Steroid/thyroid hormone receptor genes in Caenorhabditis elegans.

The large family of steroid/thyroid hormone receptor (STR) genes has been extensively studied in vertebrates and insects but little information is available on it in more primitive organisms. All members possess a DNA binding domain of zinc fingers of the C2, C2 type. We have used the polymerase chain reaction with degenerate oligonucleotide primers covering this region to clone three distinct members of this family from the nematode Caenorhabditis elegans. All three belong to the retinoic acid receptor (RAR), thyroid hormone receptor subfamily of genes. The cDNA of one of these clones shows such a high homology to DHR3, an early ecdysone response gene found in Drosophila, and MHR3, identified in Manduca sexta, that we have termed it CHR3. Furthermore, the C-terminal portion of the deduced protein sequence shows a box containing eight identical amino acids among CHR3, DHR3, and MHR3 suggesting an identical specific ligand for these proteins. CNR8 shows homology to NAK1, and CNR14 has homology to both the RAR-gamma 1 gene and to another ecdysone response gene, E78A. Neither of the latter two cDNAs is a clear homologue of any known gene and each is distinctive. All of these genes are expressed varyingly in both larval and adult stages of nematode development as shown by Northern blot analyses. These data demonstrate that the STR family of genes is represented in a nematode whose ancestor appeared well before the branching that gave rise to the Arthropoda and Chordata.     

Hormonal regulation of aging and life span.

A regulatory growth factor pathway has been implicated in determination of longevity in a variety of species. Altered signaling in this pathway confers not only extended life spans but also increased resistance to oxidative stress. A new report using mice engineered to express fewer receptors for insulin-like growth factor (IGF-I), therefore reducing the signaling through this pathway, provides strong supporting evidence that IGF-I signaling does play a significant role in longevity. The IGF-I receptor knockdown mice were fertile, slightly smaller and resisted oxidative stressors more effectively when compared with normal littermate mice. This, along with other recent evidence, could provide clues towards potential therapeutic intervention to extend life span in humans.     

The neuroendocrine regulation of Drosophila aging

The rate of aging is regulated by hormones in insects and, most likely, in mammals. Mutations of the insulin-signaling pathway extend lifespan in the fruit fly and influence the level of other hormones, specifically juvenile hormone and the sterol ecdysone, each of which may directly influence senescence. With new genetic and genomic tools in Drosophila biology we are now exploring how the neuroendocrine system responds to environmental conditions to modify insulin action, how these signals control secondary hormones, and how these messages together modulate animal aging.     

Iron promotes protein insolubility and aging in C. elegans

Many late-onset proteotoxic diseases are accompanied by a disruption in homeostasis of metals (metallostasis) including iron, copper and zinc. Although aging is the most prominent risk factor for these disorders, the impact of aging on metallostasis and its role in proteotoxic disease remain poorly understood. Moreover, it is not clear whether a loss of metallostasis influences normal aging. We have investigated the role of metallostasis in longevity of Caenorhabditis elegans. We found that calcium, copper, iron, and manganese levels increase as a function of age, while potassium and phosphorus levels tend to decrease. Increased dietary iron significantly accelerated the age-related accumulation of insoluble protein, a molecular pathology of aging. Proteomic analysis revealed widespread effects of dietary iron in multiple organelles and tissues. Pharmacological interventions to block accumulation of specific metals attenuated many models of proteotoxicity and extended normal lifespan. Collectively, these results suggest that a loss of metallostasis with aging contributes to age-related protein aggregation.     

Endocrine regulation of aging and reproduction in Drosophila

Hormonal signals can modulate lifespan and reproductive capacity across the animal kingdom. The use of model organisms such as worms, flies and mice has been fundamentally important for aging research in the discovery of genetic alterations that can extend healthy lifespan. The effects of mutations in the insulin and insulin-like growth factor-like signaling (IIS) pathways are evolutionarily conserved in that they can increase lifespan in all three animal models. Additionally, steroids and other lipophilic signaling molecules modulate lifespan in diverse organisms. Here we shall review how major hormonal pathways in the fruit fly Drosophila melanogaster interact to influence reproductive capacity and aging.     

C. elegans,a model for aging with high-throughput capacity

The 1 mm long nematode Caenorhabditis elegans is one of the prime animal models to study the genetics of aging. Wild type animals under laboratory conditions live only for an average of 18 days, whereas mutations in about 50 genes have been identified that extend longevity up to sixfold. High-throughput analyses have been devised that allow large-scale analysis to identify additional genes, as well as compounds that affect life-span.     

An hypothesis concerning control networks and aging in Drosophila melanogaster and Caenorhabditis elegans

To explain trends emerging from the study of longevity mutants, a modification of the reactive oxygen species (ROS) model of aging is suggested. ROS do not appear to be produced in greater quantities during cellular activity unless specific factors are also present. These include raised cytosolic calcium and sodium ions, nitric oxide (NO) or dopamine. Metabolically active cells that are repeatedly exposed to these factors, especially in combination, show the most ROS damage and may contribute most to aging. This explains the importance of neurons, which is highlighted by genetic studies, and points to which cells are the most aging-sensitive. Control pathways disrupted in long-lived mutants are those which control one or more of these ROS promoting factors. The daf-2/daf-16 pathway may interact with these factors in several ways. Changes in control networks may be propagated from a relatively small number of cells/junctions by neural connectivity and hormonal means.     

