Plastids are organelles present in photosynthetic and nonphotosynthetic plant tissues. While it is well known that thioredoxin-dependent redox regulation is essential for leaf chloroplast function, little is known of the redox regulation in plastids of nonphotosynthetic tissues, which cannot use light as a direct source of reducing power. Thus, the question remains whether redox regulation operates in nonphotosynthetic plastid function and how it is integrated with chloroplasts for plant growth. Here, we show that NADPH-thioredoxin reductase C (NTRC), previously reported as exclusive to green tissues, is also expressed in nonphotosynthetic tissues of Arabidopsis thaliana, where it is localized to plastids. Moreover, we show that NTRC is involved in maintaining the redox homeostasis of plastids also in nonphotosynthetic organs. To test the relationship between plastids of photosynthetic and nonphotosynthetic tissues, transgenic plants were obtained with redox homeostasis restituted exclusively in leaves or in roots, through the expression of NTRC under the control of organ-specific promoters in the ntrc mutant. Our results show that fully functional root amyloplasts are not sufficient for root, or leaf, growth, but fully functional chloroplasts are necessary and sufficient to support wild-type rates of root growth and lateral root formation.
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http://dx.doi.org/10.1105/tpc.111.092304 | DOI Listing |
BMC Plant Biol
December 2024
College of Agronomy and Biotechnology, Key Laboratory for Crop Production and Smart Agriculture of Yunnan Province, Yunnan Agricultural University, Kunming, 650201, China.
Background: Yellow nutsedge (Cyperus esculentus, known as 'YouShaDou' in China, YSD) and purple nutsedge (Cyperus rotundus, known as 'XiangFuZi' in China, XFZ), closely related Cyperaceae species, exhibit significant differences in triacylglycerol (TAG) accumulation within their tubers, a key factor in carbon flux repartitioning that highly impact the total lipid, carbohydrate and protein metabolisms. Previous studies have attempted to elucidate the carbon anabolic discrepancies between these two species, however, a lack of comprehensive genome-wide annotation has hindered a detailed understanding of the underlying molecular mechanisms.
Results: This study utilizes transcriptomic analyses, supported by a comprehensive YSD reference genome, and metabolomic profiling to uncover the mechanisms underlying the major carbon perturbations between the developing tubers of YSD and XFZ germplasms harvested in Yunnan province, China, where the plant biodiveristy is renowned worldwide and may contain more genetic variations relative to their counterparts in other places.
Plant Physiol Biochem
November 2024
College of Agriculture, Guizhou University, Guiyang, 550025, China; Vegetable Research Academy, Guizhou University, Guiyang, 550025, China; Engineering Research Center for Protected Vegetable Crops in Higher Learning Institutions of Guizhou Province, Guiyang, 550025, China. Electronic address:
Tree Physiol
December 2024
Institute of Ecology and Earth Sciences, University of Tartu, J. Liivi 2, 50409 Tartu, Estonia.
Scenarios for future climate predict an increase in precipitation amounts and frequency of rain events, resulting in higher air humidity and soil moisture at high latitudes, including in northern Europe. We analysed the effects of artificially elevated environmental humidity (air relative humidity and soil moisture) on leaf gas exchange, water relations, growth and phenology of silver birch (Betula pendula) trees growing at the Free Air Humidity Manipulation (FAHM) experimental site situated in the hemiboreal vegetation zone, in eastern Estonia, with no occurring water deficit to the trees. The environmental humidity manipulation did not significantly affect the water relations traits but did affect some leaf gas exchange parameters, growth and phenology of the trees.
View Article and Find Full Text PDFFront Genet
November 2024
Centre for Advanced Studies on Climate Change, RPCAU, Samastipur, Bihar, India.
New Phytol
December 2024
School of Integrative Plant Science, Section of Plant Breeding and Genetics, Cornell University College of Agriculture and Life Sciences, Ithaca, NY, 14853, USA.
Carotenoids play essential roles in photosynthesis, photoprotection, and human health. Efforts to increase carotenoid content in several staple crops have been successful through both conventional selection and genetic engineering methods. Interestingly, in some cases, altering carotenoid content has had unexpected effects on other aspects of plant metabolism, impacting traits like sugar content, dry matter percentage, fatty acid content, stress tolerance, and phytohormone concentrations.
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