Genome-Wide Identification of Medicago Peptides Involved in Macronutrient Responses and Nodulation1[OPEN]
Genome-wide annotation and RNA-seq analysis identify small secreted peptides responsive to nodulation and macronutrient limitations regulating root and nodule development in Medicago truncatula. Growing evidence indicates that small, secreted peptides (SSPs) play critical roles in legume growth and...
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Published in: | Plant physiology (Bethesda) Vol. 175; no. 4; pp. 1669 - 1689 |
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Main Authors: | , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
American Society of Plant Biologists
13-10-2017
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Online Access: | Get full text |
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Summary: | Genome-wide annotation and RNA-seq analysis identify small secreted peptides responsive to nodulation and macronutrient limitations regulating root and nodule development in Medicago truncatula.
Growing evidence indicates that small, secreted peptides (SSPs) play critical roles in legume growth and development, yet the annotation of SSP-coding genes is far from complete. Systematic reannotation of the
Medicago truncatula
genome identified 1,970 homologs of established SSP gene families and an additional 2,455 genes that are potentially novel SSPs, previously unreported in the literature. The expression patterns of known and putative SSP genes based on 144 RNA sequencing data sets covering various stages of macronutrient deficiencies and symbiotic interactions with rhizobia and mycorrhiza were investigated. Focusing on those known or suspected to act via receptor-mediated signaling, 240 nutrient-responsive and 365 nodulation-responsive Signaling-SSPs were identified, greatly expanding the number of SSP gene families potentially involved in acclimation to nutrient deficiencies and nodulation. Synthetic peptide applications were shown to alter root growth and nodulation phenotypes, revealing additional regulators of legume nutrient acquisition. Our results constitute a powerful resource enabling further investigations of specific SSP functions via peptide treatment and reverse genetics. |
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Bibliography: | T.C.d.B., P.K.L., X.D., R.D., P.X.Z., M.K.U., and W.-R.S. conceptualized the study and designed experiments; T.C.d.B., P.P., I.T.-J., V.V., and R.D performed plant growth experiments and collection of biological material; T.C.d.B., P.P., J.N., and I.T.-J. performed total RNA extractions; X.D., C.B., Z.Z., and P.X.Z. performed bioinformatic analyses; T.C.d.B. and P.K.L. performed RNA-seq data analysis and SSP and Focal List identifications; T.C.d.B., P.K.L., and S.R. performed synthetic peptide assays; P.K.L., T.C.d.B., C.B., P.X.Z., M.K.U., and W.-R.S. wrote the article. These authors contributed equally to the article. The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Wolf-Rüdiger Scheible (wrscheible@noble.org). Current address: Department of Biology, Eastern Connecticut State University, Willimantic, CT 06226. www.plantphysiol.org/cgi/doi/10.1104/pp.17.01096 |
ISSN: | 0032-0889 1532-2548 |
DOI: | 10.1104/pp.17.01096 |