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Systematic Analysis of the Lysine Crotonylome and Multiple Posttranslational Modification Analysis (Acetylation, Succinylation, and Crotonylation) in Candida albicans
is an opportunistic pathogen that causes lethal fungal infections in immunocompromised patients. Lysine crotonylation is a newly discovered PTM (posttranslational modification) epigenetic type that may play a critical role in regulating gene expression. In this study, we used an antibody-enrichment...
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description | is an opportunistic pathogen that causes lethal fungal infections in immunocompromised patients. Lysine crotonylation is a newly discovered PTM (posttranslational modification) epigenetic type that may play a critical role in regulating gene expression. In this study, we used an antibody-enrichment approach along with LC-MS/MS to carry out a quantitative crotonylome analysis in
We found a total of 5,242 crotonylation sites and 1,584 crotonylated proteins among 9,038 proteins in this organism. Of these crotonylated proteins, a few unique crotonylated motifs are noted such as D and E in positions +1, +2, or +3 or K and R in positions +5 or +6, while A, E, F, G, P, W, and Y are in the -1 position or A, K, and R are found in positions -5, -6, -7, or -8. Functional analysis has shown that a majority of the crotonylated proteins are related to biosynthetic events and carbon metabolism. When combined with previously collected data on acetylation and succinylation, PPI (protein-protein interaction network) analysis reveals that proteins with functions in ribosomal biogenesis, oxidative phosphorylation, nucleus activity, and proteasome formation are heavily modified by these three PTM types. To the best of our knowledge, this is the first crotonylome study carried out in
and is an important step to a better understanding of the biological and pathogenic impact of PTM in
is a kind of pathogen of fungal infections that is found worldwide. Lysine crotonylation of proteins as a recently discovered PTM (posttranslational modification) may have a critical role in regulating cells. We first carried out large-scale analysis of crotonylated proteome and multiple PTM analysis (acetylation, succinylation, and crotonylation), then drew a diagram to show multiple PTM sites on histones in
of our study. This study about crotonylome in human pathogenic fungi is a milestone that first and deeply investigates the functional analysis of crotonylated proteins in
, which marks an important start for further research. |
doi_str_mv | 10.1128/mSystems.01316-20 |
format | article |
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We found a total of 5,242 crotonylation sites and 1,584 crotonylated proteins among 9,038 proteins in this organism. Of these crotonylated proteins, a few unique crotonylated motifs are noted such as D and E in positions +1, +2, or +3 or K and R in positions +5 or +6, while A, E, F, G, P, W, and Y are in the -1 position or A, K, and R are found in positions -5, -6, -7, or -8. Functional analysis has shown that a majority of the crotonylated proteins are related to biosynthetic events and carbon metabolism. When combined with previously collected data on acetylation and succinylation, PPI (protein-protein interaction network) analysis reveals that proteins with functions in ribosomal biogenesis, oxidative phosphorylation, nucleus activity, and proteasome formation are heavily modified by these three PTM types. To the best of our knowledge, this is the first crotonylome study carried out in
and is an important step to a better understanding of the biological and pathogenic impact of PTM in
is a kind of pathogen of fungal infections that is found worldwide. Lysine crotonylation of proteins as a recently discovered PTM (posttranslational modification) may have a critical role in regulating cells. We first carried out large-scale analysis of crotonylated proteome and multiple PTM analysis (acetylation, succinylation, and crotonylation), then drew a diagram to show multiple PTM sites on histones in
of our study. This study about crotonylome in human pathogenic fungi is a milestone that first and deeply investigates the functional analysis of crotonylated proteins in
