Novel and stable QTL regions conferring resistance to MYMV disease and its inheritance in blackgram (Vignamungo (L.) Hepper)
Mungbean yellow mosaic virus (MYMV) disease is a significant constraint for blackgram production. The present study employed a mapping population derived from a cross between susceptible (MDU 1) and resistant (TU 68) genotypes to identify quantitative trait loci (QTL) associated with MYMV disease re...
Gespeichert in:
Veröffentlicht in: | Journal of genetics 2022, Vol.101 (1), Article 18 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 1 |
container_start_page | |
container_title | Journal of genetics |
container_volume | 101 |
creator | Subramaniyan, Ragul Narayana, Manivannan Krishnamoorthy, Iyanar Natarajan, Ganapathy Gandhi, Karthikeyan |
description | Mungbean yellow mosaic virus (MYMV) disease is a significant constraint for blackgram production. The present study employed a mapping population derived from a cross between susceptible (MDU 1) and resistant (TU 68) genotypes to identify quantitative trait loci (QTL) associated with MYMV disease resistance in addition to bruchine resistance loci identified from the previous study. Phenotyping was carried out in F
2
generation under the disease spreader row method at field condition. Disease score observations were carried out 60 days after sowing (DAS). The chi-square goodness of fit test revealed inhibitory gene action with two genes controlling the expression of resistance to MYMV disease. However, QTL analysis revealed one major QTL region, i.e.
qMYMVD_60
at LG 10 responsible for MYMV disease score at 60 DAS, accounted for 21 per cent of variation. The identified QTL has the flanking markers as CEDG180 and CEDG116. Hence, the QTL,
qMYMVD_60
may be utilized in the breeding of MYMV disease resistance. Further, the marker-assisted introgression of both the MYMV and bruchine resistance QTLs can be performed in the near future. |
doi_str_mv | 10.1007/s12041-022-01359-w |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2634520055</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2633262120</sourcerecordid><originalsourceid>FETCH-LOGICAL-c375t-d5859e404dd03af1e38f83aa8e9e56472d15ebda1d120ca7a45e71da7fdfb9033</originalsourceid><addsrcrecordid>eNp9kc1u1TAUhC0EoqXwAiyQJTa3ixTbJ76-WaIKaKVbEFKpxMpy4pPgktipnVAh8fA4TQsSC1b--2aONUPIS85OOGPqTeKClbxgQhSMg6yK20fkkFUKCqWAP8775YkDwAF5ltL1clRMPCUHIIXgwMUh-fUx_MCeGm9pmkzdI_18uacROxd8ok3wLcbofJevksuEb5BOgV58vbii1iU0Ce_EbkrU-W8Y3co4T-veNN-7aAa6uXKdN8Psu0A3-5NjeobjiPH4OXnSmj7hi_v1iHx5_-7y9KzYf_pwfvp2XzSg5FRYuZMVlqy0loFpOcKu3YExO6xQbkslLJdYW8NtDqQxypQSFbdGtbatKwZwRDar7xjDzYxp0oNLDfa98RjmpMUWSikYkzKjr_9Br8Mcff7dQoHYijwjU2KlmhhSitjqMbrBxJ-aM710o9dudE5c33Wjb7Po1b31XA9o_0geysgArEAal8gx_p39H9vf_AuZvA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2633262120</pqid></control><display><type>article</type><title>Novel and stable QTL regions conferring resistance to MYMV disease and its inheritance in blackgram (Vignamungo (L.) Hepper)</title><source>MEDLINE</source><source>Indian Academy of Sciences</source><source>SpringerLink Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Subramaniyan, Ragul ; Narayana, Manivannan ; Krishnamoorthy, Iyanar ; Natarajan, Ganapathy ; Gandhi, Karthikeyan</creator><creatorcontrib>Subramaniyan, Ragul ; Narayana, Manivannan ; Krishnamoorthy, Iyanar ; Natarajan, Ganapathy ; Gandhi, Karthikeyan</creatorcontrib><description>Mungbean yellow mosaic virus (MYMV) disease is a significant constraint for blackgram production. The present study employed a mapping population derived from a cross between susceptible (MDU 1) and resistant (TU 68) genotypes to identify quantitative trait loci (QTL) associated with MYMV disease resistance in addition to bruchine resistance loci identified from the previous study. Phenotyping was carried out in F
2
generation under the disease spreader row method at field condition. Disease score observations were carried out 60 days after sowing (DAS). The chi-square goodness of fit test revealed inhibitory gene action with two genes controlling the expression of resistance to MYMV disease. However, QTL analysis revealed one major QTL region, i.e.
