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Lin, X.

Publications and source records attributed to Lin, X..

At least 217 records · Page 12Linked to original sources

Boosting wheat functional genomics via indexed EMS mutant library of KN9204

A better understanding of wheat functional genomics could facilitate the targeted breeding for agronomic traits improvement and environmental adaptation. With the release of reference genomes and extensive re-sequencing data of wheat and relatives, wheat functional genomics enters a new era. However, limited transformation efficiency in wheat hampers in-depth gene functional study and genetic manipulation for breeding. Here, we generated an EMS mutagenesis library of KN9204, a widely grown elite wheat variety in northern China, with available reference genome, transcriptome, and epigenome of various tissues. The library harbors enormous developmental diversity covering important tissues and transition stages. Exome capture sequencing of 2,090 mutant lines, with probes designed by KN9204 genome, revealed that 98.79% of coding genes have mutations and 1,383 EMS-type SNPs per line averagely. Novel allelic variations for important agronomic trait-related genes, such as Rht-D1, Q, TaTB1, and WFZP, were identified. We tested 100 lines with severe mutations in 80 NAC TFs under drought and salinity stresses, and found 13 lines with altered sensitivity. Three lines were further analyzed for the regulation insight of NAC TFs in stress response by combing transcriptome and available chromatin accessibility data. Hundreds of direct targets of NAC with altered transcriptional pattern in mutant lines under salt or drought stress induction were identified, including SNAC1, DREB2B, CML16 and ZFP182, knowing factors in abiotic stresses response. Thus, we have generated and indexed KN9204 EMS mutant library which would facilitate functional genomics study and provide resources for genetic manipulation in wheat.

plant biology↗

Reactivating Positive Personality Traits During Sleep Impacts Self-Evaluative Memories

Positive self-view is evident by a bias in favor of positive self-referential processing, as individuals tend to endorse positive characteristics over negative ones when making self-judgments. While research suggests that a positivity bias can contribute to psychological well-being, it remains unclear how to enhance positive self-referential processing. Here, we reported an integrated training procedure that aimed at enhancing individuals positive self-referential processing. Specifically, participants engaged in a cue-approach training task (CAT) during wakefulness where they gave speeded motor responses to positive personality traits. In a subsequent nap, we unobtrusively re-played half of the trained positive traits during participants slow-wave sleep to reactivate memories associated with these positive traits (targeted memory reactivation, TMR). Upon awakening, we found that CAT+TMR enhanced participants positive self-referential processing, as evidenced by faster endorsement of positive traits. Further analysis revealed that this enhancement was associated with specific brainwave patterns during sleep: delta (1-4 Hz) traveling waves moving from posterior to anterior brain regions. These findings demonstrate the potential benefits of integrated wakeful cue-approach training and sleep-based memory reactivation in strengthening positive self-referential processing.

neuroscience↗

Systematic mining and genetic characterization of regulatory factors for wheat spike development

The spike architecture of wheat plays a crucial role in determining grain number, making it a key trait to optimize in wheat breeding programs. In this study, through a multi-omic approach, we analyzed the transcriptome and epigenome profiles of the shoot apex at eight developmental stages, revealing coordinated changes in chromatin accessibility and H3K27me3 abundance during the flowering transition. We constructed a core transcriptional regulatory network (TRN) that drives wheat spike formation, and experimentally validated a multi-layer regulatory module involving TaSPL15, TaAGLG1, and TaFUL2. By integrating the TRN with genome-wide association analysis (GWAS), we identified 227 transcription factors (TFs), including 42 with known functions and 185 with unknown functions. Further investigation of 61 novel TFs using multiple homozygous mutant lines uncovered 36 TFs with altered spike architecture or flowering time, such as TaMYC2-A1, TaMYB30-A1, and TaWRKY37-A1. Of particular interest, TaMYB30-A1, downstream and repressed by WFZP, was found to regulate fertile spikelet number. Notably, during the domestication and breeding process in China, the excellent haplotype of TaMYB30-A1 containing a C allele at the WFZP binding site was enriched, leading to improved agronomic traits. Our study presents novel and high-confidence regulators and offers an effective strategy for understanding the genetic basis of wheat spike development, with practical impact for wheat breeding applications.

