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[
Genome Biol,
2008]
: A report of the European C. elegans 2008 meeting, Seville, Spain, 29 March-2 April 2008.
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[
Invert Neurosci,
2013]
Some of the finest minds in the field of Caenorhabditis elegans neurobiology were brought together from 14 June to 17 June 2012 in the small, quaint and picturesque German city of Heidelberg for the biannual C. elegans neurobiology conference. Held at the EMBL Advanced Training Centre and wonderfully organised by Diah Yulianti, Jean-Louis Bessereau, Gert Jansen and William Schafer, the meeting contained 62 verbal presentations and hundreds of posters that were displayed around the double-helical walkways that looped throughout the conference centre. Presentations on recent advances in microfluidics, cell ablation and targeted gene expression exemplified the strengths of C. elegans as a model organism, with these advances allowing detailed high-throughput analysis and study. Interesting behaviours that were previously poorly characterised were widely discussed, as were the advantages of C. elegans as a model for neurodevelopment and neurodegeneration and the investigation of neuropeptide function. The examples discussed in this meeting report seek to illustrate the breadth and depth of presentations given on these recurring topics.
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[
Invert Neurosci,
2010]
Against the backdrop of the scenic Lake Mendota, the C. elegans Neurobiology Meeting came to a head. Expertly organised by Brian Ackley and Bruce Bamber and hosted at the accommodating University of Wisconsin, the meeting brought together recent contributions from many of the major research groups working on the neurobiology of C. elegans. With seven keynote speakers, 57 verbal presentations and hundreds of posters, this exciting event spanned a fascinating 3days from 27 June to 30 June 2010. In keeping with the tradition of this conference, the event on the whole was spearheaded by young investigators from several research institutions. The meeting served to emphasise the gains enjoyed by taking advantage of the genetic tractability of the worm. A thread that ran through the meeting was the importance of integrating data across different levels of biological organisation to permit delineation of the physiology underpinning discrete behavioural states. Recent advances in optogenetics and microfluidics were at the forefront of refining these analyses. The presentations discussed in this meeting report are a selection which reflects this overarching theme.
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[
Nat Genet,
2003]
In the year that the Nobel Prize was awarded to Sydney Brenner, Bob Horvitz and Sir John Suslton, the 14th International C. elegans meeting was bound to be a celebration as well as a scientific meeting and social get-together. The celebratory mood reached its high point during the keynote address by Sydney Brenner, the 'Father of the Worm'. The address was classic Brenner, at once provocative and Delphic, with incisive analogies, witty anecdotes and sweeping dismissals (systems biology did not fare well), all delivered with his usual flair.
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[
New Biol,
1991]
The biennial meeting on the nematode Caenorhabditis elegans, which has been held at Cold Spring Harbor on six previous occasions, this year grew too big for the motels of Long Island and moved westward to Madison, where over 500 participants spent 4 packed days discussing recent discoveries and future prospects. Gone are the days when research on this tiny worm seemed like a cottage industry, pursued only by a small group of devotees. However, the holistic approach to the nematode still prevails, as demonstrated by the absence of parallel sessions at the meeting. Genomics, genetics, neurobiology, cell biology, biochemistry, and development remain inextricably interwoven for most of the scientists studying C. elegans. Appropriately enough, biological interactions proved to be a leitmotiv of the 1991 meeting.
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[
J Gerontol A Biol Sci Med Sci,
2015]
In June 2013, a workshop was convened in San Francisco to explore, in depth, the role of the Forkhead transcription factor FOXO3 (and related FOXOs) in development, aging, and, in particular, exceptional longevity. The presentations covered results derived from model systems, computational analysis and bioinformatics, and genomics and genome-wide association studies of a number of cohorts. Although the data collectively strongly reinforce FOXO3 and the FOXO/FOXO3 pathway as very important determinants in aging and life span, much of the detail of how the latter is achieved still remains unknown, in part, because of the very large number of genes (~2,200 in Caenorhabditis elegans) the transcription factor is involved in helping regulate. Particularly challenging at the present time is understanding the association of apparently nonfunctional specific variants (single nucleotide polymorphisms) of FOXO3 and exceptional longevity in humans, a finding replicated in a number of studies. Nonetheless, as summarized in this report, valuable information and insights were presented at the workshop on the transcription factor including but not limited to its role in determining longevity in C elegans and Drosophila (in flies, eg, an important interaction in aging occurs between dFOXO and the transforming growth factor-/activin pathway), stem cell function and aging (notably in hematopoiesis), downstream regulatory activity (eg, by binding near sites of RNAse occupancy and altering chromatin structure), and as a potential target for the development a healthy aging drug (in this example, using compounds developed and screened to effect FOXO function in cancer cells).