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Heterosis, or hybrid vigor, is exploited by breeders to produce elite high-yielding crop lines, but beneficial phenotypes are lost in subsequent generations owing to genetic segregation. Clonal propagation through seeds would enable self-propagation of F1 hybrids. Here we report a strategy to enable clonal reproduction of F1 rice hybrids through seeds. We fixed the heterozygosity of F1 hybrid rice by multiplex CRISPR–Cas9 genome editing of the REC8, PAIR1 and OSD1 meiotic genes to produce clonal diploid gametes and tetraploid seeds. Next, we demonstrated that editing the MATRILINEAL (MTL) gene (involved in fertilization) could induce formation of haploid seeds in hybrid rice. Finally, we combined fixation of heterozygosity and haploid induction by simultaneous editing of all four genes (REC8, PAIR1, OSD1 and MTL) in hybrid rice and obtained plants that could propagate clonally through seeds. Application of our method may enable self-propagation of a broad range of elite F1 hybrid crops.

Tiller angle and leaf angle are two important components of rice (Oryza sativa) plant architecture that play a crucial role in determining grain yield. Here, we report the cloning and characterization of the Loose Plant Architecturel (LPA1) gene in rice, the functional ortholog of the AtIDD15/SHOOT GRAVITROPISM5 (SGR5) gene in Arabidopsis (Arabidopsis thaliana). LPA1 regulates tiller angle and leaf angle by controlling the adaxial growth of tiller node and lamina joint. LPA1 was also found to affect shoot gravitropism. Expression pattern analysis suggested that LPA1 influences plant architecture by affecting the gravitropism of leaf sheath pulvinus and lamina joint. However, LPA1 only influences gravity perception or signal transduction in coleoptile gravitropism by regulating the sedimentation rate of amyloplasts, distinct from the actions of LAZY1. LPA1 encodes a plant-specific INDETERMINATE DOMAIN protein and defines a novel subfamily of 28 INDETERMINATE DOMAIN proteins with several unique conserved features. LPA1 is localized in the nucleus and functions as an active transcriptional repressor, an activity mainly conferred by a conserved ethylene response factor-associated amphiphilic repression-like motif. Further analysis suggests that LPA1 participates in a complicated transcriptional and protein interaction network and has evolved novel functions distinct from SGR5. This study not only facilitates the understanding of gravitropism mechanisms but also generates a useful genetic material for rice breeding.

The clustered regularly interspaced short palindromic repeats（CRISPR）-associated endonuclease 9（CRISPR/Cas9） system has emerged as a promising technology for specific genome editing in many species. Here we constructed one vector targeting eight agronomic genes in rice using the CRISPR/Cas9 multiplex genome editing system. By subsequent genetic transformation and DNA sequencing, we found that the eight target genes have high mutation efficiencies in the T0 generation. Both heterozygous and homozygous mutations of all editing genes were obtained in T0 plants. In addition, homozygous sextuple, septuple, and octuple mutants were identified. As the abundant genotypes in T0 transgenic plants, various phenotypes related to the editing genes were observed. The findings demonstrate the potential of the CRISPR/Cas9 system for rapid introduction of genetic diversity during crop breeding.

Numbers on branches indicate bootstrap percentages for 1000 replicates. (b) Subcellular localization of MtDMP8-RFP and MtDMP9-RFP proteins in Arabidopsis leaf protoplasts; pm-GFP was used as a plasma membrane marker. Consistent with this prediction, both proteins colocalized with the PIP2A (At3g53420)-based plasma membrane marker pm-GFP (Zhu et al., 2020) when MtDMP8 and MtDMP9 were transiently expressed as red fluorescent protein (RFP) fusions in Arabidopsis leaf protoplasts (Figure 1b). The haploid plants were morphologically similar to the female parent A17 (Figure 1k). [...]the simultaneous inactivation of MtDMP8 and MtDMP9 can trigger in vivo maternal haploid induction in M. truncatula.

Polytetrafluoroethylene (PTFE) blended with polyimide (PI) and filled with boron nitride (BN) is prepared through cold pressing and sintering for composites with remarkable wear resistance and reduced coefficient of friction (COF). The characterizations show that BN and PI at different levels, improve the hardness, dynamic thermo-mechanical modulus, thermal conductivity, and tribological properties of PTFE. PI boosts the dispersion and bonding of BN in PTFE. In dry sliding friction of a block-on-ring tribometer, the wear rate and COF of 10:10:80 BN/PI/PTFE reduce to almost 1/300 and 80% of those of pure PTFE, respectively, as the wear mechanism transition from being adhesive to partially abrasive. This occurs only when the additives BN and PI induce a synergistic effect, that is, at concentrations that are not higher than ca. 10 wt% and 15 wt%, respectively. The obvious agglomeration at high percentages of added PI and severe conditions (400 N and 400 rpm) induce strong adhesive failure. The variations in the tensile properties, hardness, crystallization, and microstructure of the composites correspond to different effects. The multiple parameters of the plots of wear and friction are transformed into their contour curves. The mechanism transition maps aid in understanding the influence of various test conditions and composite compositions on the contact surfaces in the space-time framework of wear.

