Biology subjects

She, Q.

Publications and source records attributed to She, Q..

22 records · Page 2Linked to original sources

bioRxiv2020

Negative interplay between biofilm formation and competence in the environmental strains of Bacillus subtilis

Environmental strains of the soil bacterium Bacillus subtilis have valuable applications in agriculture, industry, and biotechnology. They are capable of forming robust biofilms and demonstrate excellent biological control activities in plant protection. However, environmental strains are genetically less accessible, a sharp contrast to the laboratory strains well known for their natural competence and a limitation toward their application. In this study, we observed that robust biofilm formation of the environmental strains greatly reduces the rate of competent cells within the biofilm. By using the model strain 3610, we reveal a cross-pathway regulation that allows biofilm matrix producers and competence-developing cells to undergo mutually exclusive cell differentiation. We show that the competence activator ComK represses the key biofilm regulatory gene sinI by directly binding to the sinI promoter, thus blocking competent cells from simultaneously becoming matrix producers. In parallel, the biofilm activator SlrR represses competence through three distinct mechanisms, involving both genetic regulation and cell morphological changes. We discuss potential implications of limiting competence in a bacterial biofilm. ImportanceThe soil bacterium Bacillus subtilis is capable of forming robust biofilms, a multicellular community important for its survival in the environment. B. subtilis also exhibits natural competence, the ability of cells to acquire genetic materials directly from the environment. By investigating competence development in situ during B. subtilis biofilm formation, we reveal that robust biofilm formation, an important feature of the environmental strains of B. subtilis, often greatly reduces the rate of competent cells within the biofilm. We characterize a cross-pathway regulation that allows cells associated with these two developmental events to undergo mutually exclusive cell differentiation during biofilm formation. Finally, we discuss potential biological implications of limiting competence in a bacterial biofilm.

microbiology↗

bioRxiv2019

Characterization of a novel type III effector provides new insights into the allosteric activation and suppression of the Cas10 DNase

Antiviral defense by type III CRISPR-Cas systems relies on two distinct activities of their effectors: the RNA-activated DNA cleavage and synthesis of cyclic oligoadenylate. Both activities are featured as indiscriminate nucleic acid cleavage and subjected to the spatiotemporal regulation. To yield further insights into the involved mechanisms, we reconstituted LdCsm, a lactobacilli III-A system in Escherichia coli. Upon activation by target RNA, this immune system mediates robust DNA degradation but lacks the synthesis of cyclic oligoadenylates. Mutagenesis of the Csm3 and Cas10 conserved residues revealed that Csm3 and multiple structural domains in Cas10 function in the allosteric regulation to yield an active enzyme. Target RNAs carrying various truncations in the 3' anti-tag were designed and tested for their influence on DNA binding and DNA cleavage of LdCsm. Three distinct ternary LdCsm complexes were identified. In particular, binding of target RNAs carrying a single nucleotide in the 3' anti-tag to LdCsm yielded an active LdCsm DNase regardless whether the nucleotide shows a mismatch, as in the cognate target RNA (CTR), or a match in the noncognate target RNAs (NTR), to the 5 tag of crRNA. In addition, further increasing the number of 3' anti-tag in CTR facilitated the substrate binding and enhanced the substrate degradation whereas doing the same as in NTR gradually decreased the substrate binding and eventually shut off the DNA cleavage by the enzyme. Together, these results provide the mechanistic insights into the allosteric activation and repression of LdCsm enzymes.

molecular biology↗

bioRxiv2018

Weighted Network Density Predicts Range of Latent Variable Model Accuracy

Current experimental techniques impose spatial limits on the number of neuronal units that can be recorded in-vivo. To model the neural dynamics utilizing these sampled data, Latent Variable Models (LVMs) have been proposed to study the common unobserved processes within the system that drives neural activities, through an implicit network with hidden states. Yet, relationships between these latent variable models and widely-studied network connectivity measures remained unclear. In this paper, a biologically plausible latent variable model was first fit to neural activity recorded via 2-photon microscopic calcium imaging in the murine primary visual cortex. Graph theoretic measures were then applied to quantify network properties in the recorded sub-regions. Comparison of weighted network measures with LVM prediction accuracy shows some network measures having a strong relationship with LVM prediction accuracy, while other measures do not have a robust relationship with LVM prediction accuracy. Results show LVM will achieve high accuracy in dense networks.

neuroscience↗

bioRxiv2018

Conserved accessory proteins encoded with archaeal and bacterial Type III CRISPR-Cas gene cassettes that may specifically modulate, complement or extend interference activity

A study was undertaken to identify conserved proteins that are encoded either within, or directly adjacent to, cas gene cassettes of Type III CRISPR-Cas interference modules. These Type III modules are especially versatile functionally and have been shown to target and degrade dsDNA, ssDNA and ssRNA. In addition, the interference gene cassettes are frequently intertwined with other accessory genes, including genes encoding CARF domains, some of which are likely to be cofunctional. Using a comparative genomics approach, and defining a Type III association score accounting for coevolution and specificity of flanking genes, we identified and classified 39 new Type III associated gene families. Most archaeal and bacterial Type III modules were seen to be flanked by several accessory genes, around half of which did not encode CARF domains and remain of unknown function. Non-CARF accessory genes were found to be more diverse than their CARF counterparts, encoding nuclease, helicase, protease, ATPase, transporter and transmembrane domains and including a considerable fraction that encoded no known domains. The diversity of non-CARF Type III accessory genes found in this study suggests that additional families exist which remain undetected because of the limited number of annotated genomes currently available. The method employed is scalable for potential application on metagenomic data once automated pipelines for annotation of CRISPR-Cas systems have been developed. All accessory genes found in this study are presented online in a readily accessible and searchable format for researchers to audit their model organism of choice: http://accessory.crispr.dk.

bioinformatics↗