors: Kearns, Christina A.; Walker, Macie; Ravanelli, Andrew M.; Scott, Kayt; Arzbecker, Madeline R.; Appel, Bruce

Online: https://academic.oup.com/genetics/article-abstract/218/4/iyab082/6289992

Issue: Genetics. 2021 Aug 9;218(4):iyab082.


The axis of the vertebrate neural tube is patterned, in part, by a ventral to dorsal gradient of Shh signaling. In the ventral spinal cord, Shh induces concentration-dependent expression of transcription factors, subdividing neural progenitors into distinct domains that subsequently produce distinct neuronal and glial subtypes. In particular, progenitors of the pMN domain express the bHLH transcription factor Olig2 and produce motor neurons followed by oligodendrocytes, the myelinating glial cell type of the central nervous system. In addition to its role in patterning ventral progenitors, Shh signaling must be maintained through development to specify pMN progenitors for oligodendrocyte fate. Using a forward genetic screen in zebrafish for mutations that disrupt development of oligodendrocytes, we identified a new mutant allele of boc , which encodes a type I transmembrane protein that functions as a coreceptor for Shh. Embryos homozygous for the boc co25 allele, which creates a missense mutation in a Fibronectin type III domain that binds Shh, have normally patterned spinal cords but fail to maintain pMN progenitors, resulting in a deficit of oligodendrocytes. Using a sensitive fluorescent detection method for in situ RNA hybridization, we found that spinal cord cells express boc in a graded fashion that is inverse to the gradient of Shh signaling activity and that boc function is necessary to maintain pMN progenitors by shaping the Shh signaling gradient.