Kristin E. Gribble

Kristin E. Gribble
Assistant Scientist
e: kgribble@mbl.edu
p: 508 289 7194
f: 508 457 4727
Gribble CV

Dr. Gribble is a molecular biologist broadly interested in the evolution, ecology and life history of marine and freshwater plankton. She combines her training in biological oceanography, evolution, and molecular biology to investigate how environment and genetics influence the phenotypic plasticity of life history strategy and morphology to allow adaptation to changes in environmental conditions and to determine evolutionary fitness. By understanding the outcomes induced by specific environmental conditions, the molecular genetic bases of phenotypic changes, and the evolutionary conservation of plasticity, Dr. Gribble’s research enables predictions about the results of changing environmental conditions at scales ranging from the individual to the ecosystem.

Current Projects

Biology of Aging: Mechanisms and evolutionary conservation of therapeutic interventions

Therapies to improve health and increase lifespan rely on plasticity in life history. Limiting food intake, also known as caloric restriction (CR), is one of the most reliable means of extending lifespan in a variety of animals, yet the evolutionary origins and genetic mechanisms behind the response to CR are poorly understood. To determine the degree of conservation of responses to beneficial therapies, we investigated lifespan and fecundity changes in response to a variety of levels of CR among 12 strains of the rotifer Brachionus plicatilis isolated from different environments. The level of lifespan extension was different between sexual and asexual individuals of the same species. Interestingly, the degree of lifespan extension under CR was inversely correlated with lifespan under food-replete conditions. Differences in reproduction under varied CR regimens, even when lifespan extension was similar, suggested that different types of CR extend lifespan through diverse genetic mechanisms. Ongoing projects include analysis of differential gene expression over the rotifer life cycle and comparing gene expression in isolates with different responses to caloric restriction to identify genes involved in lifespan extension, using RNA-Seq. Additionally, we are testing the conservation of other lifespan-extending interventions, including the genetically-mediated response to low temperature.
Protoperidinium steidingerae isolated from the Atlantic Ocean, south of Martha’s Vineyard. Protoperidinium are single cell, heterotrophic dinoflagellates with complex life cycles; they occupy a unique position in the trophic dynamics of the plankton in marine systems, as they consume phytoplankton larger than themselves. Photo credit: Kristin Gribble.
Brachionus manjavacas female carrying a single egg. Brachionus rotifers are approximately 500 µm long, are composed of 1000 cells, and have defined digestive, nervous, reproductive and muscular systems. Monognont rotifers like Brachionus generally reproduce asexually, with occasional bouts of sexual reproduction. They play a significant role in freshwater and marine ecosystems as consumers of phytoplankton and bacteria and are emerging as an important model system for studying questions of evolution and the biology of aging. Photo credit: Kristin Gribble.

Biology of Aging: Maternal effects

Phenotypic plasticity may occur not only in an individual, but also across generations. Transgenerational phenotypic plasticity, known as a “maternal effects,” occurs when the maternal response to the environment causes a change in offspring phenotype without a change in the genome. While many studies have focused on the detrimental effects on progeny of advanced maternal age and harmful prenatal environments, little is known about the role of beneficial maternal inheritance on aging. The Gribble lab investigates the effects of maternal age and maternal CR on the lifespan and healthspan of Brachionus manjavacas offspring. With increasing maternal age, lifespan, health, and fecundity of female offspring decreases significantly. Interestingly, maternal CR partially rescues these effects, increasing the mean lifespan and fecundity of female offspring, even when those offspring are not directly exposed to CR. These findings point to the exciting possibility that beneficial maternal environments may have a positive effect on offspring aging, perhaps over multiple generations. We are investigating not only changes in phenotype and gene expression, but also the epigenetic changes associated with maternal age and maternal CR, and how these may transgenerationally alter gene expression in metabolic and repair pathways, leading to changes in offspring lifespan and healthspan. Epigenetic modifications—changes to DNA that regulate the activity of specific genes but not the underlying nucleotide sequence—play an active role in aging and are a likely mechanism for the transmission of maternal effects to offspring. Epigenetic mechanisms that regulate chromatin structure include DNA methylation and histone modifications such as methylation, acetylation, ubiquitination, phosphorylation, ADPribosylation, and sumoylation. The time scale of epigenetic histone modification allows phenotypic plasticity within a 1–3 generation window, and is thought to have evolved to deal with frequent environmental change, such as food level fluctuations, periodic hypoxia, and temperature shifts. Parental nutrition and stress impact the epigenetic profiles of subsequent generations and influence offspring metabolism, immune function, mental health, and behavior in humans and mammal model systems. Understanding the influence and mechanisms of maternal effects on aging will provide fertile ground for future research and for development of therapies to improve human health during aging.

Biological Oceanography

Previously, Dr. Gribble studied the ecology, molecular phylogeny, and life history of marine dinoflagellates (single cell aquatic protists), including harmful algal bloom phytoplankton and heterotrophic dinoflagellates. She described the relationship between the molecular phylogeny and morphological taxonomy of an important and widespread genus of heterotrophic dinoflagellates, Protoperidinium, and described the group’s biogeography off the western coast of Ireland. Dr. Gribble provided the first description of the life history, including sexual and asexual reproduction, of two species of Protoperidinium. The lab looks forward to continuing work on environmental regulators of life history strategy in marine phytoplankton in the future.

Current Lab Members

Erin Berry
Research Assistant II
e: eberry@mbl.edu
p: 508 289 7177
f: 508 457 4727

Emily Corey
Research Assistant I
e: gjarvis@mbl.edu
p: 508 289 7884
f: 508 457 4727

Opportunities in the Lab

Please contact Dr. Gribble about opportunities for postdocs, graduate students, research assistants, and interns in the laboratory.