30 research outputs found

    Type I phosphatidylinositol 4-phosphate 5-kinase controls neutrophil polarity and directional movement

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    Directional cell movement in response to external chemical gradients requires establishment of front–rear asymmetry, which distinguishes an up-gradient protrusive leading edge, where Rac-induced F-actin polymerization takes place, and a down-gradient retractile tail (uropod in leukocytes), where RhoA-mediated actomyosin contraction occurs. The signals that govern this spatial and functional asymmetry are not entirely understood. We show that the human type I phosphatidylinositol 4-phosphate 5-kinase isoform ÎČ (PIPKIÎČ) has a role in organizing signaling at the cell rear. We found that PIPKIÎČ polarized at the uropod of neutrophil-differentiated HL60 cells. PIPKIÎČ localization was independent of its lipid kinase activity, but required the 83 C-terminal amino acids, which are not homologous to other PIPKI isoforms. The PIPKIÎČ C terminus interacted with EBP50 (4.1-ezrin-radixin-moesin (ERM)-binding phosphoprotein 50), which enabled further interactions with ERM proteins and the Rho-GDP dissociation inhibitor (RhoGDI). Knockdown of PIPKIÎČ with siRNA inhibited cell polarization and impaired cell directionality during dHL60 chemotaxis, suggesting a role for PIPKIÎČ in these processes

    Lack of influence of the environment in the earliest stages of massive galaxy formation

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    We investigate how the environment affects the assembly history of massive galaxies. For that purpose, we make use of SHARDS and HST spectro-photometric data, whose depth, spectral resolution, and wavelength coverage allow to perform a detailed analysis of the stellar emission as well as obtaining unprecedentedly accurate photometric redshifts. This expedites a sufficiently accurate estimate of the local environment and a robust derivation of the star formation histories of a complete sample of 332 massive galaxies (>1010M⊙\mathrm{>10^{10}M_{\odot}}) at redshift 1≀z≀1.51\leq z \leq 1.5 in the GOODS-N field. We find that massive galaxies in this redshift range avoid the lowest density environments. Moreover, we observed that the oldest galaxies in our sample with with mass-weighted formation redshift z‟M−w≄2.5\mathrm{\overline{z}_{M-w} \geq 2.5}, avoid the highest density regions, preferring intermediate environments. Younger galaxies, including those with active star formation, tend to live in denser environments (ÎŁ=5.01.124.8×1010M⊙Mpc−2\Sigma = \mathrm{5.0_{1.1}^{24.8}\times 10^{10}M_{\odot}Mpc^{-2}}). This behavior could be expected if those massive galaxies starting their formation first would merge with neighbors and sweep their environment earlier. On the other hand, galaxies formed more recently (z‟M−w<2.5\overline{z}_{M-w} < 2.5) are accreted into large scale structures at later times and we are observing them before sweeping their environment or, alternatively, they are less likely to affect their environment. However, given that both number and mass surface densities of neighbor galaxies is relatively low for the oldest galaxies, our results reveal a very weak correlation between environment and the first formation stages of the earliest massive galaxies.Comment: Accepted for publication in MNRA

    Probing the Star Formation Main Sequence down to 10810^{8} M⊙_\odot at 1.0<z<3.01.0<z<3.0

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    We investigate the star formation main sequence (MS) (SFR-M⋆_{\star}) down to 108−9M⊙^{8-9}\mathrm{M}_\odot using a sample of 34,061 newly-discovered ultra-faint (27â‰Čiâ‰Č3027\lesssim i \lesssim 30 mag) galaxies at 1<z<31<z<3 detected in the GOODS-N field. Virtually these galaxies are not contained in previous public catalogs, effectively doubling the number of known sources in the field. The sample was constructed by stacking the optical broad-band observations taken by the HST/GOODS-CANDELS surveys as well as the 25 ultra-deep medium-band images gathered by the GTC/SHARDS project. Our sources are faint (average observed magnitudes ∌28.2\sim28.2 mag, ∌27.9\sim27.9 mag), blue (UV-slope ∌−1.9\sim-1.9), star-forming (rest-frame colors ∌0.10\sim0.10 mag, ∌0.17\sim0.17 mag) galaxies. These observational characteristics are identified with young (mass-weighted age ∌0.014\sim0.014 Gyr) stellar populations subject to low attenuations (∌0.30\sim0.30 mag). Our sample allows us to probe the MS down to 108.0 M⊙10^{8.0}\,\mathrm{M}_\odot at z=1z=1 and 108.5 M⊙10^{8.5}\,\mathrm{M}_\odot at z=3z=3, around 0.6 dex deeper than previous analysis. In the low-mass galaxy regime, we find an average value for the slope of 0.97 at 1<z<21<z<2 and 1.12 at 2<z<32<z<3. Nearly ∌\sim60% of our sample presents stellar masses in the range 106−810^{6-8} M⊙_\odot between 1<z<31<z<3. If the slope of the MS remained constant in this regime, the sources populating the low-mass tail of our sample would qualify as starburst galaxies.Comment: 34 pages, 16 figures, 9 tables. Accepted for publication to Ap

