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Dive into the research topics where Todd A. Sangster is active.

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Featured researches published by Todd A. Sangster.


Nature | 2002

Hsp90 as a capacitor of phenotypic variation.

Christine Queitsch; Todd A. Sangster; Susan Lindquist

Heat-shock protein 90 (Hsp90) chaperones the maturation of many regulatory proteins and, in the fruitfly Drosophila melanogaster, buffers genetic variation in morphogenetic pathways. Levels and patterns of genetic variation differ greatly between obligatorily outbreeding species such as fruitflies and self-fertilizing species such as the plant Arabidopsis thaliana. Also, plant development is more plastic, being coupled to environmental cues. Here we report that, in Arabidopsis accessions and recombinant inbred lines, reducing Hsp90 function produces an array of morphological phenotypes, which are dependent on underlying genetic variation. The strength and breadth of Hsp90s effects on the buffering and release of genetic variation suggests it may have an impact on evolutionary processes. We also show that Hsp90 influences morphogenetic responses to environmental cues and buffers normal development from destabilizing effects of stochastic processes. Manipulating Hsp90s buffering capacity offers a tool for harnessing cryptic genetic variation and for elucidating the interplay between genotypes, environments and stochastic events in the determination of phenotype.


Proceedings of the National Academy of Sciences of the United States of America | 2008

HSP90 affects the expression of genetic variation and developmental stability in quantitative traits

Todd A. Sangster; Neeraj Salathia; Soledad F. Undurraga; Ron Milo; Kurt Schellenberg; Susan Lindquist; Christine Queitsch

Modulation of the activity of the molecular chaperone HSP90 has been extensively discussed as a means to alter phenotype in many traits and organisms. Such changes can be due to the exposure of cryptic genetic variation, which in some instances may also be accomplished by mild environmental alteration. Should such polymorphisms be widespread, natural selection may be more effective at producing phenotypic change in suboptimal environments. However, the frequency and identity of buffered polymorphisms in natural populations are unknown. Here, we employ quantitative genetic dissection of an Arabidopsis thaliana developmental response, hypocotyl elongation in the dark, to detail the underpinnings of genetic variation responsive to HSP90 modulation. We demonstrate that HSP90-dependent alleles occur in continuously distributed, environmentally responsive traits and are amenable to quantitative genetic mapping techniques. Furthermore, such alleles are frequent in natural populations and can have significant effects on natural phenotypic variation. We also find that HSP90 modulation has both general and allele-specific effects on developmental stability; that is, developmental stability is a phenotypic trait that can be affected by natural variation. However, effects of revealed variation on trait means outweigh effects of decreased developmental stability, and the HSP90-dependent trait alterations could be acted on by natural selection. Thus, HSP90 may centrally influence canalization, assimilation, and the rapid evolutionary alteration of phenotype through the concealment and exposure of cryptic genetic variation.


PLOS ONE | 2007

Phenotypic Diversity and Altered Environmental Plasticity in Arabidopsis thaliana with Reduced Hsp90 Levels

Todd A. Sangster; Adam K. Bahrami; Amity Wilczek; Etsuko Watanabe; Kurt Schellenberg; Catherine A. McLellan; Alicia Kelley; Sek Won Kong; Christine Queitsch; Susan Lindquist

