NXPE1 alters the sialoglycome by acetylating sialic acids in the human colon

Mild periodic acid Schiff staining (mPAS) of human colonic tissue has been used to answer a variety of fundamental questions in germline and somatic genetics. mPAS stains sialic acids except when these glycans are modified by O-acetylation, but a full accounting of the genes contributing to sialoglycan acetylation is incomplete. Using haplotypes derived from whole genome sequencing, we identify a region on chromosome 11 that is associated with inherited differences in mPAS staining. Of the genes in this region, only haplotypes containing NXPE1 correlate perfectly with mPAS staining in the original cohort used for whole genome sequencing, as well as in a validation cohort. Transcriptomic analysis indicates that linked haplotypes are associated with altered expression of NXPE1 suggesting a possible genetic mechanism. Genetic manipulation of a common single nucleotide polymorphism observed in the haplotype region and located in NXPE1's promoter alters expression and causes changes to modified sialic acid levels supporting this mechanism. Finally, high-performance liquid chromatography (HPLC) confirms that enzymatically active NXPE1 is capable of transferring an acetyl group from acetyl coenzyme A to sialic acid in vitro. These findings suggest that NXPE1 is the long-sought gene responsible for differences in colon mPAS staining and may be the prototype of a new family of sialic acid O-acetylation-modifying genes.

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Publication Details

Journal
Nature Communications
Published
2025-05-27
DOI
https://doi.org/10.1038/s41467-025-59671-9
Citations
2
Primary Topic
Glycosylation and Glycoproteins Research
Type
article
Field-Weighted Citation Impact
1.61

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article

NXPE1 alters the sialoglycome by acetylating sialic acids in the human colon

Phillip Buckhaults, Surojit Sur, Nickolas Papadopoulos, Sana Khalili et al.
2 citations
Nature Communications
Glycosylation and Glycoproteins Research
1.61
article

NXPE1 alters the sialoglycome by acetylating sialic acids in the human colon

Phillip Buckhaults, Surojit Sur, Nickolas Papadopoulos, Sana Khalili, Maria Popoli, Kathleen L. Gabrielson, Kenneth W. Kinzler, Chetan Bettegowda, Bert Vogelstein, Ashley L. Cook, Nicolas Wyhs, Laura Dobbyn, Shibin Zhou, Bum Seok Lee
article en
2 citations

Abstract

Mild periodic acid Schiff staining (mPAS) of human colonic tissue has been used to answer a variety of fundamental questions in germline and somatic genetics. mPAS stains sialic acids except when these glycans are modified by O-acetylation, but a full accounting of the genes contributing to sialoglycan acetylation is incomplete. Using haplotypes derived from whole genome sequencing, we identify a region on chromosome 11 that is associated with inherited differences in mPAS staining. Of the genes in this region, only haplotypes containing NXPE1 correlate perfectly with mPAS staining in the original cohort used for whole genome sequencing, as well as in a validation cohort. Transcriptomic analysis indicates that linked haplotypes are associated with altered expression of NXPE1 suggesting a possible genetic mechanism. Genetic manipulation of a common single nucleotide polymorphism observed in the haplotype region and located in NXPE1's promoter alters expression and causes changes to modified sialic acid levels supporting this mechanism. Finally, high-performance liquid chromatography (HPLC) confirms that enzymatically active NXPE1 is capable of transferring an acetyl group from acetyl coenzyme A to sialic acid in vitro. These findings suggest that NXPE1 is the long-sought gene responsible for differences in colon mPAS staining and may be the prototype of a new family of sialic acid O-acetylation-modifying genes.

Nature CommunicationsVol. 16(1)
Howard Hughes Medical Institute (US), Johns Hopkins University (US), University of South Carolina (US), Johns Hopkins Medicine (US), Cancer Research Center (US), Cancer Genetics (United States) (US)
Howard Hughes Medical Institute, Commonwealth Fund, Lustgarten Foundation, Virginia and D.K. Ludwig Fund for Cancer Research, Johns Hopkins University, Ludwig Institute for Cancer Research, National Institutes of Health, Sidney Kimmel Comprehensive Cancer Center, National Heart, Lung, and Blood Institute, National Institute of Mental Health, National Institute on Drug Abuse, National Human Genome Research Institute, NIH Office of the Director, National Cancer Institute, National Institute of Neurological Disorders and Stroke, Common Fund
Openalex Percentile: Top 17%
Glycosylation and Glycoproteins Research
1.61
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