1,852 research outputs found
Metal-Poor Stars Observed with the Magellan Telescope. III. New Extremely and Ultra Metal-Poor Stars from SDSS/SEGUE and Insights on the Formation of Ultra Metal-Poor Stars
We report the discovery of one extremely metal-poor (EMP; [Fe/H]<-3) and one
ultra metal-poor (UMP; [Fe/H]<-4) star selected from the SDSS/SEGUE survey.
These stars were identified as EMP candidates based on their medium-resolution
(R~2,000) spectra, and were followed-up with high-resolution (R~35,000)
spectroscopy with the Magellan-Clay Telescope. Their derived chemical
abundances exhibit good agreement with those of stars with similar
metallicities. We also provide new insights on the formation of the UMP stars,
based on comparison with a new set of theoretical models of supernovae
nucleosynthesis. The models were matched with 20 UMP stars found in the
literature, together with one of the program stars (SDSS J1204+1201), with
[Fe/H]=-4.34. From fitting their abundances, we find that the supernovae
progenitors, for stars where carbon and nitrogen are measured, had masses
ranging from 20.5 M_sun to 28 M_sun and explosion energies from 0.3 to
0.9x10^51 erg. These results are highly sensitive to the carbon and nitrogen
abundance determinations, which is one of the main drivers for future
high-resolution follow-up of UMP candidates. In addition, we are able to
reproduce the different CNO abundance patterns found in UMP stars with a single
progenitor type, by varying its mass and explosion energy.Comment: 15 pages, 12 figures; accepted for publication in Ap
Structural basis for the second step of group II intron splicing
The group II intron and the spliceosome share a common active site architecture and are thought to be evolutionarily related. Here we report the 3.7 Å crystal structure of a eukaryotic group II intron in the lariat-3′ exon form, immediately preceding the second step of splicing, analogous to the spliceosomal P complex. This structure reveals the location of the intact 3′ splice site within the catalytic core of the group II intron. The 3′-OH of the 5′ exon is positioned in close proximity to the 3′ splice site for nucleophilic attack and exon ligation. The active site undergoes conformational rearrangements with the catalytic triplex having dif- ferent configurations before and after the second step of splicing. We describe a complete model for the second step of group II intron splicing that incorporates a dynamic catalytic triplex being responsible for creating the binding pocket for 3′ splice site capture
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A gut-to-brain signal of fluid osmolarity controls thirst satiation.
Satiation is the process by which eating and drinking reduce appetite. For thirst, oropharyngeal cues have a critical role in driving satiation by reporting to the brain the volume of fluid that has been ingested1-12. By contrast, the mechanisms that relay the osmolarity of ingested fluids remain poorly understood. Here we show that the water and salt content of the gastrointestinal tract are precisely measured and then rapidly communicated to the brain to control drinking behaviour in mice. We demonstrate that this osmosensory signal is necessary and sufficient for satiation during normal drinking, involves the vagus nerve and is transmitted to key forebrain neurons that control thirst and vasopressin secretion. Using microendoscopic imaging, we show that individual neurons compute homeostatic need by integrating this gastrointestinal osmosensory information with oropharyngeal and blood-borne signals. These findings reveal how the fluid homeostasis system monitors the osmolarity of ingested fluids to dynamically control drinking behaviour
Variations in HIV Prevention Coverage in Subpopulations of Australian Gay and Bisexual Men, 2017–2021: Implications for Reducing Inequities in the Combination Prevention Era
Using repeated behavioural surveillance data collected from gay and bisexual men (GBM) across Australia, we assessed trends in HIV prevention coverage (the level of ‘safe sex’ achieved in the population by the use of effective prevention methods, including condoms, pre-exposure prophylaxis [PrEP] and having an undetectable viral load). We stratified these trends by age, country of birth/recency of arrival, sexual identity, and the proportion of gay residents in the participant’s suburb. Among 25,865 participants with casual male partners, HIV prevention coverage increased from 69.8% in 2017 to 75.2% in 2021, lower than the UNAIDS target of 95%. Higher levels of coverage were achieved among older GBM (≥ 45 years), non-recently-arrived migrants, and in suburbs with ≥ 10% gay residents. The lowest levels of prevention coverage (and highest levels of HIV risk) were recorded among younger GBM (< 25 years) and bisexual and other-identified participants. Younger, recently-arrived, and bisexual GBM were the most likely to use condoms, while PrEP use was concentrated among gay men, 25–44-year-olds, and in suburbs with more gay residents. The use of undetectable viral load was most common among participants aged ≥ 45 years. Our analysis shows that high HIV prevention coverage can be achieved through a mixture of condom use, PrEP use, and undetectable viral load, or by emphasising PrEP use. In the Australian context, younger, bisexual and other-identified GBM should be prioritised for enhanced access to effective HIV prevention methods. We encourage other jurisdictions to assess the level of coverage achieved by combination prevention, and variations in uptake
Adjusting Behavioural Surveillance and Assessing Disparities in the Impact of COVID-19 on Gay and Bisexual Men’s HIV-Related Behaviour in Australia
COVID-19 has disrupted sexual behaviour and access to health systems. We adapted regular HIV behavioural surveillance of gay and bisexual men (GBM) in Australia in response to COVID-19, assessed the impact on the profile of the sample, the participants’ HIV-related behaviour, and whether COVID-19 may have accentuated existing disparities in the Australian HIV epidemic. Data collected from five states during July 2017–June 2021 were included (N = 31,460). The emphasis on online recruitment after COVID-19 led to smaller sample sizes, greater geographic reach, and a higher proportion of bisexual-identifying participants. Most participants (88.1%) reported physical distancing and 52.1% had fewer sex partners due to COVID-19. In the COVID-19-affected rounds (July 2020–June 2021), the number of male partners, recent HIV testing and pre-exposure prophylaxis (PrEP) use all fell, and HIV risk among the smaller group of participants who reported casual sex increased. COVID-related changes were generally more pronounced among GBM aged under 25 years, participants from suburbs with fewer gay residents, and bisexual men. These groups should be prioritised when encouraging GBM to reengage with HIV testing services and effective prevention methods, like condoms and PrEP
Comparative Analysis of Tandem Repeats from Hundreds of Species Reveals Unique Insights into Centromere Evolution
Centromeres are essential for chromosome segregation, yet their DNA sequences
evolve rapidly. In most animals and plants that have been studied, centromeres
contain megabase-scale arrays of tandem repeats. Despite their importance, very
little is known about the degree to which centromere tandem repeats share
common properties between different species across different phyla. We used
bioinformatic methods to identify high-copy tandem repeats from 282 species
using publicly available genomic sequence and our own data. The assumption that
the most abundant tandem repeat is the centromere DNA was true for most species
whose centromeres have been previously characterized, suggesting this is a
general property of genomes. Our methods are compatible with all current
sequencing technologies. Long Pacific Biosciences sequence reads allowed us to
find tandem repeat monomers up to 1,419 bp. High-copy centromere tandem repeats
were found in almost all animal and plant genomes, but repeat monomers were
highly variable in sequence composition and in length. Furthermore,
phylogenetic analysis of sequence homology showed little evidence of sequence
conservation beyond ~50 million years of divergence. We find that despite an
overall lack of sequence conservation, centromere tandem repeats from diverse
species showed similar modes of evolution, including the appearance of higher
order repeat structures in which several polymorphic monