Search bioRxiv⌕ Search
Home/Archive/bioRxiv

bioRxiv · 10.1101/2022.01.26.477926

Sex-Specific Genes Identified in Sea Urchin Gonads are Expressed Prior to Metamorphosis

Pieplow, C.·Wessel, G. M.
View original source ↗Export metadata ↓

Abstract

A great collaboration between the germline and somatic cells of an organism is the creation of a functional gonad. Here we begin to test this mechanism in a sea urchin by use of RNA-seq, and quantitative mRNA measurements throughout the life cycle of the sea urchin, Lytechinus variegatus (Lv). We found through de novo analyses that the ovary and testis of this echinoderm contains the many transcripts predicted for gamete morphology and function, but we also discovered many uncharacterized gene products unique to each gonad. We found that transcripts involved in glycolysis are highly enriched in the ovary compared to the testis, and that Lv has an expansion of nanos genes not observed in other sequenced echinoderms. We developed a pipeline integrating timepoint RNA-seq data throughout development to identify hallmark gene expression in gonads. We found activation of meiotic genes surprisingly early in development, and observed that candidate genes involved in sex determination are first expressed during larval growth, well before metamorphosis. We further discovered that individual larvae express varying levels of male- or female-hallmark genes before metamorphosis, including factors for the germ line, oocyte, sperm, and meiosis related genes. Together these data support the hypothesis that sex determination in the sea urchin is initiated prior to metamorphosis, from a shared profile of male and female factors, and that the many uncharacterized genes unique to the gonads may reveal unique pathways and mechanisms in echinoderm reproduction. HighlightO_LITestis and Ovary of the sea urchin, Lytechinus variegatus, have distinct transcriptome profiles C_LIO_LIL. variegatus gonad RNA-seq reveals the expression of 9 nanos genes C_LIO_LIThe ovary in the sea urchin uniquely expresses genes of the glycolytic pathway, including an ovary-specific transcript of GAPDH C_LIO_LIGenes involved in meiosis and in sex determination are expressed early in larval development C_LIO_LIFrom gene expression profiles we conclude here that sex determination is initiated prior to metamorphosis in this echinoderm C_LI

Explore related subjects

developmental biologyPreprint

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Pieplow, C., Wessel, G. M.. 2022-01-28. Sex-Specific Genes Identified in Sea Urchin Gonads are Expressed Prior to Metamorphosis. https://doi.org/10.1101/2022.01.26.477926

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

bioRxiv2026

Neogenin-1 marks myeloid-primed fetal hematopoietic stem cells that undergo progressive lineage-restriction with age

During aging, hematopoietic stem cells (HSCs) increasingly shift from balanced to myeloid-biased differentiation, resulting in reduced lymphoid output and impaired adaptive immunity. The question of whether this lineage bias is established in a subset of HSCs during early development or primarily emerges with aging warrants further investigation. Here, we investigate whether myeloid-biased HSCs (my-HSCs) are established at the fetal liver stage by specifically examining Neogenin-1 (NEO1), a previously defined marker of my-HSCs. We identify two distinct populations of Hoxb5+ HSCs in the fetal liver: NEO1+ and NEO1-, with NEO1+ HSCs exhibiting transcriptional and functional characteristics consistent with my-HSCs. With age, my-HSC-associated transcriptional programs become increasingly reinforced across the Hoxb5+ pHSC compartment, with NEO1+ cells showing early enrichment of this program and both NEO1+ and NEO1- cells acquiring broader myeloid-biased features in aging. These findings suggest that lineage programming can begin early in development and is further shaped by age-related changes, potentially contributing to the functional decline observed in the aging hematopoietic system.

developmental biology↗
bioRxiv2026

Distinct roles for partially redundant transcription factors in Caenorhabditis elegans mesoderm lineage development

Developmental transcription factors often have overlapping functions, making it difficult to define the distinct roles of individual factors during lineage specification. We investigated the partially redundant transcription factors TBX-35 and CEH-51 in the Caenorhabditis elegans embryonic MS mesodermal lineage using 4D lineage tracing, reporter imaging, genetics, and single-cell RNA sequencing. In tbx-35 mutants, MS descendants showed progressively slower cell cycles and a division pattern that increasingly resembled the cousin C lineage. Fate-regulator expression also shifted toward C-like features, including ectopic pal-1 and expanded HLH-1 expression, although mutant cells did not simply adopt normal C-lineage positions. Loss of tbx-35 also impaired a later MS-dependent Notch induction in the AB lineage while leaving an earlier induction intact. CEH-51 showed a different pattern of activity whereby its protein became enriched in anterior MS daughters, and ceh-51 mutants produced later, more restricted lineage defects that were strongest in descendants of cells with higher CEH-51 levels. Single-cell profiling identified overlapping but nonidentical sets of genes dependent on the two factors. TBX-35-dependent changes were strongest at earlier stages, whereas CEH-51-dependent genes became more prominent later and were enriched in anterior MS sublineages. Finally, temperature-shift experiments determined that the severity and onset of tbx-35 mutant phenotypes depend on the maternal temperature environment and cannot be explained by differences in residual CEH-51 expression. These findings reveal that TBX-35 and CEH-51 contribute differently across the MS lineage and that reliable mesoderm development is supported by overlapping zygotic and maternal regulatory inputs.

developmental biology↗
bioRxiv2026

Dynamic microtubules drive yolk-cytoplasm segregation in the syncytial Drosophila embryo

Yolk-cytoplasm segregation is among the earliest spatial organization events in the developing embryo of many oviparous animals. The segregation process is intimately linked to early embryonic cleavage and pattern formation, and exhibits a wide range of spatial and temporal diversity. However, the underlying cytoskeletal mechanism remains largely unknown, except for a small number of species. Using quantitative live imaging, we investigated yolk segregation in the Drosophila embryo during the syncytial nuclear cycles 11-14. We find that the yolk vesicles move progressively inward in spatial and temporal coordination with the inward expanding microtubule networks that are nucleated from centrosomes positioned at the cortex, whereas cortical actin meshwork remains spatially restricted. Using the gnu RNAi embryo to decouple nuclear migration and division from cytoskeletal dynamics, we establish causality with targeted pharmacological disruption and find that microtubule dynamics is required for yolk segregation, while depolymerization of actin has no discernible effect. In support of a mechanism of growth-propelled passive displacement, microtubule plus end comets come in apparent contact with yolk vesicles, and injected, inert microbeads are displaced towards the embryo center presumably by the same pushing force. These findings identify microtubule polymerization as a predominant driver of yolk-cytoplasm segregation in Drosophila and suggest that diverse cytoskeletal mechanisms evolved to accomplish this crucial reorganization process

developmental biology↗