Braeckman BP et al. (2002) Aging Cell "Rebuttal to Van Voorhies: 'the influence of metabolic rate on longevity in the nematode Caenorhabditis elegans'."

Braeckman BP, Houthoofd K, Vanfleteren JR

[Aging Cell, 2002]

The papers by Van Voorhies in Free Radical Biology & Medicine (33, 587-596, 2002) and in this journal claim that the major longevity-extending mutations in C. elegans essentially act by reducing metabolic rate as predicted by the rate-of-living theory, and do not alter any metabolically independent mechanism specific to aging. In contrast, we found no evidence of a reduction in metabolic rate in these mutants using different experimental approaches. Now, Van Voorhies challenges the accuracy of our experimental results.

Sendinc E et al. (2015) Cell "Remodeling Your Way out of Cell Cycle."

Sendinc E, Shi Y, Jambhekar A

[Cell, 2015]

Throughout development, proliferative progenitors lose their mitotic potential, exit the cell cycle, and differentiate. In this issue, Ruijtenberg and van den Heuvel identify an important lineage-specific role for a SWI/SNF chromatin-remodeling complex that collaborates with core cell-cycle regulators to promote cell-cycle exit and terminal muscle cell differentiation.

Partridge L et al. (1992) Nature "Evolutionary biology. What the sperm count costs."

Partridge L, Harvey PH

[Nature, 1992]

Dissecting the sex life of the nematode worm Caenorhabditis elegans has already provided surprises for biologists interested in life-history theory. In a report on page 456 of this issue, Van Voorhies throws another spanner in the works by demonstrating that the costs of producing sperm are not as negligible as we might have thought.

Dehn AS et al. (2022) PLoS Biol "Binucleation ramps up gene expression meeting the physiological demands of an organism."

Dehn AS, Losick VP

[PLoS Biol, 2022]

In this issue of PLOS Biology, van Rijnberk and colleagues show how polyploidy, via binucleation, enables Caenorhabditis elegans intestinal cells to ramp up gene expression supplying the oocytes with the necessary lipids for optimal organismal growth and reproductive fitness.

Van Voorhies WA (2002) Aging Cell "Rebuttal to Braeckman et al: 'Assessing metabolic activity in again Caenorhabditis elegans: concepts and controversies'."

Van Voorhies WA

[Aging Cell, 2002]

The reviews by Braechman et al. and Van Voorhies in this issue of Aging Cell concur on the potential importance of metabolic rate and function to longevity in C. elegans. These reviews differ though, on their assessment of whether long-lived C. elegans mutants have a reduced metabolic rate compared to wild-type worms. At the centre of this disagreement are two main issues: the importance of measurement conditions when conducting metabolic assays on C. elegans, and which techniques are appropriate for measuring the metabolic rate of an organism and subsequent analysis of such data. These issues are interconnected; if the conditions under which an organism's metabolic rate are measured have a large impact on the resulting data, conclusions drawn from data collected from animals under different conditions may be invalid irrespective of the validity of the measurement methods. Conversely, measurement techniques which produce spurious data cannot be used to draw accurate conclusions about the metabolic rate of an organism, regardless of the conditions under which the organism was maintained.

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.

Kress E et al. (2011) Nat Cell Biol "Aurora A in cell division: kinase activity not required."

Kress E, Gotta M

[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.

Musacchio A (2015) Elife "Closing the Mad2 cycle."

Musacchio A

[Elife, 2015]

Chromosome separation is regulated by a cycle that involves a protein undergoing an unusual topological conversion.

Prosser SL et al. (2015) Curr Biol "Centrosome biology: the ins and outs of centrosome assembly."

Pelletier L, Prosser SL

[Curr Biol, 2015]

As a microtubule-organizing center, the centrosome undergoes a dramatic increase in size - via expansion of the pericentriolar material - during mitosis. Recent work reveals shared assembly properties of a protein scaffold that facilitates and supports this expansion, a process critical to spindle assembly.

Louis T et al. (2014) Cell "Neurons and behavior: ex uno, plures."

Louis T, Tomchik SM

[Cell, 2014]

Li et al. demonstrate that a single interneuron can regulate analog- and digital-like behaviors guided by two different postsynaptic neurons. Releasing a single neurotransmitter onto downstream neurons that express receptors with distinct biophysical properties enables a small set of neurons to direct a range of functional responses.