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[
Dev Cell,
2012]
Chromatin diminution during development generates cells with varying genetic content within the same organism. Two recent papers demonstrate that in two different systems chromatin diminution removes a considerable number of genes from somatic cells, thereby restricting their expression to the germline.
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[
Cell,
2009]
The memory of somatic cell gene expression is reset in the germline in a process that is accompanied by dramatic changes in chromatin modifications. In this issue, Katz et al. (2009) show that the histone demethylase Lsd1/Spr-5 may participate in this resetting process in the worm, thereby preventing a decline in germ cell epigenetic stability and viability over ensuing generations.
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[
Cell Res,
2014]
In a recent paper in Nature, Ermolaeva et al. uncover a systemic response to DNA damage in germ cells that protects somatic tissues, providing mechanistic insight into the bidirectional communication between germ line and soma.
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[
Curr Biol,
2006]
Major sperm protein, a cytoskeletal molecule required for the amoeboid motility of sperm in Caenorhabditis elegans, also functions as a signaling molecule that regulates the rates of meiotic maturation and ovulation. Recent work has begun to uncover new genes required for the response to this signal in both somatic and germ line cells.
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[
Nat Cell Biol,
2004]
Why are proteins glycosylated? On the basis of new studies, I propose two models to clarify the specific functions of glycosylation in worms. The first explains how intra- and inter-cellular trafficking of an N-glycosylated disintegrin-metalloprotease guides somatic gonadal cells through their migratory route, determining the shape of an organ. The second explains how rigid coats of secreted chondroitin proteoglycans bend membranes to drive cytokinesis and epithelial invagination.
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[
Dev Cell,
2019]
Resource reallocation to metabolic processes promoting reproduction is critical for the survival of a species and therefore is tightly regulated. In this issue of Developmental Cell, Dowen (2019) finds that a PBX/MEIS homeodomain transcription factor complex controls a transcriptional network that balances reproduction versus longevity and somatic maintenance.
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[
Curr Biol,
2016]
Male nematodes secrete pheromones that accelerate the somatic senescence of potential mates. A new study shows that this harm most likely is an unintended by-product of the males' aim to speed up sexual maturation and delay reproductive senescence of future partners.
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[
Nat Cell Biol,
2010]
Recognition of apoptotic cells by phagocytic cells in Caenorhabditis elegans has been something of a mystery. A secreted transthyretin-like protein, TTR-52, has been identified as a bridging molecule between apoptotic cells and CED-1 on the phagocytic cells that engulf them.
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[
Dev Cell,
2019]
Bacterial avoidance and innate immune response are two ways by which C.elegans respond to pathogenic bacteria. In this issue of Developmental Cell, Kumar etal. (2019) and Singh and Aballay (2019) demonstrate that bacterial colonization is essential to induce both responses, which may be associated with somatic and reproductive longevity.
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[
Nature,
1999]
Animal evolution is commonly viewed as producing diverse, environmentally adapted bodies to propagate the germ line. The evolutionary theory of ageing suggests that genetic limits to lifespan may be inadvertent consequences of evolutionary selection for maximizing that propagation. In other words, trade-offs occur that favour reproductive success over post-reproductive longevity; lifespan should be inversely correlated with fecundity when progeny production diverts resources from the maintenance of somatic (non-reproductive) cells. The germ line contains all the genetic information to specify the soma. But it is also possible that there are other, environmentally modulated instructions for life history that the germ line conveys to the soma to maximize reproduction.