plant biology↗

Clinical PARP inhibitors allosterically induce PARP2 retention on DNA

PARP1 and PARP2 detect DNA breaks, which activates their catalytic production of poly(ADP-ribose) that recruits repair factors and releases PARP1/2 from DNA. PARP inhibitors (PARPi) are used in cancer treatment and target PARP1/2 catalytic activity, interfering with repair and increasing PARP1/2 persistence on DNA damage. Additionally, certain PARPi exert allosteric effects that increase PARP1 retention on DNA. However, no clinical PARPi exhibit this allosteric behavior toward PARP1. In contrast, we show that certain clinical PARPi exhibit an allosteric effect that retains PARP2 on DNA breaks in a manner that depends on communication between the catalytic and DNA-binding regions. Using a PARP2 mutant that mimics an allosteric inhibitor effect, we observed increased PARP2 retention at cellular damage sites. The new PARPi AZD5305 also exhibited a clear reverse allosteric effect on PARP2. Our results can help explain the toxicity of clinical PARPi and suggest ways to improve PARPi moving forward.

biochemistry↗

Human acute microelectrode array recordings with broad cortical access, single-unit resolution and parallel behavioral monitoring

Human single-unit studies currently rely on neurosurgical procedures that provide only limited brain coverage and on recording devices that do not integrate easily into established surgical routines. Here, we report reliable and robust acute multi-channel recordings with broad cortical access using planar microelectrode arrays (MEA) implanted intracortically in awake brain surgery. We provide a comprehensive characterization of extracellular neuronal activity acquired intraoperatively in tumor patients with large open craniotomies. MEA implantation was fast, safe and yielded high-quality signals at the microcircuit, local field potential level, and at the cellular, single-unit level. Recording from parietal association cortex, a region previously unexplored in human single-unit studies, we demonstrate applications on these complementary spatial scales and describe travelling waves of oscillatory activity as well as single-neuron and neuronal population responses during numerical cognition including operations with uniquely human number symbols. Intraoperative MEA recordings are practicable and can be scaled up to explore cellular and microcircuit mechanisms of a wide range of human brain functions.

neuroscience↗

Uncovering transcriptional regulatory network during regeneration for boosting wheat transformation

Genetic transformation is important for gene functional study and crop breeding. Though it is available in many plant species, the transformation efficiency in wheat is generally low, which greatly restricts the genetic manipulation in wheat. Here, we use multi-omic analysis strategy to uncover core transcriptional regulatory network (TRN) driving wheat shoot regeneration and identify key factors that boost the transformation efficiency. RNA-seq, ATAC-seq and CUT&Tag were used to profile the transcriptome and chromatin dynamic during regeneration process from immature embryo of wheat variety Fielder. Sequential expression of gene clusters that mediating cell fate transition during regeneration is induced by auxin signaling, in coordination with changes of chromatin accessibility, H3K27me3 and H3K4me3 status. The TRN driving wheat shoot regeneration was built-up and 446 key transcriptional factors (TFs) occupied the core of network were identified, including functionally tested regeneration factors in other species. We further compared the regeneration process between wheat and Arabidopsis and found that DNA binding with one finger (DOF) TFs show distinct patterns in two species. Furthermore, we found that TaDOF5.6 (TraesCS6A02G274000) and TaDOF3.4 (TraesCS2B02G592600) can significantly improve the transformation efficiency of different wheat varieties. Thus, our data uncovers the molecular regulatory insights for wheat shoot regeneration process and provides potential novel targets for improving transformation efficiency in wheat.