qMYMVD_60
at LG 10 responsible for MYMV disease score at 60 DAS, accounted for 21 per cent of variation. The identified QTL has the flanking markers as CEDG180 and CEDG116. Hence, the QTL,
qMYMVD_60
may be utilized in the breeding of MYMV disease resistance. Further, the marker-assisted introgression of both the MYMV and bruchine resistance QTLs can be performed in the near future.</description><identifier>ISSN: 0022-1333</identifier><identifier>EISSN: 0973-7731</identifier><identifier>DOI: 10.1007/s12041-022-01359-w</identifier><identifier>PMID: 35221312</identifier><language>eng</language><publisher>New Delhi: Springer India</publisher><subject>Animal Genetics and Genomics ; Biomedical and Life Sciences ; Disease resistance ; Disease Resistance - genetics ; Evolutionary Biology ; Genotypes ; Heredity ; Life Sciences ; Microbial Genetics and Genomics ; Phenotyping ; Plant Breeding ; Plant Diseases - genetics ; Plant Genetics and Genomics ; Population studies ; Quantitative Trait Loci ; Research Article ; Vigna - genetics</subject><ispartof>Journal of genetics, 2022, Vol.101 (1), Article 18</ispartof><rights>Indian Academy of Sciences 2022</rights><rights>Indian Academy of Sciences 2022.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-d5859e404dd03af1e38f83aa8e9e56472d15ebda1d120ca7a45e71da7fdfb9033</citedby><cites>FETCH-LOGICAL-c375t-d5859e404dd03af1e38f83aa8e9e56472d15ebda1d120ca7a45e71da7fdfb9033</cites><orcidid>0000-0001-5918-1799 ; 0000-0003-4448-5196</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12041-022-01359-w$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12041-022-01359-w$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35221312$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Subramaniyan, Ragul</creatorcontrib><creatorcontrib>Narayana, Manivannan</creatorcontrib><creatorcontrib>Krishnamoorthy, Iyanar</creatorcontrib><creatorcontrib>Natarajan, Ganapathy</creatorcontrib><creatorcontrib>Gandhi, Karthikeyan</creatorcontrib><title>Novel and stable QTL regions conferring resistance to MYMV disease and its inheritance in blackgram (Vignamungo (L.) Hepper)</title><title>Journal of genetics</title><addtitle>J Genet</addtitle><addtitle>J Genet</addtitle><description>Mungbean yellow mosaic virus (MYMV) disease is a significant constraint for blackgram production. The present study employed a mapping population derived from a cross between susceptible (MDU 1) and resistant (TU 68) genotypes to identify quantitative trait loci (QTL) associated with MYMV disease resistance in addition to bruchine resistance loci identified from the previous study. Phenotyping was carried out in F
2
generation under the disease spreader row method at field condition. Disease score observations were carried out 60 days after sowing (DAS). The chi-square goodness of fit test revealed inhibitory gene action with two genes controlling the expression of resistance to MYMV disease. However, QTL analysis revealed one major QTL region, i.e.
qMYMVD_60
at LG 10 responsible for MYMV disease score at 60 DAS, accounted for 21 per cent of variation. The identified QTL has the flanking markers as CEDG180 and CEDG116. Hence, the QTL,
qMYMVD_60
may be utilized in the breeding of MYMV disease resistance. Further, the marker-assisted introgression of both the MYMV and bruchine resistance QTLs can be performed in the near future.</description><subject>Animal Genetics and Genomics</subject><subject>Biomedical and Life Sciences</subject><subject>Disease resistance</subject><subject>Disease Resistance - genetics</subject><subject>Evolutionary Biology</subject><subject>Genotypes</subject><subject>Heredity</subject><subject>Life Sciences</subject><subject>Microbial Genetics and Genomics</subject><subject>Phenotyping</subject><subject>Plant Breeding</subject><subject>Plant Diseases - genetics</subject><subject>Plant Genetics and Genomics</subject><subject>Population studies</subject><subject>Quantitative Trait Loci</subject><subject>Research Article</subject><subject>Vigna - genetics</subject><issn>0022-1333</issn><issn>0973-7731</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1u1TAUhC0EoqXwAiyQJTa3ixTbJ76-WaIKaKVbEFKpxMpy4pPgktipnVAh8fA4TQsSC1b--2aONUPIS85OOGPqTeKClbxgQhSMg6yK20fkkFUKCqWAP8775YkDwAF5ltL1clRMPCUHIIXgwMUh-fUx_MCeGm9pmkzdI_18uacROxd8ok3wLcbofJevksuEb5BOgV58vbii1iU0Ce_EbkrU-W8Y3co4T-veNN-7aAa6uXKdN8Psu0A3-5NjeobjiPH4OXnSmj7hi_v1iHx5_-7y9KzYf_pwfvp2XzSg5FRYuZMVlqy0loFpOcKu3YExO6xQbkslLJdYW8NtDqQxypQSFbdGtbatKwZwRDar7xjDzYxp0oNLDfa98RjmpMUWSikYkzKjr_9Br8Mcff7dQoHYijwjU2KlmhhSitjqMbrBxJ-aM710o9dudE5c33Wjb7Po1b31XA9o_0geysgArEAal8gx_p39H9vf_AuZvA</recordid><startdate>2022</startdate><enddate>2022</enddate><creator>Subramaniyan, Ragul</creator><creator>Narayana, Manivannan</creator><creator>Krishnamoorthy, Iyanar</creator><creator>Natarajan, Ganapathy</creator><creator>Gandhi, Karthikeyan</creator><general>Springer India</general><general>Springer Nature