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dc.contributor.authorBhogale, Snehaen_US
dc.contributor.authorMahajan, Ameya S.en_US
dc.contributor.authorNATARAJAN, BHAVANIen_US
dc.contributor.authorRajabhoj, Mohiten_US
dc.contributor.authorThulasiram, Hirekodathakallu V.en_US
dc.contributor.authorBANERJEE, ANJAN K.en_US
dc.date.accessioned2019-02-25T09:04:13Z
dc.date.available2019-02-25T09:04:13Z
dc.date.issued2014-02en_US
dc.identifier.citationPlant Physiology, 164(2), 1011-1027.en_US
dc.identifier.issn0032-0889en_US
dc.identifier.issn1532-2548en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2047-
dc.identifier.urihttps://doi.org/10.1104/pp.113.230714en_US
dc.description.abstractMicroRNA156 (miR156) functions in maintaining the juvenile phase in plants. However, the mobility of this microRNA has not been demonstrated. So far, only three microRNAs, miR399, miR395, and miR172, have been shown to be mobile. We demonstrate here that miR156 is a potential graft-transmissible signal that affects plant architecture and tuberization in potato (Solanum tuberosum). Under tuber-noninductive (long-day) conditions, miR156 shows higher abundance in leaves and stems, whereas an increase in abundance of miR156 has been observed in stolons under tuber-inductive (short-day) conditions, indicative of a photoperiodic control. Detection of miR156 in phloem cells of wild-type plants and mobility assays in heterografts suggest that miR156 is a graft-transmissible signal. This movement was correlated with changes in leaf morphology and longer trichomes in leaves. Overexpression of miR156 in potato caused a drastic phenotype resulting in altered plant architecture and reduced tuber yield. miR156 overexpression plants also exhibited altered levels of cytokinin and strigolactone along with increased levels of LONELY GUY1 and StCyclin D3.1 transcripts as compared with wild-type plants. RNA ligase-mediated rapid amplification of complementary DNA ends analysis validated SQUAMOSA PROMOTER BINDING-LIKE3 (StSPL3), StSPL6, StSPL9, StSPL13, and StLIGULELESS1 as targets of miR156. Gel-shift assays indicate the regulation of miR172 by miR156 through StSPL9. miR156-resistant SPL9 overexpression lines exhibited increased miR172 levels under a short-day photoperiod, supporting miR172 regulation via the miR156-SPL9 module. Overall, our results strongly suggest that miR156 is a phloem-mobile signal regulating potato development.en_US
dc.language.isoenen_US
dc.publisherAmerican Society of Plant Biologistsen_US
dc.subjectMicroRNA156en_US
dc.subjectGraft-Transmissible MicroRNAen_US
dc.subjectPlant Architectureen_US
dc.subjectTuberization in Solanum tuberosumen_US
dc.subjectAndigenaen_US
dc.subject2014en_US
dc.titleMicroRNA156: A Potential Graft-Transmissible MicroRNA That Modulates Plant Architecture and Tuberization in Solanum tuberosum ssp. Andigenaen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.identifier.sourcetitlePlant Physiologyen_US
dc.publication.originofpublisherForeignen_US
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