Transcriptomics and metabolomics reveal tolerance new mechanism of rice roots to Al stress
The prevalence of soluble aluminum (Al) ions is one of the major limitations to crop production worldwide on acid soils. Therefore, understanding the Al tolerance mechanism of rice and applying Al tolerance functional genes in sensitive plants can significantly improve Al stress resistance. In this...
Saved in:
Published in | Frontiers in genetics Vol. 13; p. 1063984 |
---|---|
Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
10.01.2023
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | The prevalence of soluble aluminum (Al) ions is one of the major limitations to crop production worldwide on acid soils. Therefore, understanding the Al tolerance mechanism of rice and applying Al tolerance functional genes in sensitive plants can significantly improve Al stress resistance. In this study, transcriptomics and metabolomics analyses were performed to reveal the mechanism of Al tolerance differences between two rice landraces (Al-tolerant genotype Shibanzhan (KR) and Al-sensitive genotype Hekedanuo (MR) with different Al tolerance. The results showed that DEG related to phenylpropanoid biosynthesis was highly enriched in KR and MR after Al stress, indicating that phenylpropanoid biosynthesis may be closely related to Al tolerance. E1.11.1.7 (peroxidase) was the most significant enzyme of phenylpropanoid biosynthesis in KR and MR under Al stress and is regulated by multiple genes. We further identified that two candidate genes
Os02g0770800
and
Os06g0521900
may be involved in the regulation of Al tolerance in rice. Our results not only reveal the resistance mechanism of rice to Al stress to some extent, but also provide a useful reference for the molecular mechanism of different effects of Al poisoning on plants. |
---|---|
AbstractList | The prevalence of soluble aluminum (Al) ions is one of the major limitations to crop production worldwide on acid soils. Therefore, understanding the Al tolerance mechanism of rice and applying Al tolerance functional genes in sensitive plants can significantly improve Al stress resistance. In this study, transcriptomics and metabolomics analyses were performed to reveal the mechanism of Al tolerance differences between two rice landraces (Al-tolerant genotype Shibanzhan (KR) and Al-sensitive genotype Hekedanuo (MR) with different Al tolerance. The results showed that DEG related to phenylpropanoid biosynthesis was highly enriched in KR and MR after Al stress, indicating that phenylpropanoid biosynthesis may be closely related to Al tolerance. E1.11.1.7 (peroxidase) was the most significant enzyme of phenylpropanoid biosynthesis in KR and MR under Al stress and is regulated by multiple genes. We further identified that two candidate genes
Os02g0770800
and
Os06g0521900
may be involved in the regulation of Al tolerance in rice. Our results not only reveal the resistance mechanism of rice to Al stress to some extent, but also provide a useful reference for the molecular mechanism of different effects of Al poisoning on plants. The prevalence of soluble aluminum (Al) ions is one of the major limitations to crop production worldwide on acid soils. Therefore, understanding the Al tolerance mechanism of rice and applying Al tolerance functional genes in sensitive plants can significantly improve Al stress resistance. In this study, transcriptomics and metabolomics analyses were performed to reveal the mechanism of Al tolerance differences between two rice landraces (Al-tolerant genotype Shibanzhan (KR) and Al-sensitive genotype Hekedanuo (MR) with different Al tolerance. The results showed that DEG related to phenylpropanoid biosynthesis was highly enriched in KR and MR after Al stress, indicating that phenylpropanoid biosynthesis may be closely related to Al tolerance. E1.11.1.7 (peroxidase) was the most significant enzyme of phenylpropanoid biosynthesis in KR and MR under Al stress and is regulated by multiple genes. We further identified that two candidate genes Os02g0770800 and Os06g0521900 may be involved in the regulation of Al tolerance in rice. Our results not only reveal the resistance mechanism of rice to Al stress to some extent, but also provide a useful reference for the molecular mechanism of different effects of Al poisoning on plants.The prevalence of soluble aluminum (Al) ions is one of the major limitations to crop production worldwide