In the era of global climate change, estuarine ecosystems face unprecedented threats from rising temperatures and salinity intrusion. Understanding how different land-use types buffer or exacerbate these stressors is critical for biodiversity conservation. This study employs a trait-based scenario simulation model approach to predict the vulnerability of fish assemblages across mangrove and agricultural landscapes in the Irrawaddy Delta. By extracting species-specific physiological tolerance limits (thermal and salinity thresholds) and applying scenario-based predictive modeling, we simulated projected threshold exceedance risks under sequential thermal stress intervals (+0.2 to +2.0 °C). Our results reveal a stark contrast in ecosystem resilience. Fish assemblages in agricultural lands exhibited critically low Thermal Safety Margins (TSM) and experienced a rapid 100% projected loss in species richness by +1.2 °C. Conversely, natural mangrove habitats functioned as robust climate refugia, sustaining higher predicted species richness and mitigating species loss to approximately 32.5–52.4% even under severe +2.0 °C thermal stress. This high-resolution spatial vulnerability assessment provides actionable insights for spatial prioritization and coastal conservation in Myanmar.

The Irrawaddy mangrove ecosystem in Myanmar is a crucial habitat for aquatic biodiversity, yet its ecological dynamics remain understudied. This research explored the seasonal variation, spatial dynamics, and trophic structure of fish assemblages in Pyapon and Bogale townships, Myanmar. Seasonal and market surveys recorded 129 fish species from 64 families, with Mystus gulio, Oryzias dancena, Coilia dussumieri, and Glossogobius giuris dominating the community. Seasonal shifts significantly influenced species diversity. Winter exhibited the highest species richness and diversity, while summer displayed the lowest. Nevertheless, species evenness remained highly stable across all seasons, suggesting a consistently balanced community. Moving beyond basic water parameters, multivariate analyses demonstrated that habitat complexity and food web dynamics are likely key drivers of community structuring. Permutational multivariate analysis of variance revealed a highly significant spatial separation of fish assemblages between mangrove and agricultural land habitats. Furthermore, indicator species analysis identified specific taxa driving this divergence, while functional feeding guild analysis revealed a marked dominance of benthivores and detritivores in mangrove sites. This highlights the critical role of mangrove-derived organic matter in supporting the estuarine food web. The presence of four threatened species, including the Endangered Eleutheronema tetradactylum and Johnius macrorhynus, demonstrates that preserving the physical integrity and trophic inputs of mangroves is paramount for sustaining estuarine fish diversity and supporting sustainable local fisheries management.

In a study published in Cell Death and Disease on August 29, 2026, a team led by Hu Xintian and Mao Bingyu from the Kunming Institute of Zoology (KIZ) of the Chinese Academy of Sciences, along with collaborators from Kunming Medical University First Affiliated Hospital, developed a tree shrew model of Parkinson's disease by knocking out the DJ-1 gene in the substantia nigra. DJ-1 loss-of-function mutations were identified in 2003 as a Parkinson's disease risk gene in Dutch and Italian families. However, DJ-1 knockout mice failed to develop typical Parkinson's symptoms, leaving the causal relationship uncertain. The researchers chose tree shrews because they possess a caudate-putamen structure similar to humans and primates, substantia nigra neurons comparable in size to primates, and complex three-dimensional motor patterns.

In a study published in Molecular Psychiatry on September 4, 2026, a team led by Xiao Xiao from the Kunming Institute of Zoology (KIZ) of the Chinese Academy of Sciences, along with collaborators from Jinan University and Xi'an Jiaotong University First Affiliated Hospital, integrated genome-wide association study data, whole-exome sequencing data, and human brain cortical developmental multi-omics data to identify cortical cell types underlying schizophrenia genetic risk. The researchers built an atlas of approximately 3 million nuclei from 325 neurotypical donors, using 22 public single-nucleus RNA sequencing datasets. The data spanned from early embryonic development to adulthood, covering the cingulate, frontal, motor, temporal, and visual cortices.

