Loading…
Chromatin-remodeling factor CHR721 with non-canonical PIP-box interacts with OsPCNA in Rice
Proliferating cell nuclear antigen (PCNA) is one of the key factors for the DNA replication process and DNA damage repair. Most proteins interacting with PCNA have a common binding motif: PCNA interacting protein box (PIP box). However, some proteins with non-canonical PIP-box have also been reporte...
Saved in:
Published in: | BMC plant biology 2022-04, Vol.22 (1), p.164-164, Article 164 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c426t-fcfcc469297bec5e1f9301a054741c5c1e947275d5402f743dbb9071e814d2e03 |
---|---|
cites | cdi_FETCH-LOGICAL-c426t-fcfcc469297bec5e1f9301a054741c5c1e947275d5402f743dbb9071e814d2e03 |
container_end_page | 164 |
container_issue | 1 |
container_start_page | 164 |
container_title | BMC plant biology |
container_volume | 22 |
creator | Zhang, Yushun Chen, Qiong Zhu, Guanlin Zhang, Dechun Liang, Weihong |
description | Proliferating cell nuclear antigen (PCNA) is one of the key factors for the DNA replication process and DNA damage repair. Most proteins interacting with PCNA have a common binding motif: PCNA interacting protein box (PIP box). However, some proteins with non-canonical PIP-box have also been reported to be the key factors that interacted with PCNA.
Here we discovered the C terminal of a chromatin-remodeling factor CHR721 with non-canonical PIP-box was essential for interacting with OsPCNA in rice. Both OsPCNA and CHR721 were localized in the nuclei and function in response to DNA damages.
Based on the results and previous work, we proposed a working model that CHR721 with non-canonical PIP-box interacted with OsPCNA and both of them probably participate in the DNA damage repair process. |
doi_str_mv | 10.1186/s12870-022-03532-w |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_f64edb9a58b548669b34f27ea8b19389</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_f64edb9a58b548669b34f27ea8b19389</doaj_id><sourcerecordid>2646718254</sourcerecordid><originalsourceid>FETCH-LOGICAL-c426t-fcfcc469297bec5e1f9301a054741c5c1e947275d5402f743dbb9071e814d2e03</originalsourceid><addsrcrecordid>eNpdkk9vFCEYh4nR2Fr9Ah7MJF68oMDw92LSTLTdpLGbRk8eCMO8s8tmZqgw6-q3L-3UpvUC5OXhCfD-EHpLyUdKtfyUKdOKYMIYJrWoGT48Q8eUK4oZY-b5o_URepXzjhCqNDcv0VGhpSDaHKOfzTbF0c1hwgnG2MEQpk3VOz_HVDXnV4rR6hDmbTXFCXtXxuDdUK1Xa9zGP1WYZkgFzgt0mdfNt9NSra6Ch9foRe-GDG_u5xP04-uX7805vrg8WzWnF9hzJmfc-957Lg0zqgUvgPamJtQRwRWnXngKhiumRCc4Yb3idde2higKmvKOAalP0GrxdtHt7HUKo0t_bXTB3hVi2liX5uAHsL3k0LXGCd0KrqU0bc17psDplppam-L6vLiu9-0InYdpTm54In26M4Wt3cTfVhvFibwVfLgXpPhrD3m2Y8gehsFNEPfZMsmlopoJXtD3_6G7uE9T-apCidI2qVRdKLZQPsWcE_QPl6HE3ubALjmwJQf2Lgf2UA69e_yMhyP_Gl_fAAF-rNE</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2652296773</pqid></control><display><type>article</type><title>Chromatin-remodeling factor CHR721 with non-canonical PIP-box interacts with OsPCNA in Rice</title><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><source>PubMed Central (Open access)</source><creator>Zhang, Yushun ; Chen, Qiong ; Zhu, Guanlin ; Zhang, Dechun ; Liang, Weihong</creator><creatorcontrib>Zhang, Yushun ; Chen, Qiong ; Zhu, Guanlin ; Zhang, Dechun ; Liang, Weihong</creatorcontrib><description>Proliferating cell nuclear antigen (PCNA) is one of the key factors for the DNA replication process and DNA damage repair. Most proteins interacting with PCNA have a common binding motif: PCNA interacting protein box (PIP box). However, some proteins with non-canonical PIP-box have also been reported to be the key factors that interacted with PCNA.
Here we discovered the C terminal of a chromatin-remodeling factor CHR721 with non-canonical PIP-box was essential for interacting with OsPCNA in rice. Both OsPCNA and CHR721 were localized in the nuclei and function in response to DNA damages.
Based on the results and previous work, we proposed a working model that CHR721 with non-canonical PIP-box interacted with OsPCNA and both of them probably participate in the DNA damage repair process.</description><identifier>ISSN: 1471-2229</identifier><identifier>EISSN: 1471-2229</identifier><identifier>DOI: 10.1186/s12870-022-03532-w</identifier><identifier>PMID: 35365089</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Amino acids ; Antigens ; Cell cycle ; CHR721 ; Chromatin ; Chromatin remodeling ; Chromatin-remodeling factor ; Cloning ; Cyclin-dependent kinases ; Damage localization ; Deoxyribonucleic acid ; DNA ; DNA biosynthesis ; DNA Damage ; DNA Repair ; Hypotheses ; Kinases ; Mutation ; Oryza - genetics ; OsPCNA ; PIP box ; Proliferating cell nuclear antigen ; Proteins ; Repair ; Transcription Factors</subject><ispartof>BMC plant biology, 2022-04, Vol.22 (1), p.164-164, Article 164</ispartof><rights>2022. The Author(s).</rights><rights>2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c426t-fcfcc469297bec5e1f9301a054741c5c1e947275d5402f743dbb9071e814d2e03</citedby><cites>FETCH-LOGICAL-c426t-fcfcc469297bec5e1f9301a054741c5c1e947275d5402f743dbb9071e814d2e03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8974069/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2652296773?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35365089$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Yushun</creatorcontrib><creatorcontrib>Chen, Qiong</creatorcontrib><creatorcontrib>Zhu, Guanlin</creatorcontrib><creatorcontrib>Zhang, Dechun</creatorcontrib><creatorcontrib>Liang, Weihong</creatorcontrib><title>Chromatin-remodeling factor CHR721 with non-canonical PIP-box interacts with OsPCNA in Rice</title><title>BMC plant biology</title><addtitle>BMC Plant Biol</addtitle><description>Proliferating cell nuclear antigen (PCNA) is one of the key factors for the DNA replication process and DNA damage repair. Most proteins interacting with PCNA have a common binding motif: PCNA interacting protein box (PIP box). However, some proteins with non-canonical PIP-box have also been reported to be the key factors that interacted with PCNA.
Here we discovered the C terminal of a chromatin-remodeling factor CHR721 with non-canonical PIP-box was essential for interacting with OsPCNA in rice. Both OsPCNA and CHR721 were localized in the nuclei and function in response to DNA damages.
Based on the results and previous work, we proposed a working model that CHR721 with non-canonical PIP-box interacted with OsPCNA and both of them probably participate in the DNA damage repair process.</description><subject>Amino acids</subject><subject>Antigens</subject><subject>Cell cycle</subject><subject>CHR721</subject><subject>Chromatin</subject><subject>Chromatin remodeling</subject><subject>Chromatin-remodeling factor</subject><subject>Cloning</subject><subject>Cyclin-dependent kinases</subject><subject>Damage localization</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA biosynthesis</subject><subject>DNA Damage</subject><subject>DNA Repair</subject><subject>Hypotheses</subject><subject>Kinases</subject><subject>Mutation</subject><subject>Oryza - genetics</subject><subject>OsPCNA</subject><subject>PIP box</subject><subject>Proliferating cell nuclear antigen</subject><subject>Proteins</subject><subject>Repair</subject><subject>Transcription Factors</subject><issn>1471-2229</issn><issn>1471-2229</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkk9vFCEYh4nR2Fr9Ah7MJF68oMDw92LSTLTdpLGbRk8eCMO8s8tmZqgw6-q3L-3UpvUC5OXhCfD-EHpLyUdKtfyUKdOKYMIYJrWoGT48Q8eUK4oZY-b5o_URepXzjhCqNDcv0VGhpSDaHKOfzTbF0c1hwgnG2MEQpk3VOz_HVDXnV4rR6hDmbTXFCXtXxuDdUK1Xa9zGP1WYZkgFzgt0mdfNt9NSra6Ch9foRe-GDG_u5xP04-uX7805vrg8WzWnF9hzJmfc-957Lg0zqgUvgPamJtQRwRWnXngKhiumRCc4Yb3idde2higKmvKOAalP0GrxdtHt7HUKo0t_bXTB3hVi2liX5uAHsL3k0LXGCd0KrqU0bc17psDplppam-L6vLiu9-0InYdpTm54In26M4Wt3cTfVhvFibwVfLgXpPhrD3m2Y8gehsFNEPfZMsmlopoJXtD3_6G7uE9T-apCidI2qVRdKLZQPsWcE_QPl6HE3ubALjmwJQf2Lgf2UA69e_yMhyP_Gl_fAAF-rNE</recordid><startdate>20220401</startdate><enddate>20220401</enddate><creator>Zhang, Yushun</creator><creator>Chen, Qiong</creator><creator>Zhu, Guanlin</creator><creator>Zhang, Dechun</creator><creator>Liang, Weihong</creator><general>BioMed Central</general><general>BMC</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>3V.</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20220401</creationdate><title>Chromatin-remodeling factor CHR721 with non-canonical PIP-box interacts with OsPCNA in Rice</title><author>Zhang, Yushun ; Chen, Qiong ; Zhu, Guanlin ; Zhang, Dechun ; Liang, Weihong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c426t-fcfcc469297bec5e1f9301a054741c5c1e947275d5402f743dbb9071e814d2e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Amino acids</topic><topic>Antigens</topic><topic>Cell cycle</topic><topic>CHR721</topic><topic>Chromatin</topic><topic>Chromatin remodeling</topic><topic>Chromatin-remodeling factor</topic><topic>Cloning</topic><topic>Cyclin-dependent kinases</topic><topic>Damage localization</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA biosynthesis</topic><topic>DNA Damage</topic><topic>DNA Repair</topic><topic>Hypotheses</topic><topic>Kinases</topic><topic>Mutation</topic><topic>Oryza - genetics</topic><topic>OsPCNA</topic><topic>PIP box</topic><topic>Proliferating cell nuclear antigen</topic><topic>Proteins</topic><topic>Repair</topic><topic>Transcription Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Yushun</creatorcontrib><creatorcontrib>Chen, Qiong</creatorcontrib><creatorcontrib>Zhu, Guanlin</creatorcontrib><creatorcontrib>Zhang, Dechun</creatorcontrib><creatorcontrib>Liang, Weihong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMC plant biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Yushun</au><au>Chen, Qiong</au><au>Zhu, Guanlin</au><au>Zhang, Dechun</au><au>Liang, Weihong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chromatin-remodeling factor CHR721 with non-canonical PIP-box interacts with OsPCNA in Rice</atitle><jtitle>BMC plant biology</jtitle><addtitle>BMC Plant Biol</addtitle><date>2022-04-01</date><risdate>2022</risdate><volume>22</volume><issue>1</issue><spage>164</spage><epage>164</epage><pages>164-164</pages><artnum>164</artnum><issn>1471-2229</issn><eissn>1471-2229</eissn><abstract>Proliferating cell nuclear antigen (PCNA) is one of the key factors for the DNA replication process and DNA damage repair. Most proteins interacting with PCNA have a common binding motif: PCNA interacting protein box (PIP box). However, some proteins with non-canonical PIP-box have also been reported to be the key factors that interacted with PCNA.
Here we discovered the C terminal of a chromatin-remodeling factor CHR721 with non-canonical PIP-box was essential for interacting with OsPCNA in rice. Both OsPCNA and CHR721 were localized in the nuclei and function in response to DNA damages.
Based on the results and previous work, we proposed a working model that CHR721 with non-canonical PIP-box interacted with OsPCNA and both of them probably participate in the DNA damage repair process.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>35365089</pmid><doi>10.1186/s12870-022-03532-w</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1471-2229 |
ispartof | BMC plant biology, 2022-04, Vol.22 (1), p.164-164, Article 164 |
issn | 1471-2229 1471-2229 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_f64edb9a58b548669b34f27ea8b19389 |
source | Publicly Available Content Database (Proquest) (PQ_SDU_P3); PubMed Central (Open access) |
subjects | Amino acids Antigens Cell cycle CHR721 Chromatin Chromatin remodeling Chromatin-remodeling factor Cloning Cyclin-dependent kinases Damage localization Deoxyribonucleic acid DNA DNA biosynthesis DNA Damage DNA Repair Hypotheses Kinases Mutation Oryza - genetics OsPCNA PIP box Proliferating cell nuclear antigen Proteins Repair Transcription Factors |
title | Chromatin-remodeling factor CHR721 with non-canonical PIP-box interacts with OsPCNA in Rice |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T08%3A19%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Chromatin-remodeling%20factor%20CHR721%20with%20non-canonical%20PIP-box%20interacts%20with%20OsPCNA%20in%20Rice&rft.jtitle=BMC%20plant%20biology&rft.au=Zhang,%20Yushun&rft.date=2022-04-01&rft.volume=22&rft.issue=1&rft.spage=164&rft.epage=164&rft.pages=164-164&rft.artnum=164&rft.issn=1471-2229&rft.eissn=1471-2229&rft_id=info:doi/10.1186/s12870-022-03532-w&rft_dat=%3Cproquest_doaj_%3E2646718254%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c426t-fcfcc469297bec5e1f9301a054741c5c1e947275d5402f743dbb9071e814d2e03%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2652296773&rft_id=info:pmid/35365089&rfr_iscdi=true |