Microarray analysis of variation in individual aging C. elegans: approaches and challenges

Aging is generally defined and studied as a population phenomenon. However, there is great interest, especially when discussing human aging, in the identification of factors that influence the life span of an individual organism. The nematode Caenorhabditis elegans provides an excellent model system for the study of aging at the level of the individual, since young nematodes are essentially clonal yet experience a large range of individual life spans. We are conducting gene expression profiling of individual nematodes, with the aim of discovering genes that vary stochastically in expression between individuals of the same age. Such genes are candidates to modulate the ultimate life span achieved by each individual. We here present statistical analysis of gene expression profiles of individual nematodes from two different microarray platforms, examining the issue of technical vs. biological variance as it pertains to uncovering genes of interest in this paradigm of individual aging.     

Steroid regulation of sexual behavior.

Investigation into the hormonal control of sexual behavior has a rich and extensive history. For many researchers currently active in the field, the physiological psychologist Frank A. Beach is recognized as the modern father of the study of hormones and behavior. His publication of the seminal book Hormones and Behavior-A Survey of Interrelationships Between Endocrine Secretions and Patterns of Overt Response, published in 1948, was a compilation of the previous 20 years of research establishing that gonadal secretions acted in the brain and modulated behavior. The question of precisely how hormones can alter brain functioning in a coordinated fashion and profoundly influence the patterns of behavioral responsiveness remains unanswered. As with many research areas, application of new techniques and approaches to the problem reveals additional layers of complexity and previously unimagined relationships between hormones, brain, and behavior. In addition, with the increasing understanding that the brain is a target organ for steroids, the implications of the ramifications of this steroid sensitivity have broadened. The hormonal regulation of sexual behavior is not an isolated aspect of steroid action in the brain; rather, it is one component of a host of physiological responses influenced by steroids. These include such diverse responses as anxiety, aggression, feeding, and learning and memory. An appreciation of the diverse effects of steroids has emerged from studies on sexual behavior, and a mutually beneficial relationship between this and other aspects of behavioral neuroscience has flourished and endured. As with all of neuroscience, this research area has been dynamic and progressive and has additionally benefited from a long history of comparative and integrative approaches to animal behavior.     

Control of Caenorhabditis elegans life history by nuclear receptor signal transduction

Caenorhabditis elegans diapause, reproductive development, and life span are influenced by the DAF-12 nuclear hormone receptor signaling pathway. Here, we describe how this nuclear receptor integrates environmental and physiologic cues and regulates developmental age, reproduction and aging.     

Paradoxical physiological transitions from aging to late life in Drosophila

In a variety of organisms, adulthood is divided into aging and late life, where aging is a period of exponentially increasing mortality rates and late life is a period of roughly plateaued mortality rates. In this study we used ～57,600 Drosophila melanogaster from six replicate populations to examine the physiological transitions from aging to late life in four functional characters that decline during aging: desiccation resistance, starvation resistance, time spent in motion, and negative geotaxis. Time spent in motion and desiccation resistance declined less quickly in late life compared to their patterns of decline during aging. Negative geotaxis declined at a faster rate in late life compared to its rate of decline during aging. These results yield two key findings: (1) Late-life physiology is distinct from the physiology of aging, in that there is not simply a continuation of the physiological trends which characterize aging; and (2) late life physiology is complex, in that physiological characters vary with respect to their stabilization, deceleration, or acceleration in the transition from aging to late life. These findings imply that a correct understanding of adulthood requires identifying and appropriately characterizing physiology during properly delimited late-life periods as well as aging periods.     

Genetics of aging in Drosophila.

The genetics of aging in Drosophila are reviewed under the separate headings of population genetics, physiological genetics, and molecular genetics. However, connections between these sub-fields are brought forward for discussion.     

Steroid priming of the luteinizing hormone response to luteinizing hormone releasing hormone.

Perifusion experiments were performed to study the stimulatory effects of luteinizing hormone releasing hormone (LH-RH) on the release of LH from anterior pituitary tissue. Exposure of pituitary tissue from normal male rats to LH-RH (5 ng/ml for 5 min) induced a small release of LH; in tissue from ovariectomized rats receiving no pretreatment, the release was more than three times greater and in tissue from gonadectomized male or female rats pretreated with oestradiol benzoate and progesterone, the release was six times greater than that observed in normal rats. Further exposure of pituitary tissue from gonadectomized steroid-pretreated male and female rats to LH-RH (5 ng/ml) induced an increase in the level of LH even greater than that seen after the initial exposure (priming action of LH-RH); in tissue from ovariectomized rats receiving no pretreatment, less LH was released than after the first exposure to LH-RH and in tissue from normal male rats the response was unchanged.