developmental symbiosis: integrating life histories through gene expression

1
Eco-Devo Workshop Program/Abstract # 47 The plasticity of sex Minoru Tanaka Laboratory of Molecular Genetics for Reproduction, National Institute for Basic Biology, Japan How sex is determined has been a topic of long standing broad interest. There are many types of sex determination system; genetic systems with different sex determination genes and environmental system with different critical temperatures. The subsequent process of sex differentiation following sex determination is not always straightforward. Some visual and neural system causes sex reversal during their life cycle and the endocrine system seems integrated in the mechanism of sex. These imply that some external and internal stimuli affect sex differentiation processes. Recent studies raise the possibility that these stimuli might cause unbalance between germ cells and somatic cells in some vertebrates. The balancing sex is conceptually important to understand establishment and mainte- nance of two different sexes, whose mechanism may be present behind many aspects of the phenotypic plasticity of sex. In this talk, I would like to raise open questions regarding the plasticity of sex and discuss about some possible mechanisms behind a variety of sex differentiation processes. doi:10.1016/j.ydbio.2010.05.079 Program/Abstract # 48 Developmental symbiosis: Integrating life histories through gene expression Scott F. Gilbert Dept. of Biology, Swarthmore College, Swarthmore, PA, USA Organisms do not develop autonomously. Rather, organisms have evolved to respond to signals from the outside environment. In many instances, these signals come from symbiotic organisms such as bacteria, fungi, algae, or protists. This appears to be the rulefor most species. In some instances, the symbiosis has become essential for the development of one of its partners, as in the wasp Asobara, where the Wolbachia bacteria are needed for the development of the female reproductive tract. Here, the bacteria are transmitted through the female germline in the same way as mitochondria. In other cases, symbionts are acquired by infection, as in the mammalian gut, which acquires bacteria from the mother. The gut bacteria induce specific gene expression in the intestinal cells, and they are needed for the formation of the villi capillaries and gut-associated lymphoid tissue. In some arthropods, infection by symbionts can change the sex of the carrier from male to female. These developmental associations are extremely important in medicine and conservation biology. Parasitic worms have been killed by antimicrobial drugs, and herbicides can prevent the development of salamanders by killing the algal symbionts needed by the eggs. We have outsourcedimportant developmental signals to symbionts, and this opens an entire new area for developmental biology. doi:10.1016/j.ydbio.2010.05.080 Program/Abstract # 49 Disruption of normal development with exogenous agents Kathleen K. Sulik Dept. of Cell and Dev. Biol., University of North Carolina, Chapel Hill, NC, USA The developmental basis of disease as it relates to prenatal exposure to endocrine-disrupting chemicals (EDCs) and to the teratogens, retinoic acid and alcohol, will be described. EDCs are a highly heterogeneous group of synthetic and natural chemicals that interfere with natural blood-borne hormones that are responsible for homeostasis, reproduction, and developmental processes. Among the synthetic EDCs are polychlorinated biphenyls (PCBs), dioxins, diethylstilbesterol (DES), and some plastics (e.g. bisphenol A), plasticizers (phthalates), pesticides, and fungicides. The phytoestro- gens, genistein and coumestrol, are examples of naturally-occurring EDCs. While a common target for many of these agents is the reproductive system, the mechanisms underlying EDC-induced disorders are diverse. Transgenerational effects have been reported and may result from overt mutation or epigenetic changes. The key to developmental/disease endpoints is the time in development when exposure to the causative exogenous agent occurs. In defining critical periods for induction of a wide range of abnormalities, including those of the urogenital tract, animal model systems have been employed. Notable in this regard are studies of retinoic acid and of alcohol-mediated teratogenesis following acute maternal exposure during narrow windows of development. The dysmorphogenesis that results from these teratogenic insults will be illustrated and critical periods for the induction of Retinoic Acid Embryopathy and Fetal Alcohol Spectrum Disorders in human populations will be discussed. Supported by NIH grants AA011605, AA017124, and AA019211. doi:10.1016/j.ydbio.2010.05.081 Contents lists available at ScienceDirect Developmental Biology journal homepage: www.elsevier.com/developmentalbiology Developmental Biology 344 (2010) 429