developmental biology↗

Divorce rate in birds increases with male promiscuity and migration distance

Socially monogamous animals may break up their partnership after one breeding season by a so-called divorce behaviour. Divorce rate immensely varies across avian taxa that have a predominantly monogamous social mating system. Although a range of factors associated with divorce have been tested, there is not a consensus regarding the large-scale variation and relationships among associated factors. Moreover, the impact of sexual roles in divorce still needs further investigation. Here, we applied phylogenetic comparative methods to analyze one of the largest datasets ever compiled that included divorce rates from published case studies of 232 avian species from 25 orders and 61 families. We tested correlations between divorce rate and a group of factors that are closely related to pair bond strength: promiscuity of both sexes, migration distance, and adult mortality. Our results showed that only male promiscuity, but not female promiscuity, had a critical relationship with divorce rate. Furthermore, migration distance was positively correlated with divorce rate and indirectly affected divorce rate via male promiscuity. These findings indicated that divorce might not be simply explained as an adaptive strategy or neutral occurrence, but could be a mixed response to sexual conflict and stress from the ambient environment.

ecology↗

Corticosteroid Activation of Atlantic Sea Lamprey Corticoid Receptor: Allosteric Regulation by the N-terminal Domain

Lampreys are jawless fish that evolved about 550 million years ago at the base of the vertebrate line. Modern lampreys contain a corticoid receptor (CR), the common ancestor of the glucocorticoid receptor (GR) and mineralocorticoid receptor (MR), which first appear in cartilaginous fish, such as sharks. Until recently, 344 amino acids at the amino terminus of adult lamprey CR were not present in the lamprey CR sequence in GenBank. A search of the recently sequenced lamprey germline genome identified two CR sequences, CR1 and CR2, containing the 344 previously un-identified amino acids. CR1 also contains a novel four amino acid insertion in the DNA-binding domain (DBD). We studied corticosteroid and progesterone activation of CR1 and CR2 and found their strongest response was to 11-deoxycorticosterone and 11-deoxycortisol, the two circulating corticosteroids in lamprey. Based on steroid specificity, both CRs are close to elephant shark MR and distant from elephant shark GR. HEK293 cells that were transfected with full-length CR1 or CR2 and the MMTV promoter have about 3-fold higher steroid-mediated activation compared to HEK293 cells transfected with these CRs and the TAT3 promoter. Deletion of the amino-terminal domain (NTD) of lamprey CR1 and CR2 to form truncated CRs decreased transcriptional activation by about 70% in HEK293 cells that were transfected with MMTV, but increased transcription by about 6-fold in cells transfected with TAT3. This indicated that the promoter has an important effect on NTD regulation of transcriptional activation of the CR by steroids. Our results also indicate that the entire lamprey CR sequence is needed for an accurate determination of steroid-mediated transcription.

evolutionary biology↗

Identification of a self-renewing muscle satellite cell state by single-cell chromatin accessibility profiling

A balance between self-renewal and differentiation is critical for the regenerative capacity of tissue-resident stem cells. In skeletal muscle, successful regeneration requires the orchestrated activation, proliferation, and differentiation of muscle satellite cells (MuSCs) that are normally quiescent. A subset of MuSCs undergoes self-renewal to replenish the stem cell pool, but the features that identify and define self-renewing MuSCs remain to be elucidate. Here, through single-cell chromatin accessibility analysis, we reveal the self-renewal versus differentiation trajectories of MuSCs over the course of regeneration in vivo. We identify TGFBR3 as a unique marker of self-renewing MuSCs that can be purified and efficiently contribute to regeneration after transplantation; and we show that SMAD4 and its downstream genes are genetically required for self-renewal in vivo by restricting differentiation. Our study unveils the identity and mechanisms of self-renewing MuSCs, while providing a key resource for comprehensive analysis of muscle regeneration.

cell biology↗

Animal complexity defines the functionality of synonymous mutations through mediating microRNA regulations

