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溃疡性结肠炎相关基因NXPE1催化结肠粘蛋白的聚糖修饰。

The Ulcerative Colitis-Associated Gene NXPE1 Catalyzes Glycan Modifications on Colonic Mucin.

作者信息

Humeidi Ranad, Oshiro-Rapley Noriko, Gu Xiebin, An Joon Soo, Ananthakrishnan Ashwin N, Creasey Elizabeth A, Daly Mark J, Schreiber Stuart L, Graham Daniel B, Seyedsayamdost Mohammad R, Xavier Ramnik J

机构信息

Program for Chemistry & Chemical Biology, Harvard Medical School, Boston, Massachusetts 02115, United States.

Broad Institute of MIT and Harvard, Cambridge, Massachusetts 02141, United States.

出版信息

J Am Chem Soc. 2025 Mar 26;147(12):10618-10628. doi: 10.1021/jacs.5c00769. Epub 2025 Mar 11.

Abstract

Colonic mucus forms a first line of defense against bacterial invasion while providing nutrition to support coinhabiting microbes in the gut. Mucus is composed of polymeric networks of mucin proteins, which are heavily modified post-translationally. The full compendium of enzymes responsible for these modifications and their roles in health and disease remain incompletely understood. Herein, we determine the biochemical function of , a gene implicated in ulcerative colitis (UC), and demonstrate that it encodes an acetyltransferase that modifies mucin glycans. Specifically, NXPE1 utilizes acetyl-CoA to regioselectively modify the mucus sialic acid, 5--acetylneuraminic acid (Neu5Ac), at the 9-OH group to generate 9--acetylated Neu5Ac (Neu5,9Ac). We further demonstrate that colonic organoids derived from donors harboring the missense variant NXPE1 G353R, which is protective against UC, exhibit severely impaired acetylation of Neu5Ac on mucins. Together, our findings support a model in which NXPE1 masks the alcohols of mucus sialoglycans via acetylation, which is important for modulating mucus barrier properties that limit interactions with commensal microbes.

摘要

结肠黏液形成了抵御细菌入侵的第一道防线,同时为肠道中共存的微生物提供营养支持。黏液由黏蛋白的聚合物网络组成,这些黏蛋白在翻译后会发生大量修饰。负责这些修饰的酶的完整清单及其在健康和疾病中的作用仍未完全了解。在此,我们确定了与溃疡性结肠炎(UC)相关的基因 的生化功能,并证明它编码一种修饰黏蛋白聚糖的乙酰转移酶。具体而言,NXPE1利用乙酰辅酶A对黏液唾液酸、5-乙酰神经氨酸(Neu5Ac)的9-OH基团进行区域选择性修饰,生成9-乙酰化Neu5Ac(Neu5,9Ac)。我们进一步证明,来自携带错义变体NXPE1 G353R(对UC有保护作用)的供体的结肠类器官,其黏蛋白上Neu5Ac的乙酰化严重受损。总之,我们的研究结果支持了一种模型,即NXPE1通过乙酰化掩盖黏液唾液酸聚糖的醇类,这对于调节限制与共生微生物相互作用的黏液屏障特性很重要。

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Mucus sialylation determines intestinal host-commensal homeostasis.黏蛋白唾液酸化决定肠道共生稳态。
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