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Summary: An overview of cellular and epigenetic dynamics of human male germline development from germline specification to spermatogenesis, highlighting the conserved and divergent features between mice and humans.

STEM CELLS AND REGENERATION

Highlighted Article: Mouse gastruloids, 3D in vitro models of gastrulation, contain a population of primordial germ cell (PGC)-like cells that resemble early PGCs in vivo and are closely associated with neighbouring tissues during their development.

RESEARCH ARTICLES

Highlighted Article: Activated DAF-16, a FOXO transcription factor working downstream of the conserved insulin signaling pathway, senses DNA damage signals from the uterus to arrest oogenesis, thereby ensuring progeny fitness.

Summary: Chondroitin sulfate depletion results in muscle dysfunction and disrupted mechanical properties of the basement membrane, leading to age-dependent morphological defects in Drosophila.

Highlighted Article: Region-specific rotation of the planar cell polarity axis correlates with reversed hair follicle orientation in the rosette fancy mouse.

Summary: Using an oocyte-specific knockout, we demonstrate that UBE2I is required for timing key hallmarks of oocyte development, including chromatin organization, transcriptional regulation, meiotic progression and maintenance of fully-grown cell identity.

Highlighted Article: Optogenetic dissection of the incoherent feedforward loop regulating brachyenteron in the Drosophila embryo reveals that temporal dynamics and spatial diffusion contribute to stripe formation.

Summary: Notch-driven basal extrusion and Piezo1-mediated apical extrusion work in concert to ensure that all multiciliated cells are lost from the epithelium by stage 48 of Xenopus embryonic development.

Highlighted Article: Using transgenic mice that overexpress Sall1 in ovaries, we demonstrate the capacity of this factor to activate kidney-related gene programs that are also observed during mole ovotestis formation.

Highlighted Article: Cleavage-resistant EpCAM does not prevent intestinal failure in the Spint2-deficient mouse model of congenital tufting enteropathy, challenging the current model of proteolysis-driven disease progression.

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