How domestication shapes brain evolution remains an open question. In this study, we integrated single-nucleus RNA sequencing (snRNA-seq), population genomics, and machine learning to investigate hippocampal evolution under domestication. Across-species comparisons revealed that hippocampal cell type profiles are largely conserved across vertebrate species, while supporting the presence of adult hippocampal neurogenesis in birds. We further found that domestication and selective breeding likely influence the cellular composition and molecular regulation of the hippocampus. Our findings provide cellular evidence supporting the hypothesis that domestication affects adult hippocampal neurogenesis. Additionally, we showed that genes associated with neural progenitor cells (NPCs) states and cell-marker programs are enriched for signatures of selection. Many of these genes function as regulators of neurogenesis and pathways mediating stress and fear reduction. Specifically, we identified selection at the FKBP5 promoter that may influence its expression in the NPC lineage, potentially contributing to stress-response regulation during domestication. Collectively, these results suggest that domestication is associated with hippocampal remodeling as part of an adaptive response to human-managed environments. This study provides a cellular and genetic perspective on how domestication reshapes the brain and offers a basis for further investigation into the mechanisms of neural evolution within the context of microevolution.

Embryonic stem cells (ESCs) exhibit a hyperactive chromatin state at ribosomal RNA (rRNA) genes, which not only plays roles in active rRNA synthesis and ribosome biogenesis (RiBi), but also links to genome architecture. However, how this active chromatin state is maintained in ESCs remains poorly understood. Here, we identify Tcf15, a mouse ESC-specific factor, as a novel regulator of ribosomal DNA (rDNA) chromatin state. Tcf15 localizes to the nucleolus, binds the coding region of rRNA genes, and independently recruits epigenetic modifiers—either Tet2 or Rbbp5 (a core component of H3K4 methyltransferases)—to promote an active chromatin configuration. Depletion of Tcf15 increases DNA methylation and H3K27me3 levels at rDNA. Intriguingly, the Tcf15-Rbbp5 axis ensures precursor rRNA transcription and RiBi, whereas the Tcf15-Tet2 axis is not involved in rRNA synthesis. Ribosome profiling further revealed compromised translation of a subset of mRNAs involved in DNA replication, damage response, and repair. Consequently, Tcf15- or Rbbp5-deficient ESCs exhibit severe genomic instability. Our findings add a new regulatory layer of chromatin state in rDNA of stem cells, and reveal a previously unrecognized phenotypic consequence of defective RiBi in ESCs.

Pigs are not only important agricultural animals but also key model organisms for studying evolution, complex traits, and human diseases. As genome sequencing and genetic research advance, numerous genetic variants associated with pig domestication, economic traits, and disease have been identified. However, many key variants reside in non-coding regions, and traditional linear genome annotation cannot determine which genes these regulatory variants act upon. In a study published in Molecular Biology and Evolution on July 30, 2026, a team led by Prof. Zhang Yaping from the Kunming Institute of Zoology (KIZ), along with collaborators from the University of Science and Technology of China and Yunnan University, constructed Pig Matrix, a multi-omics 3D regulatory genomics database for pigs.

The complement system was originally discovered as a product of hepatocytes and immune cells secreted into circulation, mediating immune responses through the classical, lectin, and alternative pathways. However, recent findings have revealed that non-immune cells, including epithelial cells, endothelial cells, neurons, pancreatic islet cells, and fibroblasts, also express complement molecules localized to organelles such as lysosomes, endoplasmic reticulum, and mitochondria, forming an intracellular complement system independent of circulating complement. Named the "complosome," this system regulates apoptosis, metabolism, autophagy, and gene expression.

Myelin sheaths wrap neuronal axons and are essential for rapid nerve impulse conduction. Their formation depends on the proliferation, differentiation, and maturation of oligodendrocyte precursor cells (OPCs). Because myelination involves massive membrane expansion and high metabolic activity, OPCs face persistent oxidative stress. In a study published in Advanced Science, a team led by Prof. Mao Bingyu from the Kunming Institute of Zoology (KIZ), in collaboration with Prof. Zhao Shuhua's team at the First Affiliated Hospital of Kunming Medical University, revealed that the E3 ubiquitin ligase RLIM safeguards oligodendrocyte development and myelination by targeting SLC7A11 for polyubiquitination to regulate ferroptotic resistance.

DOI:https://onlinelibrary.wiley.com/doi/10.1111/acel.70603 Schematic diagram of the mechanism by which LINC01021 promotes cellular and individual aging.