, which marks an important start for further research.</description><identifier>ISSN: 2379-5077</identifier><identifier>EISSN: 2379-5077</identifier><identifier>DOI: 10.1128/mSystems.01316-20</identifier><identifier>PMID: 33500332</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Candida albicans ; crotonylome ; histone ; lysine crotonylation motif ; Molecular Biology and Physiology ; PPI analysis ; Research Article</subject><ispartof>mSystems, 2021-01, Vol.6 (1)</ispartof><rights>Copyright © 2021 Zhou et al.</rights><rights>Copyright © 2021 Zhou et al. 2021 Zhou et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a504t-b0b5605fb20d549534464bd204eeac9c4d724d158e15ac524fdea091d3e6ca513</citedby><cites>FETCH-LOGICAL-a504t-b0b5605fb20d549534464bd204eeac9c4d724d158e15ac524fdea091d3e6ca513</cites><orcidid>0000-0002-5148-2922</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.asm.org/doi/pdf/10.1128/mSystems.01316-20$$EPDF$$P50$$Gasm2$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://journals.asm.org/doi/full/10.1128/mSystems.01316-20$$EHTML$$P50$$Gasm2$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,27924,27925,37013,52751,52752,52753,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33500332$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Fenyo, David</contributor><creatorcontrib>Zhou, Xiaowei</creatorcontrib><creatorcontrib>Song, Nana</creatorcontrib><creatorcontrib>Li, Dongmei</creatorcontrib><creatorcontrib>Li, Xiaofang</creatorcontrib><creatorcontrib>Liu, Weida</creatorcontrib><title>Systematic Analysis of the Lysine Crotonylome and Multiple Posttranslational Modification Analysis (Acetylation, Succinylation, and Crotonylation) in Candida albicans</title><title>mSystems</title><addtitle>mSystems</addtitle><addtitle>mSystems</addtitle><description>is an opportunistic pathogen that causes lethal fungal infections in immunocompromised patients. Lysine crotonylation is a newly discovered PTM (posttranslational modification) epigenetic type that may play a critical role in regulating gene expression. In this study, we used an antibody-enrichment approach along with LC-MS/MS to carry out a quantitative crotonylome analysis in
We found a total of 5,242 crotonylation sites and 1,584 crotonylated proteins among 9,038 proteins in this organism. Of these crotonylated proteins, a few unique crotonylated motifs are noted such as D and E in positions +1, +2, or +3 or K and R in positions +5 or +6, while A, E, F, G, P, W, and Y are in the -1 position or A, K, and R are found in positions -5, -6, -7, or -8. Functional analysis has shown that a majority of the crotonylated proteins are related to biosynthetic events and carbon metabolism. When combined with previously collected data on acetylation and succinylation, PPI (protein-protein interaction network) analysis reveals that proteins with functions in ribosomal biogenesis, oxidative phosphorylation, nucleus activity, and proteasome formation are heavily modified by these three PTM types. To the best of our knowledge, this is the first crotonylome study carried out in
and is an important step to a better understanding of the biological and pathogenic impact of PTM in
is a kind of pathogen of fungal infections that is found worldwide. Lysine crotonylation of proteins as a recently discovered PTM (posttranslational modification) may have a critical role in regulating cells. We first carried out large-scale analysis of crotonylated proteome and multiple PTM analysis (acetylation, succinylation, and crotonylation), then drew a diagram to show multiple PTM sites on histones in
of our study. This study about crotonylome in human pathogenic fungi is a milestone that first and deeply investigates the functional analysis of crotonylated proteins in
, which marks an important start for further research.</description><subject>Candida albicans</subject><subject>crotonylome</subject><subject>histone</subject><subject>lysine crotonylation motif</subject><subject>Molecular Biology and Physiology</subject><subject>PPI analysis</subject><subject>Research Article</subject><issn>2379-5077</issn><issn>2379-5077</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kttuEzEQhlcIRKvSB-AG-bJIJPi4hxukKOJQKRVIhWtr1va2jrx2WHsr7QvxnDjZJrQ3XNkznv_75ZkpircELwmh9cf-dorJ9HGJCSPlguIXxTllVbMQuKpePrmfFZcxbjHGpGQVoc3r4owxgTFj9Lz4M1MgWYVWHtwUbUShQ-neoE0OvEHrIaTgJxd6g8BrdDO6ZHfOoB8hpjSAjy7LQxajm6BtZ9Uh_Ie7WimTprnoA7odlbL-FO6JR4dD6j2yHq1z2mpA4NqM8_FN8aoDF83l43lR_Pry-ef622Lz_ev1erVZgMA8LVrcihKLrqVYC94IxnnJW00xNwZUo7iuKNdE1IYIUILyThvADdHMlAoEYRfF9czVAbZyN9gehkkGsPKQCMOdhCH3yhlJKqJAN12ldHahtO0E57VumroDEF2ZWZ9m1m5se6OV8blZ7hn0-Yu39_IuPMiq5pSVe8DVI2AIv0cTk-xtVMY58CaMUVJe55HWvN6XkrlUDSHGwXQnG4Llfl3kcV3kYV0kxVmznDUQeyq3YRzywOJ_Be-efuhkcdwm9hdhL9HS</recordid><startdate>20210126</startdate><enddate>20210126</enddate><creator>Zhou, Xiaowei</creator><creator>Song, Nana</creator><creator>Li, Dongmei</creator><creator>Li, Xiaofang</creator><creator>Liu, Weida</creator><general>American