标题:"Coding" and "Decoding": hypothesis for the regulatory mechanism involved in heparan sulfate biosynthesis
作者:Zhang, Xu; Wang, Fengshan; Sheng, Juzheng
作者机构:[Zhang, Xu; Wang, Fengshan; Sheng, Juzheng] Shandong Univ, Sch Pharmaceut Sci, Inst Biochem & Biotechnol Drugs, Key Lab Chem Biol Nat Prod,Minist Educ 更多
通讯作者:Wang, Fengshan
通讯作者地址:[Wang, FS; Sheng, JZ]Shandong Univ, Sch Pharmaceut Sci, Inst Biochem & Biotechnol Drugs, Key Lab Chem Biol Nat Prod,Minist Educ, Jinan 250012, Peoples 更多
来源:CARBOHYDRATE RESEARCH
出版年:2016
卷:428
页码:1-7
DOI:10.1016/j.carres.2016.04.002
关键词:Heparan sulfate; N-deacetylase/N-sulfotransferase; C5-epimerase;; O-sulfotransferase; Biosynthesis mechanism
摘要:Heparan sulfate (HS) is widely distributed in mammalian tissues in the form of HS proteoglycans, which play essential roles in various physiological and pathological processes. In contrast to the template-guided processes involved in the synthesis of DNA and proteins, HS biosynthesis is not believed to involve a template. However, it appears that the final structure of HS chains was strictly regulated. Herein, we report research based hypothesis that two major steps, namely "coding" and "decoding" steps, are involved in the biosynthesis of HS, which strictly regulate its chemical structure and biological activity. The "coding" process in this context is based on the distribution of sulfate moieties on the amino groups of the glucosamine residues in the HS chains. The sulfation of these amine groups is catalyzed by N-deacetylase/N-sulfotransferase, which has four isozymes. The composition and distribution of sulfate groups and iduronic acid residues on the glycan chains of HS are determined by several other modification enzymes, which can recognize these coding sequences (i.e., the "decoding" process). The degree and pattern of the sulfation and epimerization in the HS chains determines the extent of their interactions with several different protein factors, which further influences their biological activity. (C) 2016 Elsevier Ltd. All rights reserved.
收录类别:EI;SCOPUS;SCIE
WOS核心被引频次:5
Scopus被引频次:6
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84963535702&doi=10.1016%2fj.carres.2016.04.002&partnerID=40&md5=937fb621d0bfd84e3fdcf951323c1a72
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