Publications by authors named "Yawen Bai"

Pioneer transcription factors possess the unique ability to bind to nucleosomal DNA and locally open closed chromatin, enabling the binding of additional chromatin-associated factors. These factors are pivotal in determining cell fate. Structural studies of pioneer transcription factors interacting with nucleosomes have predominantly relied on model systems incorporating canonical DNA motifs within synthetic, strongly positioned DNA.

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Woody plants, including trees, shrubs, and woody vines, are vital components of terrestrial ecosystems, playing a critical role in maintaining biodiversity, regulating climate, and supporting human livelihoods. Over the past decade, the accumulation of high-throughput sequencing, multi-omics data, and taxonomic information on woody plants has increased significantly, highlighting the need for an integrative woody plant database. Here, we present the Woody Plant Multi-Omics Database (WP-MOD, https://www.

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Understanding how animals coexist within an ecosystem is essential for the conservation of biodiversity. In China, large populations of a non-native snail Rumina decollata (a highly invasive species reported by various other countries) coexist with two native snail species (Acusta ravida and Euphaedusa aculus). However, the potential mechanisms that facilitate this non-native and native snail coexistence remain uncertain.

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Background: The ANA-grade, encompassing early-diverging angiosperm lineages, Amborellales, Nymphaeales, and Austrobaileyales, represents a fundamental phase in the evolutionary history of flowering plants. Since the completion of key assembly of the Amborella genome, the continuous influx of omics data from the lineage underscores the need for a specialized database.

Results: Here, we introduce the ANA-grade Genome Database (ANAgdb, https://anagenome.

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Article Synopsis
  • FOXA1 and GATA4 are key pioneer factors that kickstart liver cell development by attaching to the N1 nucleosome in the ALB1 gene enhancer.
  • Cryo-electron microscopy was used to analyze the structures of the N1 nucleosome and its interactions with FOXA1 and GATA4, revealing how they bind to different parts of the nucleosome and work together.
  • The study indicates that FOXA1 enhances GATA4's ability to bind by repositioning the nucleosome, which helps regulate liver cell function-related genes by making the chromatin more accessible.
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  • Chromatin fibers are organized hierarchically, with the 30-nm fibers serving as a key structure that helps regulate gene expression and maintains a dormant state for transcription.
  • The study presents a detailed structure of the chromatin fiber, specifically the H5-bound dodecanucleosome, revealing a double helical arrangement and how linker histone H5 interacts with nucleosomes.
  • The research also investigates the interactions within tetranucleosomal units and identifies structural asymmetries in histone tails that influence the overall organization of chromatin both in lab settings (in vitro) and in living organisms (in vivo).
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  • Global warming has led to an increase in atmospheric moisture, particularly in the Arctic, but the specifics of polar precipitation events are still not well understood due to a lack of data.
  • This study uses GPM satellite data and ERA5 reanalysis data to analyze summer precipitation at the northern margin of the Eurasian region and the role of cyclone activity in influencing this precipitation.
  • Findings indicate that the northern margin experiences high precipitation, mainly from cyclonic activity, with significant differences in contributions between GPM and ERA5 data, revealing that stronger summer cyclones lead to more intense precipitation events.
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Background: Numerous models have been developed to predict acute kidney injury (AKI) after noncardiac surgery, yet there is a lack of independent validation and comparison among them.

Methods: We conducted a systematic literature search to review published risk prediction models for AKI after noncardiac surgery. An independent external validation was performed using a retrospective surgical cohort at a large Chinese hospital from January 2019 to October 2022.

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  • Pioneer transcription factors, like PU.1 and C/EBPα, play a key role in changing cell types by regulating hematopoietic stem cell differentiation.
  • The study reveals that PU.1 and C/EBPα work together to interact with nucleosomes, shifting DNA and unwrapping chromatin, which is crucial for gene accessibility.
  • A mutation in PU.1 linked to leukemia disrupts its ability to interact with nucleosomes, highlighting the importance of these interactions in maintaining normal cell function.
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Centromeric chromatin plays a crucial role in kinetochore assembly and chromosome segregation. Centromeres are specified through the loading of the histone H3 variant CENP-A by the conserved chaperone Scm3/HJURP. The N-terminus of Scm3/HJURP interacts with CENP-A, while the C-terminus facilitates centromere localization by interacting with the Mis18 holocomplex via a small domain, called the Mis16-binding domain (Mis16-BD) in fission yeast.

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Background: Intraoperative hypotension (IOH) is a common complication occurring in surgical practice. This study aims to comprehensively review the collaboration and impact of countries, institutions, authors, journals, keywords, and critical papers on intraoperative hypotension from the perspective of bibliometric, and to evaluate the evolution of knowledge structure clustering and identify research hotspots and emerging topics.

Methods: Articles and reviews related to IOH published from 2004 to 2022 were retrieved from the Web of Science Core Collection.

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Pioneer transcription factors possess the unique ability to access DNA within tightly packed chromatin structures, playing pivotal roles in cell differentiation and reprogramming. However, their precise mechanism for recognizing nucleosomes has remained mystery. Recent structural and biochemical investigations into the binding interactions between the human pioneer factor OCT4 and the LIN28B nucleosome by Sinha et al.

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Pioneer transcription factors are vital for cell fate changes. PU.1 and C/EBPα work together to regulate hematopoietic stem cell differentiation.

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Pioneer transcription factors are essential for cell fate changes by targeting closed chromatin. OCT4 is a crucial pioneer factor that can induce cell reprogramming. However, the structural basis of how pioneer factors recognize the in vivo nucleosomal DNA targets is unknown.

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Background: To compare the clinical outcomes of posterior chamber phakic intraocular lens (pIOL) implantation for non-pathological myopia and pathological myopia.

Methods: This retrospective case series study which were conducted in Beijing Tongren Eye Center between July 2017 and Oct 2021 comprised 192 eyes of 100 consecutive patients undergoing pIOL implantation. Eyes were divided into two groups based on having pathological myopia or not.

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Pioneer transcription factors are essential for cell fate changes by targeting closed chromatin. OCT4 is a crucial pioneer factor that can induce cell reprogramming. However, the structural basis of how pioneer factors recognize the nucleosomal DNA targets is unknown.

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Article Synopsis
  • Human acetyltransferases MOZ and MORF play a role in aggressive leukemias due to chromosomal translocations involving their amino terminus, but the specifics of this function were unclear.
  • Researchers identified two winged helix (WH) domains in both MOZ and MORF, which bind to DNA—particularly unmethylated CpG sequences—and promote gene transcription through H3K23 acetylation.
  • Advanced studies (like Cryo-EM and mass spectrometry) revealed the DNA-binding mechanisms of these domains, suggesting potential therapeutic approaches for diseases linked to abnormal MOZ/MORF activities.
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The family Channidae, members of which are commonly known as snakehead fish, includes 53 Channa species and three Parachanna species. In this study, we characterized mitochondrial genomes (mitogenomes) of five Channa species (C. andrao, C.

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  • Linker histone H1, along with its chaperones, is crucial for regulating gene expression by maintaining the structure of chromatin and its epigenetic state.
  • This study explores how the TAF-Iβ chaperone recognizes and interacts with the human linker histone isoform H1.10 using advanced biophysical and biochemical techniques.
  • The findings reveal that TAF-Iβ prevents H1.10 from binding to DNA by blocking its binding sites, highlighting a key structural mechanism in chaperone function.
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Background: IgA nephropathy (IgAN), which has been reported as the most prevalent glomerulonephritis globally, is the major contributor to end-stage renal diseases. This bioinformatics study aimed to explore glomerulotubular crosstalk genes and dysregulated pathways relating to the pathogenesis of IgAN.

Methods: The microarray datasets from the Gene Expression Omnibus (GEO) database were searched.

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The chromatosome, a nucleosome bound to a histone H1, is the structural unit of metazoan chromatin. Determination of the high-resolution structure of the chromatosome is challenging due to the dynamic nature of H1 binding. Here, we present a protocol for purifying an optimized single-chain antibody variable fragment (scFv) that can be used to stabilize the chromatosome for single-particle cryo-EM studies.

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Accurate chromosome segregation relies on the specific centromeric nucleosome-kinetochore interface. In budding yeast, the centromere CBF3 complex guides the deposition of CENP-A, an H3 variant, to form the centromeric nucleosome in a DNA sequence-dependent manner. Here, we determine the structures of the centromeric nucleosome containing the native CEN3 DNA and the CBF3core bound to the canonical nucleosome containing an engineered CEN3 DNA.

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The repeating structural unit of metazoan chromatin is the chromatosome, a nucleosome bound to a linker histone, H1. There are 11 human H1 isoforms with diverse cellular functions, but how they interact with the nucleosome remains elusive. Here, we determined the cryoelectron microscopy (cryo-EM) structures of chromatosomes containing 197 bp DNA and three different human H1 isoforms, respectively.

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Genomic DNA in eukaryotes is organized into chromatin through association with core histone proteins to form nucleosomes. To understand the structure and function of chromatin, we must determine the structures of nucleosomes containing native DNA sequences. However, to date, our knowledge of nucleosome structures is mainly based on the crystallographic studies of the nucleosomes containing non-native DNA sequences.

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ATP-dependent chromatin remodeling factors of SWI/SNF2 family including ISWI, SNF2, CHD1 and INO80 subfamilies share a conserved but functionally non-interchangeable ATPase domain. Here we report cryo-electron microscopy (cryo-EM) structures of the nucleosome bound to an ISWI fragment with deletion of the AutoN and HSS regions in nucleotide-free conditions and the free nucleosome at ∼ 4 Å resolution. In the bound conformation, the ATPase domain interacts with the super helical location 2 (SHL 2) of the nucleosomal DNA, with the N-terminal tail of H4 and with the α1 helix of H3.

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