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Biology subjects

Scaramuzza, F.

Publications and source records attributed to Scaramuzza, F..

2 recordsLinked to original sources

Peripheral tissues of deep-sea mussels exhibit autonomous circadian timing via an atypical mechanism

While biological rhythms are crucial to life, the deep sea has long been considered an arrhythmic exception. However, at hydrothermal vents - devoid of diel cues yet shaped by tides - the mussel Bathymodiolus azoricus shows both tidal and, unexpectedly, circadian rhythms at -1700 m. Whether endogenous clock(s) drive these cycles remained unanswered. Here, we report endogenous circadian rhythms in B. azoricus cell cultures under constant conditions: isolated cells displayed a circadian oscillator despite tidal-dominant rhythms in situ. Reporter assays using genomic regions upstream of the mussels per gene and containing E-box motifs indicate that a functional transcription-translation feedback loop (TTFL) underpins circadian timing even in the deep sea. In contrast to conventional models, however, BazPeriod lacks autonomous repressive activity but modulates BazCry2. As BazPeriod itself oscillates tidally, it may explain how a single endogenous clock yields both tidal and diel rhythms. The work also spotlights the highly time-sensitive biology of vastly unexplored deep-sea biology.

molecular biology↗

A cryptochrome photoreceptor controls animal light-dependent growth and lifespan via evolutionary conserved hormonal pathways

Natural light is severely affected by human impact on Earth, yet little is known about the roles light receptors have outside vision and rhythmic processes. Here we show that loss-of-function of the light-receptive cryptochrome (l-cry) in marine bristleworms significantly increases lifespan and adult size, similarly to wild-types reared in constant darkness. Quantitative transcriptomics revealed hormonal players crucial for invertebrate and vertebrate sexual development and reproduction affected in l-cry mutants. These include nr0b1/2, ortholog of dax-1 (nr0b1) and shp (nr0b2), long considered vertebrate novelties. Depending on moon-phase, nr0b1/2 is up- or down-regulated in l-cry mutants. Matching the complex regulation, loss of nr0b1/2 function partially recapitulates l-cry phenotypes. Molecularly, Platynereis Nr0b1/2 affects steroidogenic and other endocrine pathways, nuclear receptor signaling, and transcription factor orthologs, involved in sexual developmental, reproductive, and timing processes in other organisms. Thus, our study reveals profound effects of light on adult animal life-time, likely at least in part by conserved endocrine pathways involved in sexual maturation and reproduction in annelids and vertebrates.

evolutionary biology↗