The molecular chaperone HSP90 aids the maturation of a diverse but select set of metastable protein clients, many of which are key to a variety of signal transduction pathways. HSP90 function has been best investigated in animal and fungal systems, where inhibition of the chaperone has exceptionally diverse effects, ranging from reversing oncogenic transformation to preventing the acquisition of drug resistance. Inhibition of HSP90 in the model plant Arabidopsis thaliana uncovers novel morphologies dependent on normally cryptic genetic variation and increases stochastic variation inherent to developmental processes. The biochemical activity of HSP90 is strictly conserved between animals and plants. However, the substrates and pathways dependent on HSP90 in plants are poorly understood. Progress has been impeded by the necessity of reliance on light-sensitive HSP90 inhibitors due to redundancy in the A. thaliana HSP90 gene family. Here we present phenotypic and genome-wide expression analyses of A. thaliana with constitutively reduced HSP90 levels achieved by RNAi targeting. HSP90 reduction affects a variety of quantitative life-history traits, including flowering time and total seed set, increases morphological diversity, and decreases the developmental stability of repeated characters. Several morphologies are synergistically affected by HSP90 and growth temperature. Genome-wide expression analyses also suggest a central role for HSP90 in the genesis and maintenance of plastic responses. The expression results are substantiated by examination of the response of HSP90-reduced plants to attack by caterpillars of the generalist herbivore Trichoplusia ni. HSP90 reduction potentiates a more robust herbivore defense response. In sum, we propose that HSP90 exerts global effects on the environmental responsiveness of plants to many different stimuli. The comprehensive set of HSP90-reduced lines described here is a vital instrument to further examine the role of HSP90 as a central interface between organism, development, and environment.


Proceedings of the National Academy of Sciences of the United States of America | 2008

HSP90-buffered genetic variation is common in Arabidopsis thaliana

Todd A. Sangster; Neeraj Salathia; Hana N. Lee; Etsuko Watanabe; Kurt Schellenberg; Keith Morneau; Hui Wang; Soledad F. Undurraga; Christine Queitsch; Susan Lindquist

HSP90 is a protein chaperone particularly important in the maturation of a diverse set of proteins that regulate key steps in a multitude of biological processes. Alterations in HSP90 function produce altered phenotypes at low penetrance in natural populations. Previous work has shown that at least some of these phenotypes are due to genetic variation that remains phenotypically cryptic until it is revealed by the impairment of HSP90 function. Exposure of such “buffered” genetic polymorphisms can also be accomplished by environmental stress, linking the appearance of new phenotypes to defects in protein homeostasis. Should such polymorphisms be widespread, natural selection may be more effective at producing phenotypic change in suboptimal environments. In evaluating this hypothesis, a key unknown factor is the frequency with which HSP90-buffered polymorphisms occur in natural populations. Here, we present Arabidopsis thaliana populations suitable for genetic mapping that have constitutively reduced HSP90 levels. We employ quantitative genetic techniques to examine the HSP90-dependent polymorphisms affecting a host of plastic plant life-history traits. Our results demonstrate that HSP90-dependent natural variation is present at high frequencies in A. thaliana, with an expectation that at least one HSP90-dependent polymorphism will affect nearly every quantitative trait in progeny of two different wild lines. Hence, HSP90 is likely to occupy a central position in the translation of genotypic variation into phenotypic differences.


Cell Cycle | 2003

Hsp90 and chromatin: where is the link?

Todd A. Sangster; Christine Queitsch; Susan Lindquist

No abstract available.


BioEssays | 2004

Under cover: causes, effects and implications of Hsp90‐mediated genetic capacitance

Todd A. Sangster; Susan Lindquist; Christine Queitsch


Current Opinion in Plant Biology | 2005

The HSP90 chaperone complex, an emerging force in plant development and phenotypic plasticity

Todd A. Sangster; Christine Queitsch


Plant Journal | 2007

Indel arrays : an affordable alternative for genotyping

Neeraj Salathia; Hana N. Lee; Todd A. Sangster; Keith Morneau; Christian R. Landry; Kurt Schellenberg; Aditi S. Behere; Kevin L. Gunderson; Duccio Cavalieri; Georg Jander; Christine Queitsch


Plant Journal | 2007

TECHNICAL ADVANCE: Indel arrays: an affordable alternative for genotyping

Neeraj Salathia; Hana N. Lee; Todd A. Sangster; Keith Morneau; Christian R. Landry; Kurt Schellenberg; Aditi S. Behere; Kevin L. Gunderson; Duccio Cavalieri; Georg Jander; Christine Queitsch


Cell Cycle | 2003

Hsp90 and chromatin

Todd A. Sangster; Christine Queitsch; Susan Lindquist

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Susan Lindquist

Massachusetts Institute of Technology

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Aditi S. Behere

Boyce Thompson Institute for Plant Research

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Georg Jander

Boyce Thompson Institute for Plant Research

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