    Usefulness of a New Large Set of High Throughput EST-SNP Markers as a Tool for Olive Germplasm Collection Management

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    Germplasm collections are basic tools for conservation, characterization, and efficient use of olive genetic resources. The identification of the olive cultivars maintained in the collections is an important ongoing task which has been performed by both, morphological and molecular markers. In the present study, based on the sequencing results of previous genomic projects, a new set of 1,043 EST-SNP markers has been identified. In order to evaluate its discrimination capacity and utility in diversity studies, this set of markers was used in a representative number of accessions from 20 different olive growing countries and maintained at the World Olive Germplasm Collection of IFAPA Centre ‘Alameda del Obispo’ (Córdoba, Spain), one of the world’s largest olive germplasm bank. Thus, the cultivated material included: cultivars belonging to previously defined core collections by means of SSR markers and agronomical traits, well known homonymy cases, possible redundancies previously identified in the collection, and recently introduced accessions. Marker stability was tested in repeated analyses of a selected number of accessions, as well as in different trees and accessions belonging to the same cultivar. In addition, 15 genotypes from a cross ‘Picual’ × ‘Arbequina’ cultivars from the IFAPA olive breeding program and a set of 89 wild genotypes were also included in the study. Our results indicate that, despite their relatively wide variability, the new set of EST-SNPs displayed lower levels of genetic diversity than SSRs in the set of olive core collections tested. However, the EST-SNP markers displayed consistent and reliable results from different plant material sources and plant propagation events. The EST-SNPs revealed a clear cut off between inter- and intra-cultivar variation in olive. Besides, they were able to reliably discriminate among different accessions, to detect possible homonymy cases as well as efficiently ascertain the presence of redundant germplasm in the collection. Additionally, these markers were highly transferable to the wild genotypes. These results, together with the low genotyping error rates and the easy and fully automated procedure used to get the genotyping data, validate the new set of EST-SNPs as possible markers of choice for olive cultivar identification

    Probing the earliest phases in the formation of massive galaxies with simulated HST+JWST imaging data from Illustris

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    We use the Illustris-1 simulation to explore the capabilities of the Hubble\textit{Hubble} and James Webb Space Telescope\textit{James Webb Space Telescope} data to analyze the stellar populations in high-redshift galaxies, taking advantage of the combined depth, spatial resolution, and wavelength coverage. For that purpose, we use simulated broad-band ACS, WFC3 and NIRCam data and 2-dimensional stellar population synthesis (2D-SPS) to derive the integrated star formation history (SFH) of massive (M∗>1010 _{\ast}>10^{10}\,M⊙_{\odot}) simulated galaxies at 11011 110^{11}\,M⊙_{\odot} galaxy. In particular, we explore the potential of HST and JWST datasets reaching a depth similar to those of the CANDELS and ongoing CEERS observations, respectively, and concentrate on determining the capabilities of this dataset for characterizing the first episodes in the SFH of local M∗>1011 _{\ast}>10^{11}\,M⊙_{\odot} galaxies by studying their progenitors at z>1z>1. The 2D-SPS method presented in this paper has been calibrated to robustly recover the cosmic times when the first star formation episodes occurred in massive galaxies, i.e., the first stages in their integrated SFHs. In particular, we discuss the times when the first 1% to 50% of their total stellar mass formed in the simulation. We demonstrate that we can recover these ages with typical median systematic offset of less than 5% and scatter around 20%-30%. According to our measurements on Illustris data, we are able to recover that local M∗>1011 _{\ast}>10^{11}\,M⊙_{\odot} galaxies would have started their formation by z=16z=16, forming the first 5% of their stellar mass present at z∌1z \sim 1 by z=4.5z=4.5, 10% by z=3.7z=3.7, and 25% by z=2.7z=2.7.Comment: 28 pages, 13 figures, 4 tables. ApJ in press. Summary of changes from original submission: the major change is that we now include in Sec. 6 the comparison of the results obtained for our sample of massive 1 < z < 4 progenitors with those obtained by considering all massive galaxies at 1 < z < 4 in the simulated images. Several figures and sections have been update