on acid soils. Therefore, understanding the Al tolerance mechanism of rice and applying Al tolerance functional genes in sensitive plants can significantly improve Al stress resistance. In this study, transcriptomics and metabolomics analyses were performed to reveal the mechanism of Al tolerance differences between two rice landraces (Al-tolerant genotype Shibanzhan (KR) and Al-sensitive genotype Hekedanuo (MR) with different Al tolerance. The results showed that DEG related to phenylpropanoid biosynthesis was highly enriched in KR and MR after Al stress, indicating that phenylpropanoid biosynthesis may be closely related to Al tolerance. E1.11.1.7 (peroxidase) was the most significant enzyme of phenylpropanoid biosynthesis in KR and MR under Al stress and is regulated by multiple genes. We further identified that two candidate genes Os02g0770800 and Os06g0521900 may be involved in the regulation of Al tolerance in rice. Our results not only reveal the resistance mechanism of rice to Al stress to some extent, but also provide a useful reference for the molecular mechanism of different effects of Al poisoning on plants. The prevalence of soluble aluminum (Al) ions is one of the major limitations to crop production worldwide on acid soils. Therefore, understanding the Al tolerance mechanism of rice and applying Al tolerance functional genes in sensitive plants can significantly improve Al stress resistance. In this study, transcriptomics and metabolomics analyses were performed to reveal the mechanism of Al tolerance differences between two rice landraces (Al-tolerant genotype Shibanzhan (KR) and Al-sensitive genotype Hekedanuo (MR) with different Al tolerance. The results showed that DEG related to phenylpropanoid biosynthesis was highly enriched in KR and MR after Al stress, indicating that phenylpropanoid biosynthesis may be closely related to Al tolerance. E1.11.1.7 (peroxidase) was the most significant enzyme of phenylpropanoid biosynthesis in KR and MR under Al stress and is regulated by multiple genes. We further identified that two candidate genes and may be involved in the regulation of Al tolerance in rice. Our results not only reveal the resistance mechanism of rice to Al stress to some extent, but also provide a useful reference for the molecular mechanism of different effects of Al poisoning on plants. The prevalence of soluble aluminum (Al) ions is one of the major limitations to crop production worldwide on acid soils. Therefore, understanding the Al tolerance mechanism of rice and applying Al tolerance functional genes in sensitive plants can significantly improve Al stress resistance. In this study, transcriptomics and metabolomics analyses were performed to reveal the mechanism of Al tolerance differences between two rice landraces (Al-tolerant genotype Shibanzhan (KR) and Al-sensitive genotype Hekedanuo (MR) with different Al tolerance. The results showed that DEG related to phenylpropanoid biosynthesis was highly enriched in KR and MR after Al stress, indicating that phenylpropanoid biosynthesis may be closely related to Al tolerance. E1.11.1.7 (peroxidase) was the most significant enzyme of phenylpropanoid biosynthesis in KR and MR under Al stress and is regulated by multiple genes. We further identified that two candidate genes Os02g0770800 and Os06g0521900 may be involved in the regulation of Al tolerance in rice. Our results not only reveal the resistance mechanism of rice to Al stress to some extent, but also provide a useful reference for the molecular mechanism of different effects of Al poisoning on plants. |
Author | Cui, Zhibo Huang, Lixiang Wang, Jingbo Feng, Jing Su, Chang Xu, Hai Zhao, Minghui Jiang, Sixu Zhang, Wenzhong Jiang, Linlin Gu, Shuang |
AuthorAffiliation | Rice Research Institute , Collaborative Innovation Center for Genetic Improvement and High Quality and Efficiency Production of Northeast Japonica Rice in China , Shenyang Agricultural University , Shenyang , China |
AuthorAffiliation_xml | – name: Rice Research Institute , Collaborative Innovation Center for Genetic Improvement and High Quality and Efficiency Production of Northeast Japonica Rice in China , Shenyang Agricultural University , Shenyang , China |
