bioRxiv Science⌕ Search

bioRxiv · 10.64898/2026.03.09.710545

Diverse processes drive the origination and maturation of super-enhancers and super-silencers during a vast evolutionary timescale of the bicistronic gene SMIM45

Abstract

A central question in molecular genetics concerns how transcriptional regulatory sequences and de novo genes originate and reach evolutionary fixation. In this study, we utilize the human bicistronic gene SMIM45 as a model to analyze the evolutionary trajectories of gene development. This locus comprises several functional units: three enhancers (one featuring an embedded silencer), an exonic silencer that partially overlaps an ORF, a highly conserved ancestral sequence encoding a 68-aa microprotein, and a human-specific de novo gene encoding a 107-aa protein expressed spatiotemporally in embryonic brain tissues. We identify significant disparities in formation mechanisms; for example, the NANOG hESC enhancer originated simply via two Alu insertions that constitute the regulatory element. In contrast, the exonic silencer (ATAC-STARR-seq lymphoblastoid silent region 13815), a distinct, novel type of silencer, originated by a combination of diverse mechanisms, including a "cultivator gene" process of base pair fixation consistent with the Cultivator Model proposed by Li Zhao and coworkers. Consequently, SMIM45 exemplifies novel mechanisms of regulatory element development that occurred over several hundred million years, culminating in the birth of a human-specific de novo 107-aa cistron. The properties of these super-enhancers and super-silencers suggest a complex, intricate regulation of the 107-aa protein in fetal tissues. HighlightsSMIM45, a bicistronic gene developed an array of enhancers and silencers over several hundred million years of evolution. Enhancers and silencers formed by diverse processes during very different evolutionary time frames. The silencer ATAC-STARR-seq lymphoblastoid silent region 13815 in SMIM45 appears novel, as it is composed of two distinct segments that exhibit disparate origins and developmental pathways. This intricate regulatory apparatus points to a complex regulation of the 107-aa protein gene expressed in human embryonic brain tissues.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Delihas, N.. 2026-03-13. Diverse processes drive the origination and maturation of super-enhancers and super-silencers during a vast evolutionary timescale of the bicistronic gene SMIM45. https://doi.org/10.64898/2026.03.09.710545

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

KEEP EXPLORING

Related preprints

Large language model-based bibliometric evaluation of population descriptors in human genetics

As the use of population descriptors such as race, ethnicity, and ancestry have become increasingly common in modern genetics research, there have been growing calls to critically examine their use. Most notably, in 2023, the National Academies of Science, Engineering, and Medicine (NASEM) published a report titled Using Population Descriptors in Genetics and Genomics Research: A New Framework for an Evolving Field, which included eight specific and actionable recommendations for researchers to implement the ethical and accurate use of population descriptors in genetic research. Here, we use the 2023 NASEM report as a benchmark to analyze the use of population descriptors in genome-wide association studies (GWAS). We develop a general toolkit for large language model-based bibliometrics, operationalize the report's recommendations into an evaluation framework, and apply this framework to evaluate all 4,007 papers from the GWAS Catalog published between 2007 and 2025 with full text available on PubMedCentral. We find significant improvements in adherence to NASEM report recommendations over time. However, most improvements predate the publication of the NASEM report itself, suggesting the report functioned primarily as a synthesis of existing best practices rather than a catalyst for change. We conclude by highlighting opportunities for growth in the field of human genetics.

genetics↗

Mitigating biases of rescaling in forward-in-time population genetic simulations

Forward-in-time population genetic simulations are widely used in evolutionary analyses, but simulating large populations and long genomic regions remains computationally demanding. To reduce this cost, parameter rescaling is widely employed, in which the original evolutionary process is approximated by one with a smaller population size and fewer generations. Recently, several studies using the SLiM simulator have raised concerns about the accuracy of this rescaling approach. In this study, we show that many of the biases reported in these studies can be mitigated by using a different simulation algorithm. These results reveal that the accuracy of parameter rescaling depends on how well the simulation algorithm preserves diffusion-limit properties under rescaling.

genetics↗

OPA1 controls mitochondrial dysfunction-driven liver fibrosis in MASLD

Progressive hepatic fibrosis is the principal determinant of morbidity and mortality in metabolic dysfunction-associated steatotic liver disease and steatohepatitis (MASLD/MASH). Mitochondrial dysfunction is a hallmark of MASH, and the release of mitochondrial damage-associated molecular patterns (mito-DAMPs) from injured hepatocytes can promote fibrosis. However, how mitochondrial dynamics and quality control shape the fibrotic response in MASLD/MASH remains unclear. Here, through large-scale genomic analyses of mitochondrial genes governing mitophagy, fusion and fission in human MASLD, with a power-equivalent sample size of approximately 700,000 individuals, we identify a strong association between hepatic fibrosis and the mitochondrial fusion factor dynamin-like GTPase optic atrophy 1 (OPA1). OPA1 transcripts and protein abundance in the liver epithelium were progressively dysregulated with advancing fibrosis. In mice, hepatocyte-specific OPA1 loss alone was sufficient to induce hepatic stellate cell activation and fibrosis in zone 3, promoted the release of mito-DAMPs into the circulation and exacerbated fibrosis in experimental MASH. These findings identify OPA1 as a central regulator of the hepatic fibrotic response and connect defective mitochondrial homeostasis to mito-DAMP release, hepatic stellate cell activation and fibrosis in MASLD.

genetics↗