Publications by authors named "Yanhui Liang"

Article Synopsis
  • The CRISPR/Cas9 gene-editing system shows promise for treating genetic diseases, but concerns about safety—especially with guide-free Cas9—exist due to potential genomic instability.
  • Research using pigs showed that guide-free Cas9 can cause genomic damage and changes in gene expression, with harmful effects correlating to the levels of Cas9 protein.
  • Long-term expression of Cas9 in pigs resulted in weight loss and increased mutations, suggesting higher risks for genomic damage and tumor development, highlighting the need for careful safety assessments before clinical use of CRISPR/Cas9.
View Article and Find Full Text PDF

Despite its remarkable potential for transforming low-resolution images, deep learning faces significant challenges in achieving high-quality superresolution microscopy imaging from wide-field (conventional) microscopy. Here, we present X-Microscopy, a computational tool comprising two deep learning subnets, UR-Net-8 and X-Net, which enables STORM-like superresolution microscopy image reconstruction from wide-field images with input-size flexibility. X-Microscopy was trained using samples of various subcellular structures, including cytoskeletal filaments, dot-like, beehive-like, and nanocluster-like structures, to generate prediction models capable of producing images of comparable quality to STORM-like images.

View Article and Find Full Text PDF

Cas9 protein without sgRNAs can induce genomic damage at the cellular level . However, whether the detrimental effects occur in embryos after Cas9 treatment remains unknown. Here, using pig embryos as subjects, we observed that Cas9 protein transcribed from injected Cas9 mRNA can persist until at least the blastocyst stage.

View Article and Find Full Text PDF
Article Synopsis
  • Current gene expression regulation methods can't precisely control gene expression both ways, so researchers developed a new strategy that modifies the Kozak sequence to fine-tune translation levels directly.* -
  • The study focused on editing three specific nucleotides (KZ3) upstream of the translation initiation codon, finding that different variants affect translation efficiency while transcription levels remain consistent.* -
  • This approach allows for adjustable gene translation in a predictable manner, and it can be applied to the entire Kozak sequence across all protein-coding genes in eukaryotes.*
View Article and Find Full Text PDF

Base editor (BE) is a gene-editing tool developed by combining the CRISPR/Cas system with an individual deaminase, enabling precise single-base substitution in DNA or RNA without generating a DNA double-strand break (DSB) or requiring donor DNA templates in living cells. Base editors offer more precise and secure genome-editing effects than other conventional artificial nuclease systems, such as CRISPR/Cas9, as the DSB induced by Cas9 will cause severe damage to the genome. Thus, base editors have important applications in the field of biomedicine, including gene function investigation, directed protein evolution, genetic lineage tracing, disease modeling, and gene therapy.

View Article and Find Full Text PDF
Article Synopsis
  • Cas12a can process multiple sgRNAs from a single transcript, making it valuable for multiplexed base editing of multiple genes or variants.
  • Current usage of Cas12a in base editing is limited due to efficiency issues and a narrow PAM range, but improvements have been made using Lachnospiraceae bacterium Cas12a (LbCas12a) variants.
  • The newly developed cytosine and adenine base editor systems allow efficient conversions and enable multiplexed editing in somatic cells and embryos, positioning them as important tools for genetic advancement, disease research, and gene therapy.
View Article and Find Full Text PDF

Oysters and mussels are important vectors for norovirus (NoV). An efficient pretreatment method for NoV detection in oysters based on ISO 15216-2:2019 was established in our previous work, but its effectiveness for other types of shellfish remains unknown. Therefore, this study systematically compared the differences between the standard and modified ISO methods in detecting NoV for oysters and mussels.

View Article and Find Full Text PDF

Large-scale three-dimensional spatial data has gained increasing attention with the development of self-driving, mineral exploration, CAD, and human atlases. Such 3D objects are often represented with a polygonal model at high resolution to preserve accuracy. This poses major challenges for 3D data management and spatial queries due to the massive amounts of 3D objects, e.

View Article and Find Full Text PDF

3D spatial data has been generated at an extreme scale from many emerging applications, such as high definition maps for autonomous driving and 3D Human BioMolecular Atlas. In particular, 3D digital pathology provides a revolutionary approach to map human tissues in 3D, which is highly promising for advancing computer-aided diagnosis and understanding diseases through spatial queries and analysis. However, the exponential increase of data at 3D leads to significant I/O, communication, and computational challenges for 3D spatial queries.

