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‘Glyco-deglyco’ processes during the synthesis of N-glycoproteins
For the past 15 years, it has appeared increasingly evident that the N-glycosylation process was accompanied by the release of oligomannoside type oligosaccharides. This material is constituted of oligosaccharide-phosphates and of neutral oligosaccharides possessing one GlcNAc (OS-Gn1) or two GlcNAc...
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Published in: | Biochimie 1998, Vol.80 (1), p.59-68 |
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description | For the past 15 years, it has appeared increasingly evident that the N-glycosylation process was accompanied by the release of oligomannoside type oligosaccharides. This material is constituted of oligosaccharide-phosphates and of neutral oligosaccharides possessing one GlcNAc (OS-Gn1) or two GlcNAc (OS-Gn2) at the reducing end. It has been demonstrated that oligosaccharide-phosphates originated from the cleavage by a specific pyrophosphatase, of non-glycosylated cytosolic faced oligosaccharide-PP-Dol and chiefly the Man
5GlcNAc
2-PP-Dol. The Man
5GlcNAc
2-P, as the main product, is recovered in the cytosolic compartment and is further degraded to Man
5GlcNAc
1 by as for yet not depicted enzymes. In contrast, OS-Gn2 produced from hydrolysis of oligosaccharide-PP-Dol (presumably as a transfer reaction onto water) when the amount of protein acceptor is limiting, are generated into the lumen of rough endoplasmic reticulum (ER). They are further submitted to processing α-glucosidases and rough ER mannosidase and are (mainly as Man
8GlcNAc
2) exported into the cytosolic compartment. This material is further degraded into a single compartment, the Man
5GlcNAc
1: Manα1-2Manα1-2Manα1–3 (Manα1–6)Manβ1-4GlcNAc by the sequential action of a cytosolic neutral chitobiase followed by cytosolic mannosidase. Furthermore, OS-Gn1 could have a dual origin: on the one hand, they originate from OS-Gn2 by the cytosolic degradation pathway indicated above: on the other hand, we will discuss a possible origin from the degradation or remodeling of newly synthesized glycoproteins. Considered first as a minor phenomenon, these observations have lead to the concept of intracellular oligomannoside trafficking, a process which results from more fundamental phenomena such as the control of the dolichol cycle, and the so-called quality-control of glycoprotein. In this review, we would like to describe the evolution of ideas on the origin, intracellular trafficking and putative roles of these oligomannosides released during the N-glycosylation process. We propose that these early stage ‘glyco-deglyco’ processes represent a way of control of N-glycosylation and of the fate of N-glycoproteins. |
doi_str_mv | 10.1016/S0300-9084(98)80057-6 |
format | article |
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5GlcNAc
2-PP-Dol. The Man
5GlcNAc
2-P, as the main product, is recovered in the cytosolic compartment and is further degraded to Man
5GlcNAc
1 by as for yet not depicted enzymes. In contrast, OS-Gn2 produced from hydrolysis of oligosaccharide-PP-Dol (presumably as a transfer reaction onto water) when the amount of protein acceptor is limiting, are generated into the lumen of rough endoplasmic reticulum (ER). They are further submitted to processing α-glucosidases and rough ER mannosidase and are (mainly as Man
8GlcNAc
2) exported into the cytosolic compartment. This material is further degraded into a single compartment, the Man
5GlcNAc
1: Manα1-2Manα1-2Manα1–3 (Manα1–6)Manβ1-4GlcNAc by the sequential action of a cytosolic neutral chitobiase followed by cytosolic mannosidase. Furthermore, OS-Gn1 could have a dual origin: on the one hand, they originate from OS-Gn2 by the cytosolic degradation pathway indicated above: on the other hand, we will discuss a possible origin from the degradation or remodeling of newly synthesized glycoproteins. Considered first as a minor phenomenon, these observations have lead to the concept of intracellular oligomannoside trafficking, a process which results from more fundamental phenomena such as the control of the dolichol cycle, and the so-called quality-control of glycoprotein. In this review, we would like to describe the evolution of ideas on the origin, intracellular trafficking and putative roles of these oligomannosides released during the N-glycosylation process. We propose that these early stage ‘glyco-deglyco’ processes represent a way of control of N-glycosylation and of the fate of N-glycoproteins.