Clonal and population variation in jellyfish symmetry

Author(s):  
Lisa-ann Gershwin

While it is generally assumed that jellyfishes (Cnidaria: Scyphozoa) are stably tetramerous, variation in symmetry (i.e. unimerous to octamerous) can be observed in most populations at a rate of approximately 2%, but sometimes as high as 10%. This type of variation has been observed among clonemates during strobilation in five taxa, namely Aurelia aurita, A. labiata, Chrysaora fuscescens, Pelagia colorata, and Phacellophora camtschatica. It is currently unclear whether the symmetry variation is caused by genetic, environmental, or developmental factors, or some combination. Although hexamerous lineages were not bred successfully, lineages were raised with rates of variation higher than normal. Thus, there may be some genetic component to the variation. In one lineage observed over 4.5 months, the rate of non-tetramery declined substantially from an initial high of 88.9% to a final cumulative low of 29%. Apparently this lineage was able to stabilize tetramery over time, possibly indicating some self-correcting developmental mechanism. Furthermore, no difference was found in variation rates between stressed and unstressed polyps, indicating that environmental factors may not play an important role in symmetry determination in these animals. These results indicate stabilizing selection in controlling the expression of variable symmetry.

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Yisong Huang ◽  
Shaoyong Su ◽  
Harold Snieder ◽  
Frank Treiber ◽  
Gaston Kapuku ◽  
...  

AbstractIncreased arterial stiffness measured by pulse wave velocity (PWV) is an important parameter in the assessment of cardiovascular risk. Our previous longitudinal study has demonstrated that carotid-distal PWV showed reasonable stability throughout youth and young adulthood. This stability might be driven by genetic factors that are expressed consistently over time. We aimed to illustrate the relative contributions of genetic and environmental factors to the stability of carotid-distal PWV from youth to young adulthood. We also examined potential ethnic differences. For this purpose, carotid-distal PWV was measured twice in 497 European American (EA) and African American (AA) twins, with an average interval time of 3 years. Twin modelling on PWV showed that heritability decreased over time (62–35%), with the nonshared environmental influences becoming larger. There was no correlation between the nonshared environmental factors on PWV measured at visit 1 and visit 2, with the phenotypic tracking correlation (r = 0.32) completely explained by shared genetic factors over time. Novel genetic influences were identified accounting for a significant part of the variance (19%) at the second measurement occasion. There was no evidence for ethnic differences. In summary, novel genetic effects appear during development into young adulthood and account for a considerable part of the variation in PWV. Environmental influences become larger with age for PWV.


2020 ◽  
Author(s):  
Tatyana Dobreva ◽  
David Brown ◽  
Jong Hwee Park ◽  
Matt Thomson

AbstractAn individual’s immune system is driven by both genetic and environmental factors that vary over time. To better understand the temporal and inter-individual variability of gene expression within distinct immune cell types, we developed a platform that leverages multiplexed single-cell sequencing and out-of-clinic capillary blood extraction to enable simplified, cost-effective profiling of the human immune system across people and time at single-cell resolution. Using the platform, we detect widespread differences in cell type-specific gene expression between subjects that are stable over multiple days.SummaryIncreasing evidence implicates the immune system in an overwhelming number of diseases, and distinct cell types play specific roles in their pathogenesis.1,2 Studies of peripheral blood have uncovered a wealth of associations between gene expression, environmental factors, disease risk, and therapeutic efficacy.4 For example, in rheumatoid arthritis, multiple mechanistic paths have been found that lead to disease, and gene expression of specific immune cell types can be used as a predictor of therapeutic non-response.12 Furthermore, vaccines, drugs, and chemotherapy have been shown to yield different efficacy based on time of administration, and such findings have been linked to the time-dependence of gene expression in downstream pathways.21,22,23 However, human immune studies of gene expression between individuals and across time remain limited to a few cell types or time points per subject, constraining our understanding of how networks of heterogeneous cells making up each individual’s immune system respond to adverse events and change over time.


2019 ◽  
Vol 9 (6) ◽  
pp. 146 ◽  
Author(s):  
Sheerin ◽  
Kovalchick ◽  
Overstreet ◽  
Rappaport ◽  
Williamson ◽  
...  

: Genes, environmental factors, and their interplay affect posttrauma symptoms. Although environmental predictors of the longitudinal course of posttraumatic stress disorder (PTSD) symptoms are documented, there remains a need to incorporate genetic risk into these models, especially in youth who are underrepresented in genetic studies. In an epidemiologic sample tornado-exposed adolescents (n = 707, 51% female, Mage = 14.54 years), trajectories of PTSD symptoms were examined at baseline and at 4-months and 12-months following baseline. This study aimed to determine if rare genetic variation in genes previously found in the sample to be related to PTSD diagnosis at baseline (MPHOSPH9, LGALS13, SLC2A2), environmental factors (disaster severity, social support), or their interplay were associated with symptom trajectories. A series of mixed effects models were conducted. Symptoms decreased over the three time points. Elevated tornado severity was associated with elevated baseline symptoms. Elevated recreational support was associated with lower baseline symptoms and attenuated improvement over time. Greater LGLAS13 variants attenuated symptom improvement over time. An interaction between MPHOSPH9 variants and tornado severity was associated with elevated baseline symptoms, but not change over time. Findings suggest the importance of rare genetic variation and environmental factors on the longitudinal course of PTSD symptoms following natural disaster trauma exposure.