View Article and Find Full Text PDF

The emergence of the novel GII.17 Kawasaki 2014 norovirus variant raising the interest of the public, has replaced GII.4 as the predominant cause of noroviruses outbreaks in East Asia during 2014-2015.

View Article and Find Full Text PDF

Inducible expression systems are indispensable for precise regulation and in-depth analysis of biological process. Binary Tet-On system has been widely employed to regulate transgenic expression by doxycycline. Previous pig models with tetracycline regulatory elements were generated through random integration.

View Article and Find Full Text PDF

Establishing saturated mutagenesis in a specific gene through gene editing is an efficient approach for identifying the relationships between mutations and the corresponding phenotypes. CRISPR/Cas9-based sgRNA library screening often creates indel mutations with multiple nucleotides. Single base editors and dual deaminase-mediated base editors can achieve only one and two types of base substitutions, respectively.

View Article and Find Full Text PDF

Norovirus is a major cause of acute gastroenteritis worldwide. Like the major capsid protein (VP1), the minor capsid protein (VP2) also contains a hypervariable domain. Generally, a hypervariable domain is functionally driven.

View Article and Find Full Text PDF

Background: The worldwide response towards the acute gastroenteritis epidemic was well known, but the absence of an updated systematic review of global norovirus epidemiology in cases of gastroenteritis existed. We aimed to conduct and update a systematic review and meta-analysis of studies assessing norovirus prevalence among gastroenteritis patients worldwide.

Methods: Four databases (PubMed, EMBASE, Cochrane Library, and Web of Science) were searched for epidemiological papers from 2014 to 2021 which applied the PCR method to access the prevalence of norovirus in acute gastroenteritis patients more than a full year.

View Article and Find Full Text PDF

Noroviruses are causative agents of acute nonbacterial gastroenteritis epidemics worldwide. There are various genotypes, among which the non-epidemic genotype GII.8 can cause norovirus outbreaks.

View Article and Find Full Text PDF

Foodbone norovirus (NoV) is the leading cause of acute gastroenteritis worldwide. Candidate vaccines are being developed, however, no licensed vaccines are currently available for managing NoV infections. Screening for stimulated antibodies with broad-spectrum binding activities can be performed for the development of NoV polyvalent vaccines.

View Article and Find Full Text PDF

Human norovirus (HuNoV), which is the major causative agent of acute gastroenteritis, has broad antigenic diversity; thus, the development of a broad-spectrum vaccine is challenging. To establish the relationship between viral genetic diversity and antigenic diversity, capsid P proteins and antisera of seven GI and 16 GII HuNoV genotypes were analyzed. Enzyme-linked immunosorbent assays showed that HuNoV antisera strongly reacted with the homologous capsid P proteins (with titers > 5 × 10).

View Article and Find Full Text PDF

Human norovirus is a common cause of acute gastroenteritis worldwide, and oysters have been found to be the main carriers for its spread. The lack of efficient pre-treatment methods has been a major bottleneck limiting the detection of viruses in oysters. In this study, we established a novel immunomagnetic enrichment method using polyamidoamine (PAMAM) dendrimer/SA-biotin-mediated cascade amplification for reverse transcriptase quantitative real-time polymerase chain reaction (RT-qPCR) detection.

View Article and Find Full Text PDF

Human norovirus is regarded as the leading cause of epidemic acute gastroenteritis with GII.4 being the predominant genotype during the past decades. In the winter of 2014/2015, the GII.

View Article and Find Full Text PDF

Background: Human noroviruses are one of the main causes of foodborne illnesses and represent a serious public health concern. Rapid and sensitive assays for human norovirus detection are undoubtedly necessary for clinical diagnosis, especially in regions without more sophisticated equipment.

Method: The rapid reverse transcription recombinase-aided amplification (RT-RAA) is a fast, robust and isothermal nucleic acid detection method based on enzyme reaction.

View Article and Find Full Text PDF

Patients with hereditary tyrosinemia type I (HT1) present acute and irreversible liver and kidney damage during infancy. CRISPR-Cas9-mediated gene correction during infancy may provide a promising approach to treat patients with HT1. However, all previous studies were performed on adult HT1 rodent models, which cannot authentically recapitulate some symptoms of human patients.

View Article and Find Full Text PDF