</description><identifier>ISSN: 0300-9084</identifier><identifier>EISSN: 1638-6183</identifier><identifier>DOI: 10.1016/S0300-9084(98)80057-6</identifier><identifier>PMID: 9587663</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Animals ; endoplasmic reticulum ; Glucosyltransferases - metabolism ; Glycoproteins - biosynthesis ; Glycosylation ; Humans ; lipid intermediates ; Models, Biological ; N-glycosylation ; oligomannoside trafficking ; Oligosaccharides - metabolism</subject><ispartof>Biochimie, 1998, Vol.80 (1), p.59-68</ispartof><rights>1998</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c360t-e50d50cab373f4715f37075829e3740e822fc2e79ab378c2978db622d3e6c1813</citedby><cites>FETCH-LOGICAL-c360t-e50d50cab373f4715f37075829e3740e822fc2e79ab378c2978db622d3e6c1813</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4023,27922,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9587663$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cacan, R.</creatorcontrib><creatorcontrib>Duvet, S.</creatorcontrib><creatorcontrib>Kmiécik, D.</creatorcontrib><creatorcontrib>Labiau, O.</creatorcontrib><creatorcontrib>Mir, A.M.</creatorcontrib><creatorcontrib>Verbert, A.</creatorcontrib><title>‘Glyco-deglyco’ processes during the synthesis of N-glycoproteins</title><title>Biochimie</title><addtitle>Biochimie</addtitle><description>For the past 15 years, it has appeared increasingly evident that the N-glycosylation process was accompanied by the release of oligomannoside type oligosaccharides. This material is constituted of oligosaccharide-phosphates and of neutral oligosaccharides possessing one GlcNAc (OS-Gn1) or two GlcNAc (OS-Gn2) at the reducing end. It has been demonstrated that oligosaccharide-phosphates originated from the cleavage by a specific pyrophosphatase, of non-glycosylated cytosolic faced oligosaccharide-PP-Dol and chiefly the Man
5GlcNAc
2-PP-Dol. The Man
5GlcNAc
2-P, as the main product, is recovered in the cytosolic compartment and is further degraded to Man
5GlcNAc
1 by as for yet not depicted enzymes. In contrast, OS-Gn2 produced from hydrolysis of oligosaccharide-PP-Dol (presumably as a transfer reaction onto water) when the amount of protein acceptor is limiting, are generated into the lumen of rough endoplasmic reticulum (ER). They are further submitted to processing α-glucosidases and rough ER mannosidase and are (mainly as Man
8GlcNAc
2) exported into the cytosolic compartment. This material is further degraded into a single compartment, the Man
5GlcNAc
1: Manα1-2Manα1-2Manα1–3 (Manα1–6)Manβ1-4GlcNAc by the sequential action of a cytosolic neutral chitobiase followed by cytosolic mannosidase. Furthermore, OS-Gn1 could have a dual origin: on the one hand, they originate from OS-Gn2 by the cytosolic degradation pathway indicated above: on the other hand, we will discuss a possible origin from the degradation or remodeling of newly synthesized glycoproteins. Considered first as a minor phenomenon, these observations have lead to the concept of intracellular oligomannoside trafficking, a process which results from more fundamental phenomena such as the control of the dolichol cycle, and the so-called quality-control of glycoprotein. In this review, we would like to describe the evolution of ideas on the origin, intracellular trafficking and putative roles of these oligomannosides released during the N-glycosylation process. We propose that these early stage ‘glyco-deglyco’ processes represent a way of control of N-glycosylation and of the fate of N-glycoproteins.</description><subject>Animals</subject><subject>endoplasmic reticulum</subject><subject>Glucosyltransferases - metabolism</subject><subject>Glycoproteins - biosynthesis</subject><subject>Glycosylation</subject><subject>Humans</subject><subject>lipid intermediates</subject><subject>Models, Biological</subject><subject>N-glycosylation</subject><subject>oligomannoside trafficking</subject><subject>Oligosaccharides - metabolism</subject><issn>0300-9084</issn><issn>1638-6183</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkM9OwkAQhzdGg4g-AklPRg_V2S7772QMQTQhelDPm7Kd4hpocbc14cZj6OvxJLZAuHr6Heab-WU-QvoUbihQcfsKDCDWoAZXWl0rAC5jcUS6VDAVC6rYMekekFNyFsInNBAkukM6mispBOuS0Wb9M56vbBlnOGtzs_6Nlr60GAKGKKu9K2ZR9YFRWBVNBBeiMo-e4y3cgBW6IpyTkzydB7zYZ4-8P4zeho_x5GX8NLyfxJYJqGLkkHGw6ZRJlg8k5TmTILlKNDI5AFRJktsEpW4JZRMtVTYVSZIxFJYqynrkcne3Kf6qMVRm4YLF-TwtsKyDkVpJzhRrQL4DrS9D8JibpXeL1K8MBdPqM1t9pnVjtDJbfUY0e_19QT1dYHbY2vtq5ne7OTZffjv0JliHhcXMebSVyUr3T8MfxFyArw</recordid><startdate>1998</startdate><enddate>1998</enddate><creator>Cacan, R.