Spatial transcriptome profiling uncovers metabolic regulation of left-right patterning
Hisato YagiiD, Cheng Cui, Manush SaydmohammediD, George C. GabrieliD, Candice N. BakeriD, William A. DevineiD, Yijen L. WuiD, Jiuann-Huey Ivy LiniD, Marcus M. MalekiD, Abha Singh BaisiD, Stephen A. MurrayiD, Bruce J. AronowiD, Michael TsangiD, Dennis KostkaiD, Cecilia W. LoiD
Abstract
Left-right patterning disturbance can cause severe birth defects, but it remains least understood of the three body axes. We uncovered an unexpected role for metabolic regulation in left-right patterning. Analysis of the first spatial transcriptome profile of left-right patterning revealed global activation of glycolysis, accompanied by right-sided expression of Bmp7 and genes regulating insulin growth factor signaling. Cardiomyocyte differentiation was left-biased, which may underlie the specification of heart looping orientation. This is consistent with known Bmp7 stimulation of glycolysis and glycolysis suppression of cardiomyocyte differentiation. Liver/lung laterality may be specified via similar metabolic regulation of endoderm differentiation. Myo1d, found to be left-sided, was shown to regulate gut looping in mice, zebrafish, and human. Together these findings indicate metabolic regulation of left-right patterning. This could underlie high incidence of heterotaxy-related birth defects in maternal diabetes, and the association of PFKP, allosteric enzyme regulating glycolysis, with heterotaxy. This transcriptome dataset will be invaluable for interrogating birth defects involving laterality disturbance.
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