Author_xml | – sequence: 1 givenname: Jingbo surname: Wang fullname: Wang, Jingbo – sequence: 2 givenname: Chang surname: Su fullname: Su, Chang – sequence: 3 givenname: Zhibo surname: Cui fullname: Cui, Zhibo – sequence: 4 givenname: Lixiang surname: Huang fullname: Huang, Lixiang – sequence: 5 givenname: Shuang surname: Gu fullname: Gu, Shuang – sequence: 6 givenname: Sixu surname: Jiang fullname: Jiang, Sixu – sequence: 7 givenname: Jing surname: Feng fullname: Feng, Jing – sequence: 8 givenname: Hai surname: Xu fullname: Xu, Hai – sequence: 9 givenname: Wenzhong surname: Zhang fullname: Zhang, Wenzhong – sequence: 10 givenname: Linlin surname: Jiang fullname: Jiang, Linlin – sequence: 11 givenname: Minghui surname: Zhao fullname: Zhao, Minghui |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36704350$$D View this record in MEDLINE/PubMed |
BookMark | eNp9ks1rHCEYxqWkNB_NP9BDmGMvu_VrRudSCCFtFgK9bC65iOO8bgyObtRN6X8f9yMl6aEiKI_P-3tFn1N0FGIAhL4QPGdM9t_sCgLMKaZ0TnDHesk_oBPSdXwmMSVHb_bH6DznR1wH7xlj_BM6Zp3AnLX4BN0vkw7ZJLcucXImNzqMzQRFD9HvhQTPoH1ToodqNdAE-F0d5kEHl6cm2ia5qqYYS66u5tI3uSTI-TP6aLXPcH5Yz9Ddj-vl1c3s9tfPxdXl7cy0jJdZ27I6LRgsqeUdlmTsWzsYaYm2tN5UsJ5xK8bBknZoR23JyLFghlhaVczO0GLPHaN-VOvkJp3-qKid2gkxrZROxRkPStLOEmLqoxnBewOD0GzAnEijuRAcKuv7nrXeDBOMBkJJ2r-Dvj8J7kGt4rPqpSD1nhXw9QBI8WkDuajJZQPe6wBxkxUVAhOKCeuq9eJtr79NXj-nGuTeYFLMOYFVxhVdXNy2dl4RrLZRULsoqG0U1CEKtZT-U_pK_0_RCxnRuPc |
CitedBy_id | crossref_primary_10_3390_agriculture14081307 crossref_primary_10_3390_ijms251910440 crossref_primary_10_1271_kagakutoseibutsu_61_554 crossref_primary_10_1007_s11104_024_07151_2 crossref_primary_10_1016_j_plaphy_2024_109164 crossref_primary_10_1186_s40538_023_00508_2 crossref_primary_10_1016_j_plantsci_2024_112294 crossref_primary_10_3390_plants13131760 crossref_primary_10_1007_s11104_024_06745_0 crossref_primary_10_1186_s12870_024_05298_9 |
Cites_doi | 10.1016/j.plantsci.2011.12.008 10.1007/s001220000472 10.1016/j.foodchem.2020.126170 10.1016/j.jplph.2004.09.011 10.1016/S0074-7696(07)64005-4 10.1074/jbc.M109.092569 10.1104/pp.107.102335 10.3390/plants9111503 10.1105/tpc.108.064543 10.1016/S0065-2113(07)96004-6 10.1007/bf00009558 10.1093/pcp/pcf081 10.1371/journal.pone.0159622 10.1007/bf00197346 10.1007/bf00010728 10.1146/annurev.pp.46.060195.001321 10.1111/j.1365-313X.2011.04757.x 10.1093/pcp/pcw026 10.1186/s12870-020-02443-y 10.1016/j.foodres.2021.110488 10.1016/j.envint.2019.105154 10.1146/annurev-arplant-043014-114822 10.1016/s1360-1385(01)01961-6 10.1016/j.jplph.2017.11.015 10.1111/j.1744-7909.2008.00687.x 10.1146/annurev.arplant.55.031903.141655 10.1104/pp.110.156794 10.1093/pcp/pcu067 10.1146/annurev.cellbio.22.022206.160206 10.1111/sum.12270 10.3389/fpls.2016.01415 10.1104/pp.107.097162 10.1371/journal.pone.0094803 10.1111/j.1399-3054.1993.tb01784.x 10.1146/annurev-arplant-042809-112315 10.1111/j.1365-313x.2003.01991.x 10.1105/tpc.109.070771 10.1111/nph.17812 10.1080/07388551.2021.1874282 10.1104/pp.111.175802 10.1199/tab.0152 10.1093/pcp/41.4.383 10.1007/s11104-014-2073-1 10.1007/s00299-020-02517-z 10.1111/jipb.13054 10.1016/j.gene.2018.06.105 10.1104/pp.110.154872 10.3389/fpls.2021.667458 10.1046/j.1365-313x.1997.11030429.x 10.1016/j.envexpbot.2017.01.005 10.1111/j.1399-3054.1989.tb05609.x 10.1038/nature06608 10.1016/j.plaphy.2020.08.031 10.1016/j.tplants.2012.08.003 10.1002/pld3.120 10.1016/j.scitotenv.2021.149627 10.3389/fpls.2018.01838 10.1093/oxfordjournals.pcp.a029568 10.1080/00380768.2000.10409141 10.1111/j.1744-7909.2010.00892.x 10.3389/fpls.2021.646221 10.1007/s00299-019-02447-5 10.1111/ppl.13353 10.1023/a:1022867416513 |
ContentType | Journal Article |
Copyright | Copyright © 2023 Wang, Su, Cui, Huang, Gu, Jiang, Feng, Xu, Zhang, Jiang and Zhao. Copyright © 2023 Wang, Su, Cui, Huang, Gu, Jiang, Feng, Xu, Zhang, Jiang and Zhao. 2023 Wang, Su, Cui, Huang, Gu, Jiang, Feng, Xu, Zhang, Jiang and Zhao |
Copyright_xml | – notice: Copyright © 2023 Wang, Su, Cui, Huang, Gu, Jiang, Feng, Xu, Zhang, Jiang and Zhao. – notice: Copyright © 2023 Wang, Su, Cui, Huang, Gu, Jiang, Feng, Xu, Zhang, Jiang and Zhao. 2023 Wang, Su, Cui, Huang, Gu, Jiang, Feng, Xu, Zhang, Jiang and Zhao |
DBID | AAYXX CITATION NPM 7X8 5PM DOA |
DOI | 10.3389/fgene.2022.1063984 |
DatabaseName | CrossRef PubMed MEDLINE - Academic PubMed Central (Full Participant titles) DOAJ Directory of Open Access Journals |
DatabaseTitle | CrossRef PubMed MEDLINE - Academic |
DatabaseTitleList | CrossRef MEDLINE - Academic PubMed |
Database_xml | – sequence: 1 dbid: DOA name: DOAJ Directory of Open Access Journals url: https://www.doaj.org/ sourceTypes: Open Website – sequence: 2 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Biology |
DocumentTitleAlternate | Wang et al |
EISSN | 1664-8021 |
ExternalDocumentID | oai_doaj_org_article_826f11c022c749ceb7a3b0418ca4774e PMC9871393 36704350 10_3389_fgene_2022_1063984 |
Genre | Journal Article |
GroupedDBID | 53G 5VS 9T4 AAFWJ AAKDD AAYXX ACGFS ACXDI ADBBV ADRAZ AFPKN ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL BCNDV CITATION DIK EMOBN GROUPED_DOAJ GX1 HYE KQ8 M48 M~E OK1 PGMZT RNS RPM IAO IEA IHR IPNFZ ISR NPM RIG 7X8 5PM |
ID | FETCH-LOGICAL-c534t-553553fec082f46081d95fbc8f1af236773934f7dbf15b5daf1d4073c1f2f7d03 |
IEDL.DBID | M48 |
ISSN | 1664-8021 |
IngestDate | Wed Aug 27 01:16:59 EDT 2025 Thu Aug 21 18:38:44 EDT 2025 Fri Jul 11 09:28:59 EDT 2025 Thu Jan 02 22:53:52 EST 2025 Tue Jul 01 02:19:29 EDT 2025 Thu Apr 24 23:04:47 EDT 2025 |
IsDoiOpenAccess | true |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Keywords | aluminum tolerance transcriptomics internal tolerance rice metabolomics |
Language | English |
License | Copyright © 2023 Wang, Su, Cui, Huang, Gu, Jiang, Feng, Xu, Zhang, Jiang and Zhao. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c534t-553553fec082f46081d95fbc8f1af236773934f7dbf15b5daf1d4073c1f2f7d03 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Reviewed by: Muhammad Aamir Manzoor, Anhui Agricultural University, China Peng Zhang, China National Rice Research Institute (CAAS), China Edited by: Dezhi Wu, Hunan Agricultural University, China Chongyun Fu, Guangdong Academy of Agricultural Sciences (GDAAS), China This article was submitted to Plant Genomics, a section of the journal Frontiers in Genetics |
OpenAccessLink | http://journals.scholarsportal.info/openUrl.xqy?doi=10.3389/fgene.2022.1063984 |
PMID | 36704350 |
PQID | 2770120136 |
PQPubID | 23479 |
ParticipantIDs | doaj_primary_oai_doaj_org_article_826f11c022c749ceb7a3b0418ca4774e pubmedcentral_primary_oai_pubmedcentral_nih_gov_9871393 proquest_miscellaneous_2770120136 pubmed_primary_36704350 crossref_citationtrail_10_3389_fgene_2022_1063984 crossref_primary_10_3389_fgene_2022_1063984 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2023-01-10 |
PublicationDateYYYYMMDD | 2023-01-10 |
PublicationDate_xml | – month: 01 year: 2023 text: 2023-01-10 day: 10 |
PublicationDecade | 2020 |
PublicationPlace | Switzerland |
PublicationPlace_xml | – name: Switzerland |
PublicationTitle | Frontiers in genetics |
PublicationTitleAlternate | Front Genet |
PublicationYear | 2023 |
Publisher | Frontiers Media S.A |
Publisher_xml | – name: Frontiers Media S.A |
References | Kochian (B26) 1995; 46 Hiradate (B19) 2007; 96 Ma (B36) 2014; 381 Kobayashi (B25) 2007; 145 Ma (B39) 2002; 43 Yokosho (B68) 2011; 68 Huang (B20) 2009; 21 Sharma (B52) 2005; 162 Kochian (B28) 2015; 66 Clemens (B8) 2013; 18 Nguyen (B44) 2001; 102 Pellet (B46) 1995; 196 Moura (B43) 2010; 52 Sasaki (B50) 2004; 37 Zhang J (B69) 2016; 11 Konno (B29) 1993; 89 Ma (B37) 2000; 41 Fraser (B14) 2011; 9 Koyama (B30) 1999; 40 Ishikawa (B21) 2000; 46 Goulding (B17) 2016; 32 Yang (B66) 2008; 50 Kiani (B24) 2021; 12 Dong (B9) 2021; 63 Ma (B38) 2001; 6 Zhao (B71) 2018; 9 Durrett (B11) 2007; 144 Dopico (B10) 1989; 75 Rose (B48) 2010; 153 von Uexkull (B60) 1995; 171 Zhang, P (B70) 2016; 7 Preisner (B47) 2018; 221 Bartsch (B2) 2010; 13 Ninamango-Cárdenas (B45) 2003; 130 Wu (B63) 2014; 55 Lacombe (B31) 1997; 11 Yokosho (B67) 2016; 57 Wohl (B62) 2020; 39 Chen (B7) 2020; 155 Gong (B16) 2020; 20 Somerville (B55) 2006; 22 Ghosh Dasgupta (B15) 2014; 9 Fang (B13) 2021; 12 Yang (B65) 2020; 314 Bennet (B3) 1991; 134 Chen (B6) 2019; 133 Zhu (B73) 2022; 233 Chauhan (B4) 2021; 41 Gray (B18) 2012; 184 Yamaji (B64) 2009; 21 Scheller (B51) 2010; 61 Tsutsui (B57) 2011; 156 Ke (B22) 2018; 675 Li (B33) 2021; 172 Kochian (B27) 2004; 55 Matsunami (B42) 2020; 9 Shweta (B53) 2017; 137 Vives-Peris (B59) 2020; 39 Famoso (B12) 2010; 153 Solhaug (B54) 2019; 3 Wang (B61) 2021; 800 Ma (B40) 2007; 264 Vahisalu (B58) 2008; 452 Ruiz de la Bastida (B49) 2021; 147 |
References_xml | – volume: 184 start-page: 112 year: 2012 ident: B18 article-title: Grass phenylpropanoids: Regulate before using publication-title: Plant Sci. doi: 10.1016/j.plantsci.2011.12.008 – volume: 102 start-page: 1002 year: 2001 ident: B44 article-title: Molecular mapping of genes conferring aluminum tolerance in rice (Oryza sativa L.) publication-title: Theor. Appl. Genet. doi: 10.1007/s001220000472 – volume: 314 start-page: 126170 year: 2020 ident: B65 article-title: Transcriptomics integrated with metabolomics reveals the effect of regulated deficit irrigation on anthocyanin biosynthesis in Cabernet Sauvignon grape berries publication-title: Food Chem. doi: 10.1016/j.foodchem.2020.126170 – volume: 162 start-page: 854 year: 2005 ident: B52 article-title: Modulation of nitrate reductase activity in rice seedlings under aluminium toxicity and water stress: Role of osmolytes as enzyme protectant publication-title: J. Plant Physiol. doi: 10.1016/j.jplph.2004.09.011 – volume: 264 start-page: 225 year: 2007 ident: B40 article-title: Syndrome of aluminum toxicity and diversity of aluminum resistance in higher plants publication-title: Int. Rev. Cytol. doi: 10.1016/S0074-7696(07)64005-4 – volume: 13 start-page: 25654 year: 2010 ident: B2 article-title: Accumulation of isochorismate-derived 2,3-dihydroxybenzoic 3-O-beta-D-xyloside in arabidopsis resistance to pathogens and ageing of leaves publication-title: J. Biol. Chem. doi: 10.1074/jbc.M109.092569 – volume: 145 start-page: 843 year: 2007 ident: B25 article-title: Characterization of AtALMT1 expression in aluminum-inducible malate release and its role for rhizotoxic stress tolerance in arabidopsis publication-title: Plant Physiol. doi: 10.1104/pp.107.102335 – volume: 9 start-page: 1503 year: 2020 ident: B42 article-title: Osmotic stress leads to significant changes in rice root metabolic profiles between tolerant and sensitive genotypes publication-title: Plants (Basel) doi: 10.3390/plants9111503 – volume: 21 start-page: 655 year: 2009 ident: B20 article-title: A bacterial-type ABC transporter is involved in aluminum tolerance in rice publication-title: Plant Cell. doi: 10.1105/tpc.108.064543 – volume: 96 start-page: 65 year: 2007 ident: B19 article-title: Strategies of plants to adapt to mineral stresses in problem soils publication-title: Adv. Agron. doi: 10.1016/S0065-2113(07)96004-6 – volume: 171 start-page: 1 year: 1995 ident: B60 article-title: Global extent, development and economic-impact of acid soils publication-title: Plant Soil doi: 10.1007/bf00009558 – volume: 43 start-page: 652 year: 2002 ident: B39 article-title: Response of rice to Al stress and identification of quantitative trait loci for Al tolerance publication-title: Plant Cell. Physiol. doi: 10.1093/pcp/pcf081 – volume: 11 start-page: e0159622 year: 2016 ident: B69 article-title: Metabolic profiles reveal changes in wild and cultivated soybean seedling leaves under salt stress publication-title: PLoS One doi: 10.1371/journal.pone.0159622 – volume: 196 start-page: 788 year: 1995 ident: B46 article-title: Organic acid exudation as an aluminum-tolerance mechanism in maize (Zea mays L.) publication-title: Planta doi: 10.1007/bf00197346 – volume: 134 start-page: 153 year: 1991 ident: B3 article-title: The aluminium signal: New dimensions to mechanisms of aluminium tolerance publication-title: Plant Soil doi: 10.1007/bf00010728 – volume: 46 start-page: 237 year: 1995 ident: B26 article-title: Cellular mechanisms of aluminum toxicity and resistance in plants publication-title: Annu. Rev. Plant Biol. doi: 10.1146/annurev.pp.46.060195.001321 – volume: 68 start-page: 1061 year: 2011 ident: B68 article-title: An Al-inducible MATE gene is involved in external detoxification of Al in rice publication-title: Plant J. doi: 10.1111/j.1365-313X.2011.04757.x – volume: 57 start-page: 976 year: 2016 ident: B67 article-title: Functional analysis of a MATE gene OsFRDL2 revealed its involvement in Al-induced secretion of citrate, but less contribution to Al tolerance in rice publication-title: Plant Cell. Physiol. doi: 10.1093/pcp/pcw026 – volume: 20 start-page: 294 year: 2020 ident: B16 article-title: Integrated transcriptomics and metabolomics analysis of catechins, caffeine and theanine biosynthesis in tea plant (Camellia sinensis) over the course of seasons publication-title: BMC Plant Biol. doi: 10.1186/s12870-020-02443-y – volume: 147 start-page: 110488 year: 2021 ident: B49 article-title: Metabolism of flavonoids and lignans by lactobacilli and bifidobacteria strains improves the nutritional properties of flaxseed-enriched beverages publication-title: Food Res. Int. doi: 10.1016/j.foodres.2021.110488 – volume: 133 start-page: 105154 year: 2019 ident: B6 article-title: Metabolomics and transcriptomics reveal defense mechanism of rice (Oryza sativa) grains under stress of 2, 2’, 4, 4’-tetrabromodiphenyl ether publication-title: Environ. Int. doi: 10.1016/j.envint.2019.105154 – volume: 66 start-page: 571 year: 2015 ident: B28 article-title: Plant adaptation to acid soils: The molecular basis for crop aluminum resistance publication-title: Annu. Rev. Plant Biol. doi: 10.1146/annurev-arplant-043014-114822 – volume: 6 start-page: 273 year: 2001 ident: B38 article-title: Aluminium tolerance in plants and the complexing role of organic acids publication-title: Trends Plant Sci. doi: 10.1016/s1360-1385(01)01961-6 – volume: 221 start-page: 132 year: 2018 ident: B47 article-title: The cinnamyl alcohol dehydrogenase family in flax: Differentiation during plant growth and under stress conditions publication-title: J. Plant Physiol. doi: 10.1016/j.jplph.2017.11.015 – volume: 50 start-page: 1103 year: 2008 ident: B66 article-title: Aluminum-activated oxalate secretion does not associate with internal content among some oxalate accumulators publication-title: J. Integr. Plant Biol. doi: 10.1111/j.1744-7909.2008.00687.x – volume: 55 start-page: 459 year: 2004 ident: B27 article-title: How do crop plants tolerate acid soils? Mechanisms of aluminum tolerance and phosphorous efficiency publication-title: Annu. Rev. Plant Biol. doi: 10.1146/annurev.arplant.55.031903.141655 – volume: 153 start-page: 1678 year: 2010 ident: B12 article-title: Development of a novel aluminum tolerance phenotyping platform used for comparisons of cereal aluminum tolerance and investigations into rice aluminum tolerance mechanisms publication-title: Plant Physiol. doi: 10.1104/pp.110.156794 – volume: 55 start-page: 1426 year: 2014 ident: B63 article-title: Brassica oleracea MATE encodes a citrate transporter and enhances aluminum tolerance in Arabidopsis thaliana publication-title: Plant Cell. Physiol. doi: 10.1093/pcp/pcu067 – volume: 22 start-page: 53 year: 2006 ident: B55 article-title: Cellulose synthesis in higher plants publication-title: Annu. Rev. Cell. Dev. Biol. doi: 10.1146/annurev.cellbio.22.022206.160206 – volume: 32 start-page: 390 year: 2016 ident: B17 article-title: Soil acidification and the importance of liming agricultural soils with particular reference to the United Kingdom publication-title: Soil Use Manag. doi: 10.1111/sum.12270 – volume: 7 start-page: 1415 year: 2016 ident: B70 article-title: Association mapping for aluminum tolerance in a core collection of rice landraces publication-title: Front. Plant Sci. doi: 10.3389/fpls.2016.01415 – volume: 144 start-page: 197 year: 2007 ident: B11 article-title: The FRD3-mediated efflux of citrate into the root vasculature is necessary for efficient iron translocation publication-title: Plant Physiol. doi: 10.1104/pp.107.097162 – volume: 9 start-page: e94803 year: 2014 ident: B15 article-title: Characterization of Withania somnifera leaf transcriptome and expression analysis of pathogenesis-related genes during salicylic acid signaling publication-title: PLoS One doi: 10.1371/journal.pone.0094803 – volume: 89 start-page: 40 year: 1993 ident: B29 article-title: Purification of a β-galactosidase from rice shoots and its involvement in hydrolysis of the natural substrate in cell walls publication-title: Physiol. Plant doi: 10.1111/j.1399-3054.1993.tb01784.x – volume: 61 start-page: 263 year: 2010 ident: B51 article-title: Hemicelluloses publication-title: Annu.rev.plant Biol. doi: 10.1146/annurev-arplant-042809-112315 – volume: 37 start-page: 645 year: 2004 ident: B50 article-title: A wheat gene encoding an aluminum-activated malate transporter publication-title: Plant J doi: 10.1111/j.1365-313x.2003.01991.x – volume: 21 start-page: 3339 year: 2009 ident: B64 article-title: A zinc finger transcription factor ART1 regulates multiple genes implicated in aluminum tolerance in rice publication-title: Plant Cell. doi: 10.1105/tpc.109.070771 – volume: 233 start-page: 2471 year: 2022 ident: B73 article-title: Calmodulin-like protein CML24 interacts with CAMTA2 and WRKY46 to regulate ALMT1-dependent Al resistance in Arabidopsis thaliana publication-title: New Phytol. doi: 10.1111/nph.17812 – volume: 41 start-page: 715 year: 2021 ident: B4 article-title: Aluminum toxicity and aluminum stress-induced physiological tolerance responses in higher plants publication-title: Crit. Rev. Biotechnol. doi: 10.1080/07388551.2021.1874282 – volume: 156 start-page: 925 year: 2011 ident: B57 article-title: Identification of a cis-acting element of ART1, a C2H2-type zinc-finger transcription factor for aluminum tolerance in rice publication-title: Plant Physiol. doi: 10.1104/pp.111.175802 – volume: 9 start-page: e0152 year: 2011 ident: B14 article-title: The phenylpropanoid pathway in Arabidopsis publication-title: Arab. Book doi: 10.1199/tab.0152 – volume: 41 start-page: 383 year: 2000 ident: B37 article-title: Role of organic acids in detoxification of aluminum in higher plants publication-title: Plant Cell. Physiol. doi: 10.1093/pcp/41.4.383 – volume: 381 start-page: 1 year: 2014 ident: B36 article-title: Molecular mechanisms of Al tolerance in gramineous plants publication-title: Plant Soil doi: 10.1007/s11104-014-2073-1 – volume: 39 start-page: 597 year: 2020 ident: B62 article-title: Functional expression and characterization of cinnamic acid 4-hydroxylase from the hornwort Anthoceros agrestis in Physcomitrella patens publication-title: Plant Cell. Rep. doi: 10.1007/s00299-020-02517-z – volume: 63 start-page: 180 year: 2021 ident: B9 article-title: Contribution of phenylpropanoid metabolism to plant development and plant-environment interactions publication-title: J. Integr. Plant Biol. doi: 10.1111/jipb.13054 – volume: 675 start-page: 285 year: 2018 ident: B22 article-title: Genome-wide transcriptome profiling provides insights into panicle development of rice (Oryza sativa L.) publication-title: Gene-Basel. doi: 10.1016/j.gene.2018.06.105 – volume: 153 start-page: 433 year: 2010 ident: B48 article-title: Straying off the highway: Trafficking of secreted plant proteins and complexity in the plant cell wall proteome publication-title: Plant Physiol. doi: 10.1104/pp.110.154872 – volume: 12 start-page: 667458 year: 2021 ident: B13 article-title: Response mechanisms of plants under saline-alkali stress publication-title: Front. Plant Sci. doi: 10.3389/fpls.2021.667458 – volume: 11 start-page: 429 year: 1997 ident: B31 article-title: Cinnamoyl CoA reductase, the first committed enzyme of the lignin branch biosynthetic pathway: Cloning, expression and phylogenetic relationships publication-title: Plant J. doi: 10.1046/j.1365-313x.1997.11030429.x – volume: 137 start-page: 177 year: 2017 ident: B53 article-title: Toxicity of aluminium on various levels of plant cells and organism: A review publication-title: Environ. Exp. Bot. doi: 10.1016/j.envexpbot.2017.01.005 – volume: 75 start-page: 458 year: 1989 ident: B10 article-title: Partial purification of cell wall beta-galactosidases from Cicer arietinum epicotyls. Relationship with cell wall autolytic processes publication-title: Plant Physiol. doi: 10.1111/j.1399-3054.1989.tb05609.x – volume: 452 start-page: 487 year: 2008 ident: B58 article-title: SLAC1 is required for plant guard cell S-type anion channel function in stomatal signalling publication-title: Nature doi: 10.1038/nature06608 – volume: 155 start-page: 697 year: 2020 ident: B7 article-title: Fraxinus mandshurica 4-coumarate-CoA ligase 2 enhances drought and osmotic stress tolerance of tobacco by increasing coniferyl alcohol content publication-title: Plant Physiol. Biochem. doi: 10.1016/j.plaphy.2020.08.031 – volume: 18 start-page: 92 year: 2013 ident: B8 article-title: Plant science: The key to preventing slow cadmium poisoning publication-title: Trends Plant Sci. doi: 10.1016/j.tplants.2012.08.003 – volume: 3 start-page: e00120 year: 2019 ident: B54 article-title: An integrated transcriptomics and metabolomics analysis of the Cucurbita pepo nectary implicates key modules of primary metabolism involved in nectar synthesis and secretion publication-title: Plant Direct doi: 10.1002/pld3.120 – volume: 800 start-page: 149627 year: 2021 ident: B61 article-title: Nanobubbles promote nutrient utilization and plant growth in rice by upregulating nutrient uptake genes and stimulating growth hormone production publication-title: Sci. Total Environ. doi: 10.1016/j.scitotenv.2021.149627 – volume: 9 start-page: 1838 year: 2018 ident: B71 article-title: Mining beneficial genes for aluminum tolerance within a core collection of rice landraces through genome-wide association mapping with high density SNPs from specific-locus amplified fragment sequencing publication-title: Front. Plant Sci. doi: 10.3389/fpls.2018.01838 – volume: 40 start-page: 482 year: 1999 ident: B30 article-title: Over expression of mitochondrial citrate synthase gene improves the growth of carrot cells in Al-phosphate medium publication-title: Plant. Cell. physiology doi: 10.1093/oxfordjournals.pcp.a029568 – volume: 