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ABSTRACT Actin microfilaments (F-actin) serve as the track for directional movement of organelles in plant cells. In actively growing plant cells, F-actin often form robust bundles that trespass the cellular dimension. To test how the F-actin network was employed for peroxisome movement, we wished to disturb actin organization by genetically compromising the function of villin (VLN) proteins that serve as the primary bundling factor inArabidopsis thalianacells. To do so, we isolated T-DNA insertional mutants in threeVLNgenes that were most actively expressed in vegetative tissues. We found that thevln4mutation greatly enhanced the growth defects caused by thevln2 vln3double mutant as thevln2 vln3 vln4triple mutant had a great reduction of organ growth and formed heavily deformed tissues. Both VLN2 and VLN4 proteins were detected on bundled F-actin filaments. Compared to the wild-type cells, the double and triple mutants exhibited progressively reduction of stable F-actin bundles and had fine F-actin filaments undergo rapid remodeling. The defective F-actin network did not prevent peroxisomes from taking on both rapid and slow movements along the F-actin tracks. However, we found that compromised F-actin bundling caused significant reductions in the speed of peroxisome movement and the displacement distance of peroxisome positions. Using a correlation analysis method, we also demonstrated that the complex heterogeneous peroxisome movement may be classified into clusters reflecting the directionality of peroxisome movement. The triple mutant suffered from a significant reduction of peroxisomes exhibiting long-range and linear movement. Our results provided insights into how VLN-dependent F-actin organization was coupled with the complex patterns of peroxisome movement. 

Abstract The evolutionarily conserved microspherule protein 1 (MCRS1) has diverse functions, ranging from transcriptional regulation to stabilization of microtubule minus ends in acentrosomal spindles in mammals. A previous study suggested that in the model plant Arabidopsis thaliana, inactivation of an MCRS1 homolog gene led to aborted embryogenesis. To test whether this lethality was caused solely by sporophytic defects, we used the heterozygous emb1967-1/mcrs1-1 mutant for reciprocal crosses with the wild-type plant and found that the MCRS1 gene was dispensable for the development of both male and female gametophytes. An MCRS1–GFP fusion protein was expressed in the mcrs1 mutant and suppressed the mutation as evidenced by restored growth. This functional fusion protein exclusively localized to interphase nuclei and became unnoticeable during mitosis before reappearing in the reforming daughter nuclei. Affinity purification of the MCRS1–GFP protein specifically recovered the Myb-like transcription factor DRMY1 (Development Regulated Myb-like 1) but not microtubule-associated factors. Direct MCRS1–DRMY1 interaction was also demonstrated by a localization-based assay in living cells. Thus, we hypothesized that MCRS1’s function was perhaps linked to transcription factors like DRMY1 and its paralog DP1 for regulation of gene expression during sporophyte development. 

Abstract Spindle assembly in vertebrates requires the Aurora kinase, which is targeted to microtubules and activated by TPX2 (Targeting Protein of XKLP2). In Arabidopsis (Arabidopsis thaliana), TPX2-LIKE 3 (TPXL3), but not the highly conserved TPX2, is essential. To test the hypothesis that TPXL3 regulates the function of α Aurora kinase in spindle assembly, we generated transgenic Arabidopsis lines expressing an artificial microRNA targeting TPXL3 mRNA (amiR-TPXL3). The resulting mutants exhibited growth retardation, which was linked to compromised TPXL3 expression. In the mutant cells, α Aurora was delocalized from spindle microtubules to the cytoplasm, and spindles were assembled without recognizable poles. A functional TPXL3-GFP fusion protein first prominently appeared on the prophase nuclear envelope. Then, TPXL3-GFP localized to spindle microtubules (primarily toward the spindle poles, like γ-tubulin), and finally to the re-forming nuclear envelope during telophase and cytokinesis. However, TPXL3 was absent from phragmoplast microtubules. In addition, we found that the TPXL3 N-terminal Aurora-binding motif, microtubule-binding domain, and importin-binding motif, but not the C-terminal segment, were required for its mitotic function. Expression of truncated TPXL3 variants enhanced the defects in spindle assembly and seedling growth of amiR-TPXL3 plants. Taken together, our findings uncovered the essential function of TPXL3, but not TPX2, in targeting and activating α Aurora kinase for spindle apparatus assembly in Arabidopsis. 