Most recently, Shen et al. revealed that most synonymous mutations (SMs) in yeast genes are strongly non-neutral, however, which was soon challenged by Kruglyak et al. who find no evidence for deleterious effect on fitness of SMs in yeast genes. We previously revealed that SMs in numerous human genes show functionality through changing miRNA regulations. Given that higher animals show higher complexity of miRNA regulations, here we present a hypothesis that SMs in lower animal genes show less functionality and vice versa. To confirm this, we comprehensively investigated the SMs changing miRNA regulations in yeast, C.elegans, Drosophila, mouse, and human. As expected, the result showed that the proportion of SMs affecting gene functionality through altering miRNA regulations is about 0%, 14%, 16%, 51%, and 60% in yeast, C. elegans, Drosophila, mouse, and human, respectively, suggesting that the complexity of animals indeed determines the functionality of SMs through mediating miRNA regulations. Finally, this study supports no evidence that most SMs in yeast genes are deleterious.

bioinformatics↗

FAVOR: Functional Annotation of Variants Online Resource and Annotator for Variation across the Human Genome

Large-scale whole genome sequencing (WGS) studies and biobanks are rapidly generating a multitude of coding and non-coding variants. They provide an unprecedented resource for illuminating the genetic basis of human diseases. Variant functional annotations play a critical role in WGS analysis, result interpretation, and prioritization of disease- or trait-associated causal variants. Existing functional annotation databases have limited scope to perform online queries or are unable to functionally annotate the genotype data of large WGS studies and biobanks for downstream analysis. We develop the Functional Annotation of Variants Online Resources (FAVOR) to meet these pressing needs. FAVOR provides a comprehensive online multi-faceted portal with summarization and visualization of all possible 9 billion single nucleotide variants (SNVs) across the genome, and allows for rapid variant-, gene-, and region-level online queries. It integrates variant functional information from multiple sources to describe the functional characteristics of variants and facilitates prioritizing plausible causal variants influencing human phenotypes. Furthermore, a scalable annotation tool, FAVORannotator, is provided for functionally annotating and efficiently storing the genotype and variant functional annotation data of a large-scale sequencing study in an annotated GDS file format to facilitate downstream analysis. FAVOR and FAVORannotator are available at https://favor.genohub.org.

genetics↗

Wastewater Influent Microbial Immigration and Contribution to Resource Consumption in Activated Sludge Using Taxon-Specific Mass-Flow Immigration Model

Wastewater influent microorganisms are part of the total chemical oxygen demand (COD) and affect the activated sludge (AS) microbial community. Precise modeling of AS processes requires accurate quantification of influent microorganisms, which is missing in many AS models (ASMs). In this study, influent microorganisms in COD unit were determined using a fast quantification method based on DNA yield and was compared with conventional respirometry method. The actively growing influent microorganisms were identified. A mass-flow immigration model was developed to quantify the influent-to-AS immigration efficiency (mi) of specific taxon i using mass balance and 16S rRNA gene high-throughput sequencing data. The modelled average m was 0.121-0.257 in site 1 (LaPrairie), and 0.050-0.126 in site 2 (Pincourt), which were corrected to 0.111-0.186 and 0.048-0.109 respectively using a constrain of mi [&le;] 1. The model was further developed to calculate contributions to organic substrate consumption by specific taxa. Those genera with zero or negative net growth rates were not completely immigration dependent (mi < 1) and contributed to 2.4% - 5.4% of the substrate consumption. These results suggest that influent microbiome may be important contributors to AS microbiome assembly and system performance (substrate consumption), which may help to improve future AS process modelling and design. SynopsisInfluent microbial immigration lacks detailed taxon-specific quantification. This study presents quantitative methods and models for influent biomass, mass-flow immigration model, and resource consumption in activated sludge. Graphic Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=106 SRC="FIGDIR/small/504022v1_ufig1.gif" ALT="Figure 1"> View larger version (30K): org.highwire.dtl.DTLVardef@1d6b43forg.highwire.dtl.DTLVardef@d3b7eborg.highwire.dtl.DTLVardef@1cfaef5org.highwire.dtl.DTLVardef@1e75bdb_HPS_FORMAT_FIGEXP M_FIG C_FIG

microbiology↗

The RAM signaling pathway links morphology, thermotolerance, and CO2 tolerance in the global fungal pathogen Cryptococcus neoformans

