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[
Nature,
1999]
Advances in human genetics have meant that the genes mutated in human diseases can be identified exclusively by their location in the genome. But how do we work out the cellular functions of the associated protein products? Reports on pages 383 and 386 of this issue begin to address this problem for two proteins - polycystin-1 (PKD1) and polycystin-2 (PKD2) - that are defective in human kidney disease. From their studies of the nematode worm Caenorhabditis elegans, Barr and Sternberg present evidence that homologues of the polycystins act together in a signal-transduction pathway in sensory neurons. Chen et al., by contrast, have used an oocyte-expression system in the from Xenopus laevis to show that a homologue of PKD2 is associated with the activity of a cation channel. These results support the hypothesis that polycystin-related proteins belong to a hitherto unknown class of signal-transduction molecules.
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[
Nat Cell Biol,
2011]
Aurora A kinase is a key regulator of cell division, whose functions were attributed to its ability to phosphorylate diverse substrates. Aurora A is now shown to have a kinase-independent role in the regulation of chromatin-mediated microtubule assembly.
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[
Nature,
1998]
Some species of the nematode worm (Caenorhabditis elegans) are sociable diners, clumping together to share a meal, yet others are more solitary. Why? According to a report by de Bono and Bargmann, these differences can be explained by a change of just one amino acid in a putative neuropeptide receptor.
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Nat Neurosci,
2003]
In C. elegans, social and solitary feeding behavior can be determined by a single amino acid change in a G protein-coupled receptor. A new study identifies ligands for this receptor and suggests how changes in behavior evolve at the molecular level.
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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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[
Nature,
1992]
Induction is the process in development in which the fate of one cell mass is determined by another. A simple example occurs during vulval development in the nematode Caenorhabditis elegans: a gonadal cell called the anchor cell induces three neighbouring cells to embark on a programme of cell division and morphogenesis, which culminates, in a few hours, in the formation of a vulva. On page 470 of this issue, Hill and Sternberg report strong evidence that they have identified the anchor-cell signalling molecule, which they find is a member of the EGF (epidermal growth factor) group of growth factors.
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[
Nature,
2003]
Understanding how we grow old is a long-sought goal. A new large-scale study of gene expression in worms allows us to glimpse the complex biochemistry of lifespan.
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[
New York Times,
1992]
The simple act of making sperm substantially shortens a male worm's life span, a researcher has discovered in results that overturn accepted biological dogma about the relative cheapness of a male's ejaculation compared with the preciousness of a female's egg. The scientist studying simple but revealing worms called nematodes found that males live much shorter lives than their mates, and he has traced that discrepancy to sperm production.
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[
Nat Neurosci,
2000]
A recent Nature paper on mice lacking the Na+ channel BNC1 shows that this channel is essential for neuronal touch receptor function and may be part of a mechanosensory complex.
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[
Science,
1997]
A gene that helps control the life-span of the nematode C. elegans encodes the worm version of the insulin receptor, thereby providing a possible link between aging and glucose metabolism.