Publications by authors named "Huanming Yang"

Chromothripsis, a hallmark of cancer, is characterized by extensive and localized DNA rearrangements involving one or a few chromosomes. However, its genome-wide frequency and characteristics in urothelial carcinoma (UC) remain largely unknown. Here, by analyzing single-regional and multi-regional whole-genome sequencing (WGS), we present the chromothripsis blueprint in 488 UC patients.

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The Human Cell Atlas (HCA) is a global partnership "to create comprehensive reference maps of all human cells-the fundamental units of life - as a basis for both understanding human health and diagnosing, monitoring, and treating disease." ( https://www.humancellatlas.

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  • The study examines the urinary microbiome's role in health and disease by analyzing a large cohort of 1,579 Chinese individuals using advanced sequencing techniques.
  • Researchers identified five unique microbial profiles, known as "urotypes," and found that gender and sex hormones significantly influence these microbiomes.
  • Additionally, the study revealed 43 genetic associations linked to specific urinary bacteria, underscoring the complex relationship between host genetics and microbiome composition.
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Ovarian cancer is the second leading cause of gynecologic cancer death worldwide, with only 20% of cases detected early due to its elusive nature, limiting successful treatment. Most deaths occur from the disease progressing to advanced stages. Despite advances in chemo- and immunotherapy, the 5-year survival remains below 50% due to high recurrence and chemoresistance.

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  • Monitoring biochemical changes during pregnancy is crucial for the health of both mothers and babies, enabling early intervention for potential issues.
  • A genetic analysis of over 20,000 Chinese women identified 410 trait-locus associations related to pregnancy, with many being newly discovered associations.
  • The research highlighted important biological pathways involved in pregnancy, such as hormone regulation and immune response, furthering our understanding of how genetics influence pregnancy outcomes and maternal health.
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  • Metabolites are crucial for monitoring health and therapeutic targets, yet their genetic influences during pregnancy remain largely unexplored.
  • A genome-wide association study was conducted using genetic data from 34,394 pregnant Chinese women, identifying 53 metabolite-gene associations, with 23 being new findings.
  • The research uncovered significant gene-environment interactions during pregnancy, with half of the associations showing pleiotropy and potential causal links between maternal metabolites and various human traits and diseases.
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Glycemic traits are critical indicators of maternal and fetal health during pregnancy. We performed genetic analysis for five glycemic traits in 14,744 Chinese pregnant women. Our genome-wide association study identified 25 locus-trait associations, including established links between gestational diabetes mellitus (GDM) and the genes CDKAL1 and MTNR1B.

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  • Respiratory diseases affect people worldwide and studies suggest there are notable differences in how men and women experience respiratory infections, potentially linked to the nasal microbiome.
  • This research analyzed the nasal microbiome of 1,593 healthy young adults using advanced sequencing methods, creating a detailed catalog of nasal bacteria and fungi.
  • The findings revealed significant sex differences in the nasal microbiome, with women showing greater ecological stability, which could provide insights into why respiratory diseases present differently in men and women.
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  • The study analyzes extrachromosomal circular DNA (eccDNA) in 80 patients with urothelial bladder carcinoma (UBC) to understand its role in genetic variability of the cancer.* -
  • Using advanced sequencing techniques, the researchers discovered a diverse and extensive presence of eccDNAs, including chimeric forms that impact gene expression and correlate with cancer markers like hypermutation and oncogene amplification.* -
  • The findings contribute a detailed map of eccDNA in UBC, providing new resources and tools for future research in cancer genetics.*
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  • - Neovaginas can be surgically created for women with MRKH syndrome or during gender-affirming surgery, and studying their microbiota is essential for effective management.
  • - A longitudinal study showed that the neovaginal microbiota initially had random characteristics with an increase in Enterococcus faecalis and Mycoplasmas, but evolved to resemble a normal vagina within 6-12 months after surgery.
  • - By 2-4 years post-surgery, the neovaginal microbiota aligned more closely with pre-surgery microbiota, particularly with the presence of Lactobacillus crispatus, indicating its association with vaginal health and opportunities for enhancing its colonization.
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  • Scientists found a lot of tiny living things called microbes in the ocean, gathering over 43,000 genomes to study.
  • They discovered new tools that could help fight bacteria, like a special CRISPR system and some substances that kill germs.
  • This research shows how the variety of microbes in the ocean can help us create new technology and medicine that can benefit us in the future.
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Introduction: Citrus is one of the most important fruit crops worldwide, and the root-associated microbiota can have a profound impact on tree health and growth.

Methods: In a collaborative effort, the International Citrus Microbiome Consortium investigated the global citrus root microbiota with samples collected from nine citrus-producing countries across six continents. We analyzed 16S rDNA and ITS2 amplicon sequencing data to identify predominant prokaryotic and fungal taxa in citrus root samples.

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The Lachnospiraceae family holds promise as a source of next-generation probiotics, yet a comprehensive delineation of its diversity is lacking, hampering the identification of suitable strains for future applications. To address this knowledge gap, we conducted an in-depth genomic and functional analysis of 1868 high-quality genomes, combining data from public databases with our new isolates. This data set represented 387 colonization-selective species-level clusters, of which eight genera represented multilineage clusters.