Nanohybrids of graphene and colloidal semiconductor quantum dots (QDs/Gr) provide a promising quantum sensing scheme for photodetection. Despite exciting progress made in QDs/Gr photodetectors in broadband from ultraviolet to short-wave infrared, the device performance is limited in middle-wave infrared (MWIR) detection. A fundamental question arises as to whether the thermal noiseinduced dark current and hence poor signal-to-noise ratio in conventional uncooled MWIR photodetectors persist in QDs/ Gr nanohybrids. Herein, we investigated noise, responsivity (R*), and specific detectivity (D*) in HgTe QDs/Gr nanohybrids, revealing that the noise and R* are decoupled in nanohybrids and each can be optimized independently toward its theoretical limit. Specifically, the noise in the QDs/Gr nanohybrids is dominated by that of graphene with a negligible effect from the dark current in HgTe QDs and can be optimized to its intrinsic limit by removing charge doping of adsorbed polar molecules on graphene. Furthermore, the R* is proportional to the photoconductive gain enabled by the strong quantum confinement in QDs and Gr. Achieving high gain in the MWIR spectrum, however, is challenging and requires elimination of charge traps primarily from the surface states of the narrow-bandgap semiconductor HgTe QDs. Using grain-rotation-induced grain-coalescence growth of single-layer and core/shell HgTe QDs, we show the that HgTe QDs surface states caused by Te deficiency can be dramatically suppressed, resulting in high gain up to 4.0 × 107 in the MWIR spectrum. The optimized noise and R* have led to high uncooled MWIR D* up to 2.4 × 1011 Jones, making nanohybrids promising to surpass the fundamental dark-current limit in conventional photodetectors. 

The Arctic Oscillation (AO) has been observed to undergo distinct decadal structural fluctuations that significantly influence regional weather and climate. Understanding the drivers and mechanisms behind the AO’s spatial nonstationarity is critical for improving climate predictions related to the AO. Wepresent evidence that the Atlantic Multidecadal Oscillation (AMO) plays a pivotal role in modulating AO’s Pacific center in recent decades. The poleward amplified cooling associated with negative AMO enhances the north-south temperature gradient and results the strengthened westerly winds and stratospheric polar vortex (SPV) responses, which reflects more planetary waves from the North Pacific to the North Atlantic. This enhances the atmospheric coupling between these regions and leads to amore pronounced Pacific center within theAOpattern.Numerical simulations fromECHAM5 and 35 CMIP6 models further corroborate the essential role of the AMO. These findings advance our understanding of the mechanisms driving the variability of the AO pattern. 

ABSTRACT Plant cytokinesis results in the formation of the cell plate by the phragmoplast which contains dynamic microtubules serving as the track for the delivery of cell wall builders included in Golgi vesicles. During the centrifugal process of cell plate assembly, new microtubules are assembled and bundled at the leading edge to prepare for vesicle transport while older microtubules are disassembled at the lagging edge upon the completion of vesicle delivery. The turnover of phragmoplast microtubules in this process is thought to be regulated by phosphorylation of the key microtubule bundling factor MAP65. A recent study revealed a surprising role of theα‐Aurora kinase, which is typically known for its role in governing the formation of the bipolar spindle apparatus, in phosphorylating the primary microtubule bundler MAP65‐3 in Arabidopsis. This phosphorylation positively contributes to the expansion of the phragmoplast. The phragmoplast midzone is also the hub for other cytokinesis‐important kinases. It is intriguing how these kinases are targeted and how they may crosstalk with each other to orchestrate the expansion of the phragmoplast. 

In plant vegetative tissues, cell division employs a mitotic microtubule array called the preprophase band (PPB) that marks the cortical division site. This transient cytoskeletal array imprints the spatial information to be read by the cytokinetic phragmoplast at later stages of mitotic cell division. In Arabidopsis thaliana, we discovered that the PPB recruited the Myosin XI motor MYA1/Myo11F to the cortical division site, where it joined microtubule-associated proteins and motors to form a ring of prominent cytoskeletal assemblies that received the expanding phragmoplast. Such a myosin localization pattern at the cortical division site was dependent on the POK1/2 Kinesin-12 motors. This regulatory function of MYA1/Myo11F in phragmoplast guidance was dependent on intact actin filaments. The discovery of these cytoskeletal motor assemblies pinpoints a mechanism underlying how two dynamic cytoskeletal networks work in concert to govern PPB-dependent division plane orientation in flowering plants. 

Single-atom catalysts have the advantage of high chemical efficiency, which requires atomic-scale control during catalyst formation. In order to address this challenge, this work explores the synthesis of single-atom platinum (SA-Pt) catalysts using atomic-layer deposition (ALD) on vertical graphene (VG), in which a large number of graphene edges serve as energetically favorable nucleation sites for SA-Pt, as predicted by density functional theory calculations. Interestingly, SA-Pt has been achieved on VGs at low ALD cycle numbers of up to 60. With a further increase in the number of ALD cycles, an increasing number of Pt clusters with diameters <2 nm and Pt nanoparticles (NPs) with diameters >2 nm become dominant (nano-Pt @VG). This is in contrast to the observation of predominantly nano-Pt on other carbon nanostructures, such as carbon nanotubes and monolayer graphene, under the same ALD growth conditions, indicating that the edge states on VG indeed play a critical role in facilitating the formation of SA-Pt. Profound differences are revealed in a comparative study on H2 sensing. SA-Pt exhibits both a higher sensitivity and faster response than its nano-Pt counterpart by more than an order of magnitude, illustrating the high catalytic efficiency of SAPt and its potential for gas sensing and a variety of other catalytic applications.