Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/1123
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dc.contributor.authorGautam, Vibhav-
dc.contributor.authorSingh, Archita-
dc.contributor.authorYadav, Sandeep-
dc.contributor.authorSingh, Sharmila-
dc.contributor.authorKumar, Pramod-
dc.contributor.authorDas, Shabari Sarkar-
dc.contributor.authorSarkar, Ananda K.-
dc.date.accessioned2020-11-12T05:48:48Z-
dc.date.available2020-11-12T05:48:48Z-
dc.date.issued2021-
dc.identifier.citationDevelopment, 148: dev190033en_US
dc.identifier.issn1477-9129-
dc.identifier.otherhttps://doi.org/10.1242/dev.190033-
dc.identifier.urihttps://dev.biologists.org/content/early/2020/11/08/dev.190033-
dc.identifier.urihttp://223.31.159.10:8080/jspui/handle/123456789/1123-
dc.descriptionAccepted date: November 2, 2020en_US
dc.description.abstractRoot system architecture and anatomy of monocotyledonous maize is significantly different from dicotyledonous model Arabidopsis. The molecular role of non-coding RNA (ncRNA) is poorly understood in maize root development. Here we address the role of LEAFBLADELESS1 (LBL1), a component of maize trans-acting short-interfering RNA (ta-siRNA), in maize root development. We report that the root growth, anatomical patterning, number of lateral roots (LRs) and monocot-specific crown roots (CRs) and seminal roots (SRs) are significantly affected in lbl1-rgd1 mutant, which is defective in production of ta-siRNA, including tasiR-ARF that targets AUXIN RESPONSE FACTOR3 (ARF3) in maize. Altered accumulation and distribution of auxin, due to differential expression of auxin biosynthesis and transporter genes, created an imbalance in auxin signaling. Altered expression of microRNA165/166 (miR165/166) and its targets ROLLED1/2 (RLD1/2) contributed to the changes in lbl1-rgd1 root growth and vascular patterning, as was evident by altered root phenotype of Rld1-O semi-dominant mutant. Thus, LBL1/ta-siRNA module regulates root development, possibly by affecting auxin distribution and signaling, in crosstalk with miR165/166-RLD1/2 module. We further showed that ZmLBL1 and its Arabidopsis homolog AtSGS3 proteins are functionally conserved.en_US
dc.description.sponsorshipVG, ArS, SS, PK thanks, Council of Scientific and Industrial Research (CSIR, Govt. of India), New Delhi India for fellowship. SY thanks University Grants Commission (UGC, India) and National Institute of Plant Genome Research, New Delhi (NIPGR) for fellowship. SSD acknowledges Vidyasagar University for support. AKS acknowledges NIPGR for funding and necessary infrastructural setups. We acknowledge the Central Instrument Facility (NIPGR, New Delhi) for real time PCR, microtome, and light/confocal microscopes, plant growth facility, and other facilities. We sincerely thank Prof. Marja Timmermans (CSHL, USA; currently, Univ. of Tubingen, Germany) for plant material support and valuable critical comments on the manuscript. We thank Prof. Klaus Palme for providing PIN1 antibody. We acknowledge the DBT‐eLibrary Consortium (DeLCON) for providing access to e‐resources. We also acknowledge ABRC, TAIR and Maize GDB for plant material/ genomic sequence resources.en_US
dc.language.isoen_USen_US
dc.publisherThe Company of Biologistsen_US
dc.subjectsmall RNAen_US
dc.subjectta-siRNAen_US
dc.subjectLBL1en_US
dc.subjectroot developmenten_US
dc.subjectvascular patterningen_US
dc.subjectmaizeen_US
dc.titleConserved LBL1-ta-siRNA and miR165/166-RLD1/2 modules regulate root development in maizeen_US
dc.typeArticleen_US
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