bioRxiv Science⌕ Search

bioRxiv · 10.64898/2025.12.30.697136

Tissue-specificity of gene expression in the Ciona embryo is subtly bimodal

Abstract

Expressed genes potentially fall into two distinct categories: tissue-specific genes expressed in a subset of cell types that carry out the distinctive functions of those cells; and housekeeping genes that are broadly expressed across all cell types and carry out the basic functions of life. It is unclear, however, whether these are actually two distinct classes or whether they represent an intuitive but false dichotomy imposed upon gene expression patterns that vary widely and continuously in how specific they are to particular tissues. We address this question using a high-coverage, whole-embryo single cell RNAseq atlas of the model invertebrate chordate Ciona robusta. There is a major complication in that quantitative measures of tissue-specificity such as the Tau and Gini metrics show a strong negative correlation with expression level. We show here that this correlation is the result of sampling error and not a fundamental biological relationship. Raw Tau scores are bimodal, but this is largely an artifact of Taus sigmoidal relationship with expression level for uniformly expressed genes. Simulations and statistical analyses indicate that the Tau metric is badly confounded by expression level for ubiquitously and/or weakly expressed genes but is relatively accurate for genes that have statistical evidence of differential expression. The distribution of tissue-specificity scores for these differentially expressed genes is broad and flat, spanning from near-binary to near-uniform. While only subtly bimodal, ubiquitously expressed and tissue-specific genes are clearly distinguishable, especially at higher expression levels. We explore the use of pseudocounts to shrink the high tissue-specificity scores of weakly expressed genes and find that they are effective at separating tissue-specific from ubiquitously expressed genes but distort rankings of tissue-specificity. Gene ontology code analysis indicates that the most tissue-specific genes are strongly enriched for predicted roles as transcriptional regulators and tissue-specific effector molecules, whereas the most ubiquitously expressed genes are enriched for predicted housekeeping functions. We conclude that the tissue-specific vs housekeeping dichotomy is meaningful in the Ciona embryo despite the broad range of Tau scores for tissue-specific genes. These findings provide a framework for formally assessing the tissue-specificity of gene expression across a broad range of taxa and developmental stages.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Veeman, M. T., Palmgren, K. R., Haas, C. L.. 2025-12-31. Tissue-specificity of gene expression in the Ciona embryo is subtly bimodal. https://doi.org/10.64898/2025.12.30.697136

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

KEEP EXPLORING

Related preprints

Integrative Nanopore and Illumina sequencing reveals age-associated tRNA modification and CCA-tail dynamics in yeast

Aging is characterized by a progressive loss of proteostasis. Transfer RNAs (tRNAs) are essential regulators of translation, yet their dynamics during aging remain poorly understood due to challenges in sequencing highly modified RNAs. Here we present a benchmarked Nanopore direct RNA sequencing (RNA004 chemistry) resource that profiles the Saccharomyces cerevisiae tRNAome during replicative aging at single-molecule resolution. Using in vitro transcribed tRNA controls, we establish modification detection thresholds and validate key findings with orthogonal Illumina sequencing. While overall tRNA abundance remains largely stable, our resource reveals age-associated terminal A cleavage at the 3' CCA tail of mature tRNAs, targeted T-loop and anticodon modification changes, and single-molecule evidence of modification co-occurrence. This dataset provides a resource for exploring tRNA regulation, translation fidelity, and longevity.

genomics↗

A hydrogen-producing mitochondrion in an anaerobic eukaryotrophic rhizarian

Diverse eukaryotes thrive under low oxygen conditions, in part through highly modified mitochondrion-related organelles (MROs) that use alternate metabolic pathways to support ATP production and cofactor recycling. Anaerobic lifestyles have evolved repeatedly across the eukaryotic tree of life, each providing an independent opportunity to understand how eukaryotes adapt to life in low oxygen conditions. Here, we use single-cell transcriptomics to reconstruct the MRO metabolism of PCE SSF, a benthic eukaryotrophic flagellate and the first cultivated representative of Novel Clade 12 (NC12; Rhizaria), an independently anaerobic rhizarian lineage. PCE SSF possesses an anaerobic hydrogen-producing mitochondrion capable of hydrogenosome-type substrate-level phosphorylation. It also retains a nearly complete but likely branched tricarboxylic acid pathway that lacks citrate synthase and malate dehydrogenase. The function of citrate synthase may instead be fulfilled by the typically cytosolic ATP citrate lyase, previously reported in this context only in the anaerobic cercozoan, Brevimastigomonas motovehiculus. Unlike B. motovehiculus, however, PCE SSF retains only Complex II and the NuoE/NuoF subunits of the electron transport chain and lacks a mitochondrial genome. Together, these features indicate an atypical and reduced mitochondrial metabolism, highlighting the diversity of evolutionary solutions to anaerobic energy metabolism in eukaryotes.

genomics↗

Targeted CRISPRi screening reveals unexpected resilience across the RNA polymerase III transcriptome

Increased RNA polymerase III (Pol III) activity and tRNA abundance are widely linked to cancer cell growth, yet the functional requirement for individual Pol III genes and core components remains unclear, in part due to the difficulty of achieving gene-specific perturbation of highly conserved loci. Here, we developed an inducible CRISPR interference platform and a custom single-guide RNA (sgRNA) library enabling gene-specific targeting of Pol III-transcribed genes and Pol III machinery. Genome-wide screening identified several Pol III dependencies in diploid fibroblasts and HEK293T cells, including multiple initiator methionine tRNA genes among the strongest fitness dependencies. Unexpectedly, glioblastoma models remained largely insensitive to repression of both individual Pol III genes and core Pol III components, despite efficient target repression. These findings establish a general strategy for gene-specific interrogation of conserved Pol III genes and indicate that glioblastoma models tolerate extensive perturbation of Pol III genes and machinery.

genomics↗