The environmental pathogen Cryptococcus neoformans claims over 180,000 lives each year. Survival of this basidiomycete at host CO2 concentrations has only recently been considered an important virulence trait. Through screening gene knockout libraries constructed in a CO2-tolerant clinical strain, we found mutations leading to CO2 sensitivity are enriched in pathways activated by heat stress, including calcineurin, Ras1-Cdc24, cell wall integrity, and Regulator of Ace2 and Morphogenesis (RAM). Overexpression of Cbk1, the conserved terminal kinase of the RAM pathway, partially restored defects of these mutants at host CO2 or temperature levels. In ascomycetes such as Saccharomyces cerevisiae and Candida albicans, transcription factor Ace2 is an important target of Cbk1, activating genes responsible for cell separation. However, no Ace2 homolog or any downstream component of the RAM pathway has been identified in basidiomycetes. Through in vitro evolution and comparative genomics, we characterized mutations in suppressors of cbk1{Delta} in C. neoformans that partially rescued defects in CO2 tolerance, thermotolerance, and morphology. One suppressor is the RNA translation repressor Ssd1, which is highly conserved in ascomycetes and basidiomycetes. The other is a novel ribonuclease domain-containing protein, here named PSC1, which is present in basidiomycetes and humans but surprisingly absent in most ascomycetes. Loss of Ssd1 in cbk1{Delta} partially restored cryptococcal ability to survive and amplify in the inhalation and intravenous murine models of cryptococcosis. Our discoveries highlight the overlapping regulation of CO2 tolerance and thermotolerance, the essential role of the RAM pathway in cryptococcal adaptation to the host condition, and the potential importance of post-transcriptional control of virulence traits in this global pathogen.

microbiology↗

The Solanum americanum pangenome and effectoromics reveal new resistance genes against potato late blight

Late blight caused by the oomycete pathogen Phytophthora infestans continues to cause major worldwide losses in potato and tomato. Most accessions of Solanum americanum, a globally distributed, wild Solanaceae plant, are highly resistant to late blight. We generated high-quality reference genomes of four S. americanum accessions, re-sequenced 52 accessions, and we defined variation in the NLR immune receptor genes (the S. americanum NLRome). We further screened for variation in recognition of [~]315 P. infestans RXLR effectors in 52 S. americanum accessions. Using these genotypic and phenotypic data, we cloned three novel NLR-encoding genes Rpi-amr4, Rpi-amr16 and Rpi-amr17, and determined their corresponding RXLR effector genes Avramr4 (PITG_22825), Avramr16 (PITG_02860) and Avramr17 (PITG_04373) from P. infestans. These genomic resources and methodology will support efforts to convert potato into a "nonhost" of late blight and can be applied to diseases of other crops.

plant biology↗

Drosophila cap-binding protein eiF4EHP promotes translation via a 3'UTR-dependent mechanism under hypoxia and contributes to fruit fly adaptation to oxygen variations

Hypoxia induces profound modifications in gene expression program enabling eukaryotic cells to adapt to lowered ATP supply resulting from the blockade of oxidative phosphorylation. One major consequence of oxygen deprivation is the massive repression of protein synthesis, leaving a limited set of mRNAs to be translated. D. melanogaster is strongly resistant to oxygen fluctuations, however the mechanisms allowing specific mRNA to be translated in hypoxia are still unknown. Here, we show that Ldh mRNA encoding lactate dehydrogenase is highly translated in hypoxia by a mechanism involving its 3 untranslated region. Furthermore, we identified the cap-binding protein eiF4HP as a main factor involved in 3UTR-dependent translation under hypoxia. In accordance with this observation, we show that eiF4EHP is necessary for Drosophila development under low oxygen concentrations and contributes to Drosophila mobility after hypoxic challenge. Altogether, our data bring new insight into mechanisms contributing to Drosophila adaptation to oxygen variations.

molecular biology↗

Organic Electrochemical Transistor as an On-site Signal Amplifier for Electrochemical Aptamer-based Sensing