46 start-page: 751 year: 2000 ident: B21 article-title: Comparison of the amount of citric and malic acids in Al media of seven plant species and two cultivars each in five plant species publication-title: Soil Sci. Plant Nutr. doi: 10.1080/00380768.2000.10409141 – volume: 52 start-page: 360 year: 2010 ident: B43 article-title: Abiotic and biotic stresses and changes in the lignin content and composition in plants publication-title: J. Integr. Plant Biol. doi: 10.1111/j.1744-7909.2010.00892.x – volume: 12 start-page: 646221 year: 2021 ident: B24 article-title: Polyphenols, flavonoids, and antioxidant activity involved in salt tolerance in wheat, aegilops cylindrica and their amphidiploids publication-title: Front. Plant Sci. doi: 10.3389/fpls.2021.646221 – volume: 39 start-page: 3 year: 2020 ident: B59 article-title: Root exudates: From plant to rhizosphere and beyond publication-title: Plant Cell. Rep. doi: 10.1007/s00299-019-02447-5 – volume: 172 start-page: 1619 year: 2021 ident: B33 article-title: Myo-inositol transport and metabolism participate in salt tolerance of halophyte ice plant seedlings publication-title: Physiol. Plant doi: 10.1111/ppl.13353 – volume: 130 start-page: 223 year: 2003 ident: B45 article-title: Mapping QTLs for aluminum tolerance in maize publication-title: Euphytica doi: 10.1023/a:1022867416513 |
SSID | ssj0000493334 |
Score | 2.3682992 |
Snippet | The prevalence of soluble aluminum (Al) ions is one of the major limitations to crop production worldwide on acid soils. Therefore, understanding the Al... |
SourceID | doaj pubmedcentral proquest pubmed crossref |
SourceType | Open Website Open Access Repository Aggregation Database Index Database Enrichment Source |
StartPage | 1063984 |
SubjectTerms | aluminum tolerance Genetics internal tolerance metabolomics rice transcriptomics |
SummonAdditionalLinks | – databaseName: DOAJ Directory of Open Access Journals dbid: DOA link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1NT9wwELUqJKReKqAFUqBypd6qaOPYzsdxQSBUCU5dadWLZTseAVqyqJs98O-ZibOrXYTKpVdnklgz48wbx_OGsR8FVEJDXqcebJYqBPipwwWZCl3aqlJKyYb2IW9ui-uJ-jXV041WX3QmLNIDR8WNEP6CEB5DjS9V7YMrrXSZEpW3CqFLoK8vxryNZOoh4l4ppYpVMpiF1SNAexAtZp5jwophuVJbkagn7H8LZb4-LLkRfa722KcBNvJxnO4--xDaA7YbG0k-f2Z_-pDTfwCoynjBbdvwx9ChhWdxgJia8AHdfBaolUbgCKdRgup-7xePfA6c2IU44uhugVJ8POOxjOQLm1xd_r64ToeuCanXUnWp1gghJASPwR1UgSG_qTU4X4GwQHxtxIGnoGwcCO10Y0E0mNVJLyDH0Uwesp123oZjxqWjnLUuXFGC8jpYBFNaFb7OMC2ErEmYWGnQ-IFSnDpbzAymFqR102vdkNbNoPWE_Vzf8xQJNf4pfU6GWUsSGXY_gC5iBhcx77lIwr6vzGpw8dAfEduG-XJh8rKk4mEhi4QdRTOvX0XMdogls4SVWw6wNZftK-39XU_QXWMWikr--j8mf8I-Uod72vUR2Snb6f4uwxnioM59613-BXOiBTA priority: 102 providerName: Directory of Open Access Journals |
Title | Transcriptomics and metabolomics reveal tolerance new mechanism of rice roots to Al stress |
URI | https://www.ncbi.nlm.nih.gov/pubmed/36704350 https://www.proquest.com/docview/2770120136 https://pubmed.ncbi.nlm.nih.gov/PMC9871393 https://doaj.org/article/826f11c022c749ceb7a3b0418ca4774e |
Volume | 13 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Nb9QwEB2VIlAviG_CR2UkbigQx3acHBAqiFIhlRMrrbhEtmNDUZrQTSq1_56ZOLtiUcslB8dxIs84856TeQPwqgglVyGvUhdMlkoE-KnFBZlypU1ZSilFQ_uQx1-Lo4X8slTLHViXO5oncLiS2lE9qcWqfXNxdvkeF_w7YpwYb98GnGpSvMxz5KIYcUt5A25iZNJU0eB4hvu_IhoWIn5oLgqJL-ecxzyaa4bZg9ukb4aIItsKW5O6_1WQ9N8_K_8KVYd34c6MMdlBdIp7sOO7-3ArVp28fADfp_g0vS0oJXlgpmvYqR_RHdrYQLJOOMDYt57qbniG2Bt7UJLwyXDK-sBIiogh6B4H7MUOWhZzTh7C4vDTt49H6VxiIXVKyDFVCvGGCN4hEgiyQHzQVCpYVwZuAom7kWCeDLqxgSurGhN4gxRQOB5ybM3EI9jt-s4_ASYsEdyqsIUO0ilvEHkpWbgqQw4ZsiYBvp7B2s3641QGo62Rh5AB6skANRmgng2QwOvNNb-j-sZ_e38gw2x6knL21NCvftTzQqyRTgXOHV7mtKyct9oIm0leOiMRCvsEXq7NWuNKo88npvP9-VDnWlOmMRdFAo-jmTe3WrtJAnrLAbaeZftMd_JzUvOukLLiJD-9dsxnsEc17mnfh2fPYXdcnfsXiIRGuz_tIODx85LvT67-BwJDBJQ |
linkProvider | Scholars Portal |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Transcriptomics+and+metabolomics+reveal+tolerance+new+mechanism+of+rice+roots+to+Al+stress&rft.jtitle=Frontiers+in+genetics&rft.au=Wang%2C+Jingbo&rft.au=Su%2C+Chang&rft.au=Cui%2C+Zhibo&rft.au=Huang%2C+Lixiang&rft.date=2023-01-10&rft.issn=1664-8021&rft.eissn=1664-8021&rft.volume=13&rft.spage=1063984&rft_id=info:doi/10.3389%2Ffgene.2022.1063984&rft_id=info%3Apmid%2F36704350&rft.externalDocID=36704350 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1664-8021&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1664-8021&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1664-8021&client=summon |