2020 ◽  
Vol 101 (3) ◽  
Author(s):  
Enrico Lunghi ◽  
Raoul Manenti ◽  
Fabio Cianferoni ◽  
Filippo Ceccolini ◽  
Michael Veith ◽  
...  

2006 ◽  
Vol 29 (4) ◽  
pp. 418-419 ◽  
Author(s):  
Joseph Polimeni

The only commonality between the various psychiatric disorders is that they reflect contemporary problematic behaviors. Some psychiatric disorders have a substantial genetic component, whereas others are essentially shaped by prevailing environmental factors. Because psychiatric ailments are so heterogeneous, any universal explanation of mental illness is not likely to have any clinical or theoretical utility.


2008 ◽  
Vol 11 (5) ◽  
pp. 531-537 ◽  
Author(s):  
Julie Aitken Schermer ◽  
N. T. Feather ◽  
Gu Zhu ◽  
Nicholas G. Martin

AbstractThe purpose of the present study was to examine the 10 value types from the Portrait Values Questionnaire (PVQ; Schwartz et al., 2001) both at the phenotypic (observed) level as well as the genetic and environmental level. Australian twins (N= 695) completed the PVQ as part of a larger questionnaire battery. Nine of the value types were found to have a genetic component with heritability estimates ranging from 10.8% for power to 38% for conformity. The achievement scale was best explained by environmental factors. The interscale correlations were found to range from –.02 to .70 at the phenotypic level. Of these 45 correlations, 16 were found to be explained by overlapping genetic factors and almost all (41) were found to have significant unique environment correlations.


Author(s):  
Daniel Ajzensztejn

The development of a cancer is often complex and multifactorial. Environmental factors such as smoking, diet, asbestos exposure, and sun exposure are important causes of cancer, with smoking alone responsible for 25%–30% of cancers. Up to 10% of cancers have a genetic component. Infectious agents are implicated in the development of approximately 15% of cancers. Viruses, bacteria, and parasites can all cause cancers. Cervical and hepatocellular carcinoma are the two commonest cancers related to infections.


1984 ◽  
Vol 33 (1) ◽  
pp. 130-143 ◽  
Author(s):  
Greta Robertson ◽  
Michael D. Lebowitz

2003 ◽  
Vol 93 (8) ◽  
pp. 1052-1055 ◽  
Author(s):  
Paul D. Manion

Foundation concepts in forest pathology are based on experiences evolving over time. Three examples will be addressed. (i) The primary concept behind education and research in forest pathology is the widely accepted attitude that disease-causing agents limit full utilization of forest resources. Therefore, we study diseases to find a weak link and then utilize this information to enhance our portion of the shared resource. The sustainable environmental issues of today have changed this concept, in my mind, to one of addressing what is the appropriate “healthy amount of disease” in a sustainable forest ecosystem. (ii) The initial concept that weakened understory trees and poorly managed forests deteriorate and decline over time because of numerous insults from biotic and abiotic agents has evolved into a decline disease stabilizing selection concept whereby healthy dominant trees in the forest (the survivors) are selectively killed by a combination of specifically ordered factors. (iii) The concept that heart-rot decay is initiated by infection through wounds that expose heartwood has evolved into the concept of infection in the sapwood that is compartmentalized over time in the center of the tree.


2020 ◽  
Author(s):  
Christopher Beam ◽  
Patrizia Pezzoli ◽  
Jane Mendle ◽  
S. Alexandra Burt ◽  
Michael C. Neale ◽  
...  

Conventional longitudinal behavioral genetic models estimate the relative contribution of genetic and environmental factors to stability and change of traits and behaviors. Longitudinal models rarely explain the processes that generate observed differences between genetically and socially related individuals. We propose that exchanges between people and their environments (i.e., phenotype-environment effects) can explain the emergence of observed differences over time. Such models, however, require violation of the independence assumption of standard behavioral genetic models, that is, uncorrelated genetic and environmental factors (Beam & Turkheimer, 2013; de Kort, Dolan, & Boomsma, 2012; Dolan, De Kort, Van Beijsterveldt, Bartels, & Boomsma, 2014). We review how specification of phenotype-environment effects contributes to understanding observed changes in genetic variability over time and longitudinal correlations among nonshared environmental factors. We then provide an example using 30 days of positive and negative affect scores from an all-female sample of twins. Results demonstrate that the phenotype-environment effects explain how heritability estimates fluctuate as well as how nonshared environmental factors persist over time. We discuss possible mechanisms underlying change in gene-environment correlation over time, the advantages and challenges of including gene-environment correlation in longitudinal twin models, and recommendations for future research.


Sign in / Sign up

Export Citation Format

Share Document