Electrochemical aptamer-based (E-AB) sensors are typically deployed as individual, passive, surface-functionalized electrodes, but they exhibit limited sensitivity especially when the area of the electrode is reduced for miniaturization purposes. We demonstrated that organic electrochemical transistors (OECTs), electrolyte gated tran-istors with volumetric gating, can serve as on-site amplifiers to improve the sensitivity of single electrode-based E-AB sensors. By monolithically integrating an Au working/sensing electrode, on-chip Ag/AgCl reference electrode and Poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS) counter electrode -- also serving as the OECT channel, we can simultaneously perform OECT testing and traditional electroanalytical measurement on E-AB sensors including cyclic voltammetry (CV) and square-wave voltammetry (SWV). This device can directly amplify the current from the E-AB sensor via the in-plane current modulation in the counter electrode/transistor channel. The integrated OECT-based E-AB sensor is able to sense transforming growth factor beta 1 (TGF-{beta}1) with 3 to 4 orders of magnitude enhancement of sensitivity compared to that in a single electrode-based E-AB sensor (292 {micro}A/dec vs. 85 nA/dec for OECT vs. single electrode SWV). This approach is believed to be universal, which can be applied to a wide range of tethered electrochemical reporter-based sensors to enhance sensitivity, aiding in sensor miniaturization and easing the burden on backend signal processing.

bioengineering↗

Impaired bone strength and bone microstructure in a novel early-onset osteoporotic rat model with a clinically relevant PLS3 mutation

Osteoporosis is a highly prevalent disorder with a strong genetic component. Recent studies identify PLS3 as a novel bone regulator of bone metabolism and PLS3 mutations lead to a rare monogenic early-onset osteoporosis. However, the mechanism of PLS3 mutation leading to osteoporosis is unknown with no animal models carrying patient-derived PLS3 mutations generated. The effective treatment strategies for PLS3-related have not been established. Here we have constructed a novel rat model with clinically relevant hemizygous E10-16del mutation of PLS3 (PLS3E10-16del/0) that recapitulate the osteoporotic phenotypes with obviously thinner cortical thickness, significant decreases in yield load, maximum load, and breaking load of femora at 3, 6, 9 months compared to WT rats. Histomorphometric analysis indicates a significantly lower mineral apposition rate in PLS3E10-16del/0rats. Treatment with alendronate (ALN, 1.0 ug/kg per day) or teriparatide (TPTD, 40ug/kg five times weekly) for 8 weeks significantly improved bone mass and bone microarchitecture, and bone strength was significantly increased after TPTD treatment (P < 0.05). Thus, our results indicate the roles of PLS3 in the regulation of bone microstructure and bone strength, providing a novel animal model for the study of early-onset osteoporosis. Alendronate and teriparatide treatment could be a potential treatment for early-onset osteoporosis induced by PLS3 mutation.

genetics↗

Loss-of-function mutation in human Oxidation Resistance gene 1 disrupts the spatial-temporal regulation of histone arginine methylation in early brain development

We report a loss-of-function mutation in the TLDc domain of human Oxidation Resistance 1 (OXR1) gene, resulting in early-onset epilepsy, developmental delay, cognitive disabilities, and cerebellar atrophy. Patient lymphoblasts show impaired cell survival, proliferation, and hypersensitivity to oxidative stress. These phenotypes are rescued by TLDc domain replacement. We generated patient derived induced pluripotent stem cells (iPSCs) revealing impaired neural differentiation along with dysregulation of genes essential for neurodevelopment. We identified that OXR1 influences histone arginine methylation by activating protein arginine methyltransferases (PRMTs), suggesting OXR1 dependent mechanisms regulating gene expression during neurodevelopment. We modeled the function of OXR1 in early human brain development using patient derived brain organoids revealing that OXR1 contributes to the spatial-temporal regulation of histone arginine methylation in specific brain regions. Our work provides new insights into pathological features and molecular underpinnings associated with OXR1 deficiency, highlighting the therapeutic potential of OXR1 in numerous neurodegenerative and neurodevelopmental disorders.

pathology↗