Society for Microbiology</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-5148-2922</orcidid></search><sort><creationdate>20210126</creationdate><title>Systematic Analysis of the Lysine Crotonylome and Multiple Posttranslational Modification Analysis (Acetylation, Succinylation, and Crotonylation) in Candida albicans</title><author>Zhou, Xiaowei ; Song, Nana ; Li, Dongmei ; Li, Xiaofang ; Liu, Weida</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a504t-b0b5605fb20d549534464bd204eeac9c4d724d158e15ac524fdea091d3e6ca513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Candida albicans</topic><topic>crotonylome</topic><topic>histone</topic><topic>lysine crotonylation motif</topic><topic>Molecular Biology and Physiology</topic><topic>PPI analysis</topic><topic>Research Article</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Xiaowei</creatorcontrib><creatorcontrib>Song, Nana</creatorcontrib><creatorcontrib>Li, Dongmei</creatorcontrib><creatorcontrib>Li, Xiaofang</creatorcontrib><creatorcontrib>Liu, Weida</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>mSystems</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Xiaowei</au><au>Song, Nana</au><au>Li, Dongmei</au><au>Li, Xiaofang</au><au>Liu, Weida</au><au>Fenyo, David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Systematic Analysis of the Lysine Crotonylome and Multiple Posttranslational Modification Analysis (Acetylation, Succinylation, and Crotonylation) in Candida albicans</atitle><jtitle>mSystems</jtitle><stitle>mSystems</stitle><addtitle>mSystems</addtitle><date>2021-01-26</date><risdate>2021</risdate><volume>6</volume><issue>1</issue><issn>2379-5077</issn><eissn>2379-5077</eissn><abstract>is an opportunistic pathogen that causes lethal fungal infections in immunocompromised patients. Lysine crotonylation is a newly discovered PTM (posttranslational modification) epigenetic type that may play a critical role in regulating gene expression. In this study, we used an antibody-enrichment approach along with LC-MS/MS to carry out a quantitative crotonylome analysis in
We found a total of 5,242 crotonylation sites and 1,584 crotonylated proteins among 9,038 proteins in this organism. Of these crotonylated proteins, a few unique crotonylated motifs are noted such as D and E in positions +1, +2, or +3 or K and R in positions +5 or +6, while A, E, F, G, P, W, and Y are in the -1 position or A, K, and R are found in positions -5, -6, -7, or -8. Functional analysis has shown that a majority of the crotonylated proteins are related to biosynthetic events and carbon metabolism. When combined with previously collected data on acetylation and succinylation, PPI (protein-protein interaction network) analysis reveals that proteins with functions in ribosomal biogenesis, oxidative phosphorylation, nucleus activity, and proteasome formation are heavily modified by these three PTM types. To the best of our knowledge, this is the first crotonylome study carried out in
and is an important step to a better understanding of the biological and pathogenic impact of PTM in
is a kind of pathogen of fungal infections that is found worldwide. Lysine crotonylation of proteins as a recently discovered PTM (posttranslational modification) may have a critical role in regulating cells. We first carried out large-scale analysis of crotonylated proteome and multiple PTM analysis (acetylation, succinylation, and crotonylation), then drew a diagram to show multiple PTM sites on histones in
of our study. This study about crotonylome in human pathogenic fungi is a milestone that first and deeply investigates the functional analysis of crotonylated proteins in
, which marks an important start for further research.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>33500332</pmid><doi>10.1128/mSystems.01316-20</doi><tpages>19</tpages><orcidid>https://orcid.org/0000-0002-5148-2922</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Candida albicans crotonylome histone lysine crotonylation motif Molecular Biology and Physiology PPI analysis Research Article |
title | Systematic Analysis of the Lysine Crotonylome and Multiple Posttranslational Modification Analysis (Acetylation, Succinylation, and Crotonylation) in Candida albicans |
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