B.V</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>7SS</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5918-1799</orcidid><orcidid>https://orcid.org/0000-0003-4448-5196</orcidid></search><sort><creationdate>2022</creationdate><title>Novel and stable QTL regions conferring resistance to MYMV disease and its inheritance in blackgram (Vignamungo (L.) Hepper)</title><author>Subramaniyan, Ragul ; Narayana, Manivannan ; Krishnamoorthy, Iyanar ; Natarajan, Ganapathy ; Gandhi, Karthikeyan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-d5859e404dd03af1e38f83aa8e9e56472d15ebda1d120ca7a45e71da7fdfb9033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animal Genetics and Genomics</topic><topic>Biomedical and Life Sciences</topic><topic>Disease resistance</topic><topic>Disease Resistance - genetics</topic><topic>Evolutionary Biology</topic><topic>Genotypes</topic><topic>Heredity</topic><topic>Life Sciences</topic><topic>Microbial Genetics and Genomics</topic><topic>Phenotyping</topic><topic>Plant Breeding</topic><topic>Plant Diseases - genetics</topic><topic>Plant Genetics and Genomics</topic><topic>Population studies</topic><topic>Quantitative Trait Loci</topic><topic>Research Article</topic><topic>Vigna - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Subramaniyan, Ragul</creatorcontrib><creatorcontrib>Narayana, Manivannan</creatorcontrib><creatorcontrib>Krishnamoorthy, Iyanar</creatorcontrib><creatorcontrib>Natarajan, Ganapathy</creatorcontrib><creatorcontrib>Gandhi, Karthikeyan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Subramaniyan, Ragul</au><au>Narayana, Manivannan</au><au>Krishnamoorthy, Iyanar</au><au>Natarajan, Ganapathy</au><au>Gandhi, Karthikeyan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel and stable QTL regions conferring resistance to MYMV disease and its inheritance in blackgram (Vignamungo (L.) Hepper)</atitle><jtitle>Journal of genetics</jtitle><stitle>J Genet</stitle><addtitle>J Genet</addtitle><date>2022</date><risdate>2022</risdate><volume>101</volume><issue>1</issue><artnum>18</artnum><issn>0022-1333</issn><eissn>0973-7731</eissn><abstract>Mungbean yellow mosaic virus (MYMV) disease is a significant constraint for blackgram production. The present study employed a mapping population derived from a cross between susceptible (MDU 1) and resistant (TU 68) genotypes to identify quantitative trait loci (QTL) associated with MYMV disease resistance in addition to bruchine resistance loci identified from the previous study. Phenotyping was carried out in F
2
generation under the disease spreader row method at field condition. Disease score observations were carried out 60 days after sowing (DAS). The chi-square goodness of fit test revealed inhibitory gene action with two genes controlling the expression of resistance to MYMV disease. However, QTL analysis revealed one major QTL region, i.e.
qMYMVD_60
at LG 10 responsible for MYMV disease score at 60 DAS, accounted for 21 per cent of variation. The identified QTL has the flanking markers as CEDG180 and CEDG116. Hence, the QTL,
qMYMVD_60
may be utilized in the breeding of MYMV disease resistance. Further, the marker-assisted introgression of both the MYMV and bruchine resistance QTLs can be performed in the near future.</abstract><cop>New Delhi</cop><pub>Springer India</pub><pmid>35221312</pmid><doi>10.1007/s12041-022-01359-w</doi><orcidid>https://orcid.org/0000-0001-5918-1799</orcidid><orcidid>https://orcid.org/0000-0003-4448-5196</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-1333 |
ispartof | Journal of genetics, 2022, Vol.101 (1), Article 18 |
issn | 0022-1333 0973-7731 |
language | eng |
recordid | cdi_proquest_miscellaneous_2634520055 |
source | MEDLINE; Indian Academy of Sciences; SpringerLink Journals; EZB-FREE-00999 freely available EZB journals |
subjects | Animal Genetics and Genomics Biomedical and Life Sciences Disease resistance Disease Resistance - genetics Evolutionary Biology Genotypes Heredity Life Sciences Microbial Genetics and Genomics Phenotyping Plant Breeding Plant Diseases - genetics Plant Genetics and Genomics Population studies Quantitative Trait Loci Research Article Vigna - genetics |
title | Novel and stable QTL regions conferring resistance to MYMV disease and its inheritance in blackgram (Vignamungo (L.) Hepper) |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T15%3A04%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Novel%20and%20stable%20QTL%20regions%20conferring%20resistance%20to%20MYMV%20disease%20and%20its%20inheritance%20in%20blackgram%20(Vignamungo%20(L.)%20Hepper)&rft.jtitle=Journal%20of%20genetics&rft.au=Subramaniyan,%20Ragul&rft.date=2022&rft.volume=101&rft.issue=1&rft.artnum=18&rft.issn=0022-1333&rft.eissn=0973-7731&rft_id=info:doi/10.1007/s12041-022-01359-w&rft_dat=%3Cproquest_cross%3E2633262120%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2633262120&rft_id=info:pmid/35221312&rfr_iscdi=true |