    CEERS Key Paper V: A triality on the nature of HST-dark galaxies

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    The new capabilities that JWST offers in the near- and mid-infrared (IR) are used to investigate in unprecedented detail the nature of optical/near-IR faint, mid-IR bright sources, HST-dark galaxies among them. We gather JWST data from the CEERS survey in the EGS, jointly with HST data, and analyze spatially resolved optical-to-mid-IR spectral energy distributions (SEDs) to estimate both photometric redshifts in 2 dimensions and stellar populations properties in a pixel-by-pixel basis. We select 138 galaxies with F150W-F356W>1.5 mag, F356W<27.5 mag. The nature of these sources is threefold: (1) 71% are dusty star-forming galaxies at 2<z<6 with masses 9<log M/M_sun<11 and a variety of specific SFRs (100 Gyr^-1); (2) 18% are quiescent/dormant (i.e., subject to reignition and rejuvenation) galaxies at 3<z<5, masses log M/M_sun~10 and post-starburst stellar mass-weighted ages (0.5-1 Gyr); and (3) 11% are strong young starbursts with indications of high-EW emission lines (typically, [OIII]+Hbeta) at 6<z<7 and log M/M_sun~9.5. The sample is dominated by disk-like galaxies with a remarkable compactness for XELG-z6 (effective radii smaller than 0.4 kpc). Large attenuations in SFGs, 2<A(V)<5 mag, are found within 1.5 times the effective radius, approximately 2 kpc, while QGs present A(V)~0.2 mag. Our SED-fitting technique reproduces the expected dust emission luminosities of IR-bright and sub-millimeter galaxies. This study implies high levels of star formation activity between z~20 and z~10, where virtually 100% of our galaxies had already formed 10^8 M_sun of their stellar content, 60% of them had assembled 10^9 M_sun, and 10% up to 10^10 M_sun (in situ or ex situ). (abridged)Comment: Published in CEERS ApJL Focus Issue, ApJL 946, L1

    Adapting Agriculture to Climate Change: A Synopsis of Coordinated National Crop Wild Relative Seed Collecting Programs across Five Continents

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    The Adapting Agriculture to Climate Change Project set out to improve the diversity, quantity, and accessibility of germplasm collections of crop wild relatives (CWR). Between 2013 and 2018, partners in 25 countries, heirs to the globetrotting legacy of Nikolai Vavilov, undertook seed collecting expeditions targeting CWR of 28 crops of global significance for agriculture. Here, we describe the implementation of the 25 national collecting programs and present the key results. A total of 4587 unique seed samples from at least 355 CWR taxa were collected, conserved ex situ, safety duplicated in national and international genebanks, and made available through the Multilateral System (MLS) of the International Treaty on Plant Genetic Resources for Food and Agriculture (Plant Treaty). Collections of CWR were made for all 28 targeted crops. Potato and eggplant were the most collected genepools, although the greatest number of primary genepool collections were made for rice. Overall, alfalfa, Bambara groundnut, grass pea and wheat were the genepools for which targets were best achieved. Several of the newly collected samples have already been used in pre-breeding programs to adapt crops to future challenges.info:eu-repo/semantics/publishedVersio

    Identification and validation of novel EST-SSR markers in olives

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    ABSTRACT: The olive (Olea europaea L.) is a leading oil crop in the Mediterranean area. Limited information on the inheritance of agronomic significant traits hinders progress in olive breeding programs, which encourages the development of markers linked to the traits. In this study, we report on the development of 46 olive simple sequence repeat (SSR) markers, obtained from 577,025 expressed sequence tags (ESTs) in developing olive fruits generated in the framework of the Slovenian national olive transcriptome project. Sequences were de novo assembled into 98,924 unigenes, which were then used as a source for microsatellites searching. We identified 923 unigenes that contained 984 SSRs among which dinucleotide SSRs (36 %) were the most abundant, followed by tri- (33 %) and hexa- (21 %) nucleotides. Microsatellite repeat motif GA (37 %) was the most common among dinucleotides, while microsatellite repeat motif GAA was the most abundant trinucleotide SSR motif (16 %). Gene ontology annotations could be assigned to 27 % of the unigenes. A hundred and ten expressed sequence tag-derived-simple sequence repeats (EST-SSRs) with annotated genes were selected for primer designing and finally, 46 (42 %) polymorphic EST-SSRs were successfully amplified and used to validate genetic diversity among 24 olive varieties. The average number of alleles per locus, observed heterozygosity, expected heterozygosity, and polymorphic information content were 4.5, 0.649, 0.604 and 0.539, respectively. Twenty-seven EST-SSRs showed good diversity properties and were recommended for further olive genome investigation
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