Po MD et al. (2012) Neuron "Releasing the inner inhibition for axon regeneration."

Po MD, Calarco JA, Zhen M

[Neuron, 2012]

The adult mammalian central nervous system exhibits restricted regenerative potential. Chen etal. (2011) and El Bejjani and Hammarlund (2012) used Caenorhabditis elegans to uncover intrinsic factors that inhibit regeneration of axotomized mature neurons, opening avenues for potential therapeutics.

Akin O et al. (2014) Cell "The shape of things to come."

Akin O, Zipursky SL

[Cell, 2014]

Surface receptors can link binding of ligands to changes in the actin-based cell cytoskeleton. Chia etal. and Chen etal. provide evidence for direct binding between the cytoplasmic tails ofreceptorsand the WAVE complex, a regulator of the actin nucleator Arp2/3 complex, which mighthelp to explain how environmental signals are translated into changes in morphology andmotility.

Skourti-Stathaki K et al. (2013) Mol Cell "Histone 3 s10 phosphorylation: "caught in the R loop!"."

Skourti-Stathaki K, Proudfoot NJ

[Mol Cell, 2013]

In this issue of Molecular Cell, Castellano-Pozo etal. (2013) describe a connection between R loop structures and histone 3 S10 phosphorylation (H3S10P), a mark of chromatin compaction. Their results constitute asignificant advance in our understanding of the role of R loops in genomic instability.

Kumsta C et al. (2019) J Cell Biol "Getting under the skin: Cuticle damage elicits systemic autophagy response in C. elegans."

Hansen M, Kumsta C

[J Cell Biol, 2019]

In this issue, Zhang et al. (2019. <i>J. Cell. Biol.</i> https://doi.org/10.1083/jcb.201907196) describe a molecular mechanism by which cuticular damage in the nematode <i>C. elegans</i> leads to systemic induction of autophagy by signals propagated from sensory neurons via the TGF- signaling pathway.

Hickson GRX (2022) J Cell Biol "A back-up source of microtubules for the midbody during cytokinesis."

Hickson GRX

[J Cell Biol, 2022]

During cytokinesis, microtubules become compacted into a dense midbody prior to abscission. Using genetic perturbations and imaging of C. elegans zygotes, Hirsch et al. (2022. J. Cell Biol.https://doi.org/10.1083/jcb.202011085) uncover an unexpected source of microtubules that can populate the midbody when central spindle microtubules are missing.

Emmons SW et al. (1999) Nature "Signal transduction. Mating, channels and kidney cysts."

Somlo S, Emmons SW

[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.

Ma L et al. (2020) J Cell Biol "Membrane fusion drives pronuclear meeting in the one-cell embryo."

Starr DA, Ma L

[J Cell Biol, 2020]

The mechanisms that control how the two parental pronuclei fuse in the first mitosis of the embryo are poorly understood. In this issue, Rahman et al. (2020. J. Cell Biol.https://doi.org/10.1083/jcb.201909137) found that membrane fusion between pronuclear envelopes, followed by fenestration, promotes pronuclear fusion.

Little P (1992) Nature "DNA sequencing. The worm turns and delivers."

Little P

[Nature, 1992]

Supporters of large DNA sequencing projects will take heart (and find much to learn) from the report by J. Sulston and colleagues that appears on page 37 of this issue. Sulston et al. describe the first results of the Caenorhabditis elegans genome sequencing project, and have come up with not only hitherto unknown genes but also with fresh and biologically relevant information.

Garrity PA (2007) J Neurophysiol "Role of adaptation in C. elegans thermotaxis. Focus on "Short-term adaptation and temporal processing in the cryophilic response of Caenorabditis elegans"."

Garrity PA

[J Neurophysiol, 2007]

The work of Clark et al. in this issue of J. Neurophysiology extends the analysis of thermotaxis in C. elegans by providing a detailed analysis of the adaptation of thermotactic behavior. Previous work indicates that thermotaxis in C. elegans involves a biased random walk in which changes in temperature alter the duration of the runs that an animal makes between turns. Interestingly, the authors find that although behavioral responses to increases and decreases in temperature have opposite effects on run length, the two responses are of similar magnitude and adapt with similar kinetics. These properties are predicted to allow the system act as a band-pass filter that would be less sensitive to temperature fluctuations occurring on a time-scale significantly faster or slower than the time needed for an average run. This analysis of C. elegans thermotaxis raises potential parallels to bacterial chemotaxis, with the kinetics of adaptation playing an important role in determining the ability of the organism to sense a stimulus gradient. This raises the possibility that diverse organisms may exploit similar system properties to solve similar problems, such as the problem of responding robustly to subtle gradations in an external stimulus.

Tuck S (2011) Curr Biol "Extracellular vesicles: budding regulated by a phosphatidylethanolamine translocase."

Tuck S

[Curr Biol, 2011]

Recent work on a Caenorhabditis elegans transmembrane ATPase reveals a central role for the aminophospholipid phosphatidylethanolamine in the production of a class of extracellular vesicles.