Summary Clustered regularly interspaced short palindromic repeats‐associated protein 9 (CRISPR‐Cas9) is a revolutionary technology that enables efficient genomic modification in many organisms. Currently, the wide use of Streptococcus pyogenes Cas9 (SpCas9) primarily recognizes sites harbouring a canonical NGG protospacer adjacent motif (PAM). The newly developed VQR (D1135V/R1335Q/T1337R) variant of Cas9 has been shown to cleave sites containing NGA PAM in rice, which greatly expanded the range of genome editing. However, the low editing efficiency of the VQR variant remains, which limits its wide application in genome editing. In this study, by modifying the single guide RNA (sgRNA) structure and strong endogenous promoters, we significantly increased the editing efficiency of the VQR variant. The modified CRISPR‐Cas9‐VQR system provides a robust toolbox for multiplex genome editing at sites containing noncanonical NGA PAM.

In this study, a series of cerium dioxide catalysts with varying hydrothermal temperatures and times were synthesized using the hydrothermal method, without the use of templates. The impact of varying hydrothermal conditions on the activity of cerium dioxide catalysts was investigated through experiments to examine their oxidation characteristics in soot combustion. Among the conditions tested, the hydrothermal conditions of 140 °C and 6 h yielded the most optimal catalytic oxidation of soot, with a combustion characteristic temperature (Tp) of 552 °C and a reduction of 122.9 °C. The integrated combustion index (S) and combustion stability coefficient (Rw) were found to be 27.97 × 108 %2min−2°C−3 and 90.76 × 105, respectively. The indices of S and Rw exhibited an improvement of 51.1% and 36.93%, respectively.

The tomato (Solanum lycopersicum) gene ASCORBATE PEROXIDASE 4 (SlAPX4), specifically induced during fruit ripening, is involved in the decrease of ascorbate. [...]analysis of mutants provided helpful information for understanding how RBOH genes regulate tomato reproduction process (Dai et al.). Additionally, manipulation of the distribution and frequency of meiotic recombination events to increase genetic diversity and disrupting genetic interference is a hot-topic in crop breeding. With the rapid development of genome editing technologies and functional genomics, it is foreseeable that many new optimized gene editing systems will emerge. Because of the limitation inherent in time constraints, this research topic did not cover the development, optimization, and application of gene editing systems for as many crops as possible.

Clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 is the third generation of novel targeted genome editing technology after zinc finger nucleases (ZFNs) and transcription activator like effector nucleases (TALENs). It is also one of the most promising techniques for mutating and modifying genes. The CRISPR-Cas9 system has the advantages of simplicity, high efficiency, high specificity, and low production cost, thus greatly promoting the study of gene function. Meanwhile, it has attracted the attention of biologists. After the development and improvement in recent years, CRISPR-Cas9 system has become increasingly mature and has been widely used in crop improvement. Firstly, this review systematically summarizes the generation and advantages of CRISPR-Cas9 system. Secondly, three derivative technologies of the CRISPR-Cas9 system are introduced. Thirdly, this review focuses on the application of CRISPR-Cas9 system in gene knockout, gene knock-in, and gene regulation, as well as the improvement of yield, quality, and biological resistance of important crops such as rice, wheat, soybean, corn, and potato. Finally, this review proposes the potential challenges of CRISPR-Cas9 system, and discusses the future development of CRISPR-Cas9 system.

Background Lung adenocarcinoma (LUAD) is a common type of lung cancer with a high risk of metastasis, but the exact molecular mechanisms of metastasis are not yet understood. Methods This study acquired single-cell transcriptomics profiling of 11 distal normal lung tissues, 11 primary LUAD tissues, and 4 metastatic LUAD tissues from the GSE131907 dataset. The lung multicellular ecosystems were characterized at a single-cell resolution, and the potential mechanisms underlying angiogenesis and metastasis of LUAD were explored. Results We constructed a global single-cell landscape of 93,610 cells from primary and metastatic LUAD and found that IGF2BP2 was specifically expressed both in a LUAD cell subpopulation (termed as LUAD_IGF2BP2), and an endothelial cell subpopulation (termed as En_IGF2BP2). The LUAD_IGF2BP2 subpopulation progressively formed and dominated the ecology of metastatic LUAD during metastatic evolution. IGF2BP2 was preferentially secreted by exosomes in the LUAD_IGF2BP2 subpopulation, which was absorbed by the En_IGF2BP2 subpopulation in the tumor microenvironment. Subsequently, IGF2BP2 improved the RNA stability of FLT4 through m 6 A modification, thereby activating the PI3K-Akt signaling pathway, and eventually promoting angiogenesis and metastasis. Analysis of clinical data showed that IGF2BP2 was linked with poor overall survival and relapse-free survival for LUAD patients. Conclusions Overall, these findings provide a novel insight into the multicellular ecosystems of primary and metastatic LUAD, and demonstrate that a specific LUAD_IGF2BP2 subpopulation is a key orchestrator promoting angiogenesis and metastasis, with implications for the gene regulatory mechanisms of LUAD metastatic evolution, representing themselves as potential antiangiogenic targets.