</creator><creator>Duvet, S.</creator><creator>Kmiécik, D.</creator><creator>Labiau, O.</creator><creator>Mir, A.M.</creator><creator>Verbert, A.</creator><general>Elsevier Masson SAS</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>1998</creationdate><title>‘Glyco-deglyco’ processes during the synthesis of N-glycoproteins</title><author>Cacan, R. ; Duvet, S. ; Kmiécik, D. ; Labiau, O. ; Mir, A.M. ; Verbert, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c360t-e50d50cab373f4715f37075829e3740e822fc2e79ab378c2978db622d3e6c1813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>endoplasmic reticulum</topic><topic>Glucosyltransferases - metabolism</topic><topic>Glycoproteins - biosynthesis</topic><topic>Glycosylation</topic><topic>Humans</topic><topic>lipid intermediates</topic><topic>Models, Biological</topic><topic>N-glycosylation</topic><topic>oligomannoside trafficking</topic><topic>Oligosaccharides - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cacan, R.</creatorcontrib><creatorcontrib>Duvet, S.</creatorcontrib><creatorcontrib>Kmiécik, D.</creatorcontrib><creatorcontrib>Labiau, O.</creatorcontrib><creatorcontrib>Mir, A.M.</creatorcontrib><creatorcontrib>Verbert, A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochimie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cacan, R.</au><au>Duvet, S.</au><au>Kmiécik, D.</au><au>Labiau, O.</au><au>Mir, A.M.</au><au>Verbert, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>‘Glyco-deglyco’ processes during the synthesis of N-glycoproteins</atitle><jtitle>Biochimie</jtitle><addtitle>Biochimie</addtitle><date>1998</date><risdate>1998</risdate><volume>80</volume><issue>1</issue><spage>59</spage><epage>68</epage><pages>59-68</pages><issn>0300-9084</issn><eissn>1638-6183</eissn><abstract>For the past 15 years, it has appeared increasingly evident that the N-glycosylation process was accompanied by the release of oligomannoside type oligosaccharides. This material is constituted of oligosaccharide-phosphates and of neutral oligosaccharides possessing one GlcNAc (OS-Gn1) or two GlcNAc (OS-Gn2) at the reducing end. It has been demonstrated that oligosaccharide-phosphates originated from the cleavage by a specific pyrophosphatase, of non-glycosylated cytosolic faced oligosaccharide-PP-Dol and chiefly the Man
5GlcNAc
2-PP-Dol. The Man
5GlcNAc
2-P, as the main product, is recovered in the cytosolic compartment and is further degraded to Man
5GlcNAc
1 by as for yet not depicted enzymes. In contrast, OS-Gn2 produced from hydrolysis of oligosaccharide-PP-Dol (presumably as a transfer reaction onto water) when the amount of protein acceptor is limiting, are generated into the lumen of rough endoplasmic reticulum (ER). They are further submitted to processing α-glucosidases and rough ER mannosidase and are (mainly as Man
8GlcNAc
2) exported into the cytosolic compartment. This material is further degraded into a single compartment, the Man
5GlcNAc
1: Manα1-2Manα1-2Manα1–3 (Manα1–6)Manβ1-4GlcNAc by the sequential action of a cytosolic neutral chitobiase followed by cytosolic mannosidase. Furthermore, OS-Gn1 could have a dual origin: on the one hand, they originate from OS-Gn2 by the cytosolic degradation pathway indicated above: on the other hand, we will discuss a possible origin from the degradation or remodeling of newly synthesized glycoproteins. Considered first as a minor phenomenon, these observations have lead to the concept of intracellular oligomannoside trafficking, a process which results from more fundamental phenomena such as the control of the dolichol cycle, and the so-called quality-control of glycoprotein. In this review, we would like to describe the evolution of ideas on the origin, intracellular trafficking and putative roles of these oligomannosides released during the N-glycosylation process. We propose that these early stage ‘glyco-deglyco’ processes represent a way of control of N-glycosylation and of the fate of N-glycoproteins.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>9587663</pmid><doi>10.1016/S0300-9084(98)80057-6</doi><tpages>10</tpages></addata></record> |
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subjects | Animals endoplasmic reticulum Glucosyltransferases - metabolism Glycoproteins - biosynthesis Glycosylation Humans lipid intermediates Models, Biological N-glycosylation oligomannoside trafficking Oligosaccharides - metabolism |
title | ‘Glyco-deglyco’ processes during the synthesis of N-glycoproteins |
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