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Eco-Devo Workshop

Program/Abstract # 47The plasticity of sexMinoru TanakaLaboratory of Molecular Genetics for Reproduction,National Institute for Basic Biology, Japan

How sex is determined has been a topic of long standing broadinterest. There are many types of sex determination system; geneticsystems with different sex determination genes and environmentalsystem with different critical temperatures. The subsequent processof sex differentiation following sex determination is not alwaysstraightforward. Some visual and neural system causes sex reversalduring their life cycle and the endocrine system seems integrated inthe mechanism of sex. These imply that some external and internalstimuli affect sex differentiation processes. Recent studies raise thepossibility that these stimuli might cause unbalance between germcells and somatic cells in some vertebrates. The balancing sex isconceptually important to understand establishment and mainte-nance of two different sexes, whose mechanism may be presentbehind many aspects of the phenotypic plasticity of sex. In this talk, Iwould like to raise open questions regarding the plasticity of sex anddiscuss about some possible mechanisms behind a variety of sexdifferentiation processes.

doi:10.1016/j.ydbio.2010.05.079

Program/Abstract # 48Developmental symbiosis: Integrating life histories throughgene expressionScott F. GilbertDept. of Biology, Swarthmore College, Swarthmore, PA, USA

Organisms do not develop autonomously. Rather, organisms haveevolved to respond to signals from the outside environment. In manyinstances, these signals come from symbiotic organisms such asbacteria, fungi, algae, or protists. This appears to be the “rule” formost species. In some instances, the symbiosis has become essentialfor the development of one of its partners, as in the wasp Asobara,where the Wolbachia bacteria are needed for the development of thefemale reproductive tract. Here, the bacteria are transmitted throughthe female germline in the same way as mitochondria. In other cases,symbionts are acquired by infection, as in the mammalian gut, whichacquires bacteria from the mother. The gut bacteria induce specificgene expression in the intestinal cells, and they are needed for theformation of the villi capillaries and gut-associated lymphoid tissue.

In some arthropods, infection by symbionts can change the sex of thecarrier from male to female. These developmental associations areextremely important in medicine and conservation biology. Parasiticworms have been killed by antimicrobial drugs, and herbicides canprevent the development of salamanders by killing the algalsymbionts needed by the eggs. We have “outsourced” importantdevelopmental signals to symbionts, and this opens an entire newarea for developmental biology.

doi:10.1016/j.ydbio.2010.05.080

Program/Abstract # 49Disruption of normal development with exogenous agentsKathleen K. SulikDept. of Cell and Dev. Biol., University of North Carolina,Chapel Hill, NC, USA

The developmental basis of disease as it relates to prenatalexposure to endocrine-disrupting chemicals (EDCs) and to theteratogens, retinoic acid and alcohol, will be described. EDCs are ahighly heterogeneous group of synthetic and natural chemicals thatinterfere with natural blood-borne hormones that are responsible forhomeostasis, reproduction, and developmental processes. Among thesynthetic EDCs are polychlorinated biphenyls (PCBs), dioxins,diethylstilbesterol (DES), and some plastics (e.g. bisphenol A),plasticizers (phthalates), pesticides, and fungicides. The phytoestro-gens, genistein and coumestrol, are examples of naturally-occurringEDCs. While a common target for many of these agents is thereproductive system, the mechanisms underlying EDC-induceddisorders are diverse. Transgenerational effects have been reportedand may result from overt mutation or epigenetic changes. The key todevelopmental/disease endpoints is the time in development whenexposure to the causative exogenous agent occurs. In defining criticalperiods for induction of a wide range of abnormalities, includingthose of the urogenital tract, animal model systems have beenemployed. Notable in this regard are studies of retinoic acid and ofalcohol-mediated teratogenesis following acute maternal exposureduring narrow windows of development. The dysmorphogenesis thatresults from these teratogenic insults will be illustrated and criticalperiods for the induction of Retinoic Acid Embryopathy and FetalAlcohol Spectrum Disorders in human populations will be discussed.Supported by NIH grants AA011605, AA017124, and AA019211.

doi:10.1016/j.ydbio.2010.05.081

Contents lists available at ScienceDirect

Developmental Biology

j ourna l homepage: www.e lsev ie r.com/deve lopmenta lb io logy

Developmental Biology 344 (2010) 429