Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
A major locus Qfcr.cau-1B conferring resistance to Fusarium crown rot was identified and validated. The putative gene underlying this locus was pinpointed via virus-induced gene silencing. Fusarium crown rot (FCR), caused by various Fusarium pathogens such as Fusarium pseudograminearum and F. culmorum, is a severe soil-borne disease which significantly affected wheat (Triticum aestivum) production in many arid and semi-arid cropping regions of the world. In this study, a total of 5 QTLs associated with FCR resistance were detected on chromosomes 1B, 2B, 3A, 5A, and 7D using a population of 120 F recombinant inbred lines (RIL) derived from a cross between two Chinese germplasm 20828 and SY95-71. A major locus Qfcr.cau-1B, which accounted for up to 28.33% of the phenotypic variation with a LOD value of 10.99, was consistently detected across all three trials conducted. The effect of Qfcr.cau-1B on FCR resistance was further validated using a F RIL population between 20828 and BLS2. Integrated transcriptome and sequence variation analysis showed that three genes including TraesCS1B02G017700, TraesCS1B02G016400, and TraesCS1B02G022300 were potential candidate genes for Qfcr.cau-1B. Of these three genes, the virus-induced silencing of TraesCS1B02G022300 significantly promoted FCR severity, indicating its positive role in FCR resistance. Taken together, results from this study expand our understanding on genetic basis of FCR resistance in wheat and will be indicative for cloning genes conferring FCR resistance.
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Source |
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http://dx.doi.org/10.1007/s00122-025-04818-x | DOI Listing |
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