Nectar biosynthesis is conserved among floral and extrafloral nectaries

Author:

Chatt Elizabeth C1ORCID,Mahalim Siti-Nabilla1ORCID,Mohd-Fadzil Nur-Aziatull1ORCID,Roy Rahul23ORCID,Klinkenberg Peter M2,Horner Harry T45ORCID,Hampton Marshall6ORCID,Carter Clay J2ORCID,Nikolau Basil J1ORCID

Affiliation:

1. Roy J. Carver Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, Ames, 50010, Iowa

2. Department of Plant and Microbial Biology, University of Minnesota Twin Cities, St. Paul, 55108, Minnesota

3. Department of Biology, St. Catherine University, St. Paul, 55105, Minnesota

4. Department of Genetics, Development and Cell Biology, Iowa State University, Ames, 50010, Iowa

5. Roy J. Carver High Resolution Microscopy Facility, Iowa State University, Ames, 50010, Iowa

6. Department of Mathematics and Statistics, University of Minnesota Duluth, Duluth, 55812, Minnesota

Abstract

Abstract Nectar is a primary reward mediating plant–animal mutualisms to improve plant fitness and reproductive success. Four distinct trichomatic nectaries develop in cotton (Gossypium hirsutum), one floral and three extrafloral, and the nectars they secrete serve different purposes. Floral nectar attracts bees for promoting pollination, while extrafloral nectar attracts predatory insects as a means of indirect protection from herbivores. Cotton therefore provides an ideal system for contrasting mechanisms of nectar production and nectar composition between different nectary types. Here, we report the transcriptome and ultrastructure of the four cotton nectary types throughout development and compare these with the metabolomes of secreted nectars. Integration of these datasets supports specialization among nectary types to fulfill their ecological niche, while conserving parallel coordination of the merocrine-based and eccrine-based models of nectar biosynthesis. Nectary ultrastructures indicate an abundance of rough endoplasmic reticulum positioned parallel to the cell walls and a profusion of vesicles fusing to the plasma membranes, supporting the merocrine model of nectar biosynthesis. The eccrine-based model of nectar biosynthesis is supported by global transcriptomics data, which indicate a progression from starch biosynthesis to starch degradation and sucrose biosynthesis and secretion. Moreover, our nectary global transcriptomics data provide evidence for novel metabolic processes supporting de novo biosynthesis of amino acids secreted in trace quantities in nectars. Collectively, these data demonstrate the conservation of nectar-producing models among trichomatic and extrafloral nectaries.

Funder

National Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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