Plants respond to abiotic stress through a variety of physiological, biochemical, and transcriptional mechanisms. Many genes exhibit altered levels of expression in response to abiotic stress, which requires concerted action of both
Despite myriad examples of local adaptation, the phenotypes and genetic variants underlying such adaptive differentiation are seldom known. Recent work on freezing tolerance and local adaptation in ecotypes of
We examined the consequences of a naturally occurring loss‐of‐function (
Freezing tolerance was lower in the Italian (11%) compared to the Swedish (72%) ecotype, and all four experimental
We identified 10 genes that are at least partially regulated by
- NSF-PAR ID:
- 10458095
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- American Journal of Botany
- Volume:
- 107
- Issue:
- 2
- ISSN:
- 0002-9122
- Page Range / eLocation ID:
- p. 250-261
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract Questions What are the primary biotic and abiotic factors driving composition and abundance of naturally regenerated tree seedlings across forest landscapes of Maine? Do seedling species richness (
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USA and Canada. Despite limitations associated with relatively small plot size, large seedling size class and lack of direct measurements of light, water and nutrients, this study documents the influence of these factors amid high variability associated with patterns of natural regeneration. The curvilinear relationship between mean annual temperature withSR andSD supports the argument that species richness and abundance usually have unimodal relationships with productivity indicators, whereas the curvilinear relationship between overstorey tree size diversity andSR andSD suggest that moderate overstorey diversity incorporates multiple species as well as higher seedling individuals. -
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Abstract Ecotypic variation in forage nutrient value of a dominant grassland species,
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Premise Light is critical in the ability of plants to accumulate chlorophyll. When exposed to far‐red (
FR ) light and then grown in white light in the absence of sucrose, wild‐type seedlings fail to green in a response known as theFR block of greening (BOG ). This response is controlled by phytochrome A through repression of protochlorophyllide reductase‐encoding (POR ) genes byFR light coupled with irreversible plastid damage. Sigma (SIG ) factors are nuclear‐encoded proteins that contribute to plant greening and plastid development through regulating gene transcription in chloroplasts and impacting retrograde signaling from the plastid to nucleus.SIG s are regulated by phytochromes, and the expression of someSIG factors is reduced in phytochrome mutant lines, includingphyA . Given the association of phyA with theFR BOG and its regulation ofSIG factors, we investigated the potential regulatory role ofSIG factors in theFR BOG response.Methods We examined
FR BOG responses insig mutants, phytochrome‐deficient lines, and mutant lines for several phy‐associated factors. We quantified chlorophyll levels and examined expression of keyBOG ‐associated genes.Results Among six
sig mutants, only thesig6 mutant significantly accumulated chlorophyll afterFR BOG treatment, similar to thephyA mutant.SIG 6 appears to control protochlorophyllide accumulation by contributing to the regulation of tetrapyrrole biosynthesis associated with glutamyl‐tRNA reductase (HEMA 1) function, select phytochrome‐interacting factor genes (PIF4 andPIF6 ), andPENTA1 , which regulatesPORA mRNA translation afterFR exposure.Conclusions Regulation of
SIG6 plays a significant role in plant responses toFR exposure during theBOG response.
