Neurodevelopmental defects in human cortical organoids with N-acetylneuraminic acid synthase mutation.

Abstract

Biallelic genetic variants in N-acetylneuraminic acid synthase (NANS), a critical enzyme in endogenous sialic acid biosynthesis, are clinically associated with neurodevelopmental disorders. However, the mechanism underlying the neuropathological consequences has remained elusive. Here, we found that NANS mutation resulted in the absence of both sialic acid and protein polysialylation in the cortical organoids and notably reduced the proliferation and expansion of neural progenitors. NANS mutation dysregulated neural migration and differentiation, disturbed synapse formation, and weakened neuronal activity. Single-cell RNA sequencing revealed that NANS loss of function markedly altered transcriptional programs involved in neuronal differentiation and ribosomal biogenesis in various neuronal cell types. Similarly, Nans heterozygous mice exhibited impaired cortical neurogenesis and neurobehavioral deficits. Collectively, our findings reveal a crucial role of NANS-mediated endogenous sialic acid biosynthesis in regulating multiple features of human cortical development, thus linking NANS mutation with its clinically relevant neurodevelopmental disorders.

• Authors: Qian Bu, Yanping Dai, Huaqin Zhang, Min Li, Haxiaoyu Liu, Yan Huang, Ailing Zeng, Feng Qin, Linhong Jiang, Liang Wang, Yaxing Chen, Hongchun Li, Xiaojie Wang, Yue Zhao, Meng Qin, Ying Zhao, Ni Zhang, Weihong Kuang, Yinglan Zhao, Xiaobo Cen
• Journal: Science advances (Sci Adv) Vol. 9 Issue 47 Pg. eadf2772 (Nov 24 2023) ISSN: 2375-2548 [Electronic] United States
• PMID: 38000033 (Publication Type: Journal Article)

Chemical References

• N-Acetylneuraminic Acid
• N-acetylneuraminate synthase
• Oxo-Acid-Lyases

Topics

• Humans
• Mice
• Animals
• N-Acetylneuraminic Acid (metabolism)
• Oxo-Acid-Lyases (genetics)
• Organoids (metabolism)
• Mutation
• Neurogenesis (genetics)