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  • - This study focused on a large family with multiple neurodegenerative disease symptoms not previously documented, examining the potential genetic causes through physical exams and brain imaging.
  • - Researchers found a rare mutation (E795V) in the CARS gene that appeared to correlate with the disease symptoms seen in the affected family members, decreasing aminoacylation activity by 20%.
  • - The results provide new insights into the genetic factors contributing to neurodegenerative conditions like Parkinsonism and spinocerebellar ataxia, highlighting a previously unexplored pathway in these diseases.
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Insight into associations between the gut microbiome with metabolism and aging is crucial for tailoring interventions to promote healthy longevity. In a discovery cohort of 10,207 individuals aged 40-93 years, we used 21 metabolic parameters to classify individuals into five clusters, termed metabolic multimorbidity clusters (MCs), that represent different metabolic subphenotypes. Compared to the cluster classified as metabolically healthy (MC1), clusters classified as 'obesity-related mixed' (MC4) and 'hyperglycemia' (MC5) exhibited an increased 11.

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  • Aneuploidy is a common issue in early human embryos and is a major reason for early pregnancy failures, but its effects on cell function are not well understood.
  • Researchers analyzed 14,908 single cells from 203 human blastocysts, discovering that nearly all had four distinct cell lineages, with significant gene expression changes due to aneuploidy.
  • The study revealed that aneuploidy leads to widespread changes in gene activity, with particularly notable effects on cell death and developmental instability, highlighting the importance of certain signaling pathways in embryo development.
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The incidence of young-onset colorectal cancer (yCRC) has been increasing in recent decades, but little is known about the gut microbiome of these patients. Most studies have focused on old-onset CRC (oCRC), and it remains unclear whether CRC signatures derived from old patients are valid in young patients. To address this, we assembled the largest yCRC gut metagenomes to date from two independent cohorts and found that the CRC microbiome had limited association with age across adulthood.

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The pharyngeal endoderm, an innovation of deuterostome ancestors, contributes to pharyngeal development by influencing the patterning and differentiation of pharyngeal structures in vertebrates; however, the evolutionary origin of the pharyngeal organs in vertebrates is largely unknown. The endostyle, a distinct pharyngeal organ exclusively present in basal chordates, represents a good model for understanding pharyngeal organ origins. Using Stereo-seq and single-cell RNA sequencing, we constructed aspatially resolved single-cell atlas for the endostyle of the ascidian .

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Unlabelled: The electric catfish (), belonging to the family Malapteruridae, order Siluriformes (Actinopterygii: Ostariophysi), is one of the six branches that has independently evolved electrical organs. We assembled a 796.75 Mb genome and anchored 88.

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  • - The study investigates the relationship between the human genome and nasal microbiota, finding that specific genetic factors significantly influence the diversity and composition of nasal microbes in 1,401 healthy individuals.
  • - Researchers identified 63 key genetic loci associated with nasal microbiota, including two notable loci linked to specific bacterial genera and families, with implications for both respiratory and cardiometabolic/neuropsychiatric diseases.
  • - Functional analysis revealed that the associated genes are primarily active in the nasal epithelium and involved in important signaling pathways, while further analysis indicated certain bacteria's potential causal effects on cardiometabolic health indicators.
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  • This study investigates why females generally have longer lifespans than males, revealing that genetic factors linked to longevity are more significant in females based on extensive analysis of data from centenarians in China.
  • The research highlights that findings are consistent across various regions in China and are supported by analyses involving a large dataset of over 5,000 centenarians, indicating a potentially global pattern in genetic associations with longevity.
  • The study suggests moving away from a "one-size-fits-all" approach in healthcare, encouraging tailored medical interventions that account for sex-based genetic differences and their impacts on health outcomes.
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In nature, metabolic pathways are often organized into complex structures such as multienzyme complexes, enzyme molecular scaffolds, or reaction microcompartments. These structures help facilitate multi-step metabolic reactions. However, engineered metabolic pathways in microbial cell factories do not possess inherent metabolic regulatory mechanisms, which can result in metabolic imbalance.

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Analyses of inequalities related to prevention and cancer therapeutics/care show disparities between countries with different economic standing, and within countries with high Gross Domestic Product. The development of basic technological and biological research provides clinical and prevention opportunities that make their implementation into healthcare systems more complex, mainly due to the growth of Personalized/Precision Cancer Medicine (PCM). Initiatives like the USA-Cancer Moonshot and the EU-Mission on Cancer and Europe's Beating Cancer Plan are initiated to boost cancer prevention and therapeutics/care innovation and to mitigate present inequalities.

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The Synthetic Yeast Genome Project (Sc2.0) is an international collaboration that aims to create and optimize synthetic versions of each chromosome, with the ultimate goal of assembling a yeast organism with a synthetic with design features facilitating applications in synthetic biology and engineering projects. The consortium research groups are global, and, here, we highlight the work of the China-based Sc2.

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Aneuploidy compromises genomic stability, often leading to embryo inviability, and is frequently associated with tumorigenesis and aging. Different aneuploid chromosome stoichiometries lead to distinct transcriptomic and phenotypic changes, making it helpful to study aneuploidy in tightly controlled genetic backgrounds. By deploying the engineered SCRaMbLE (synthetic chromosome rearrangement and modification by loxP-mediated evolution) system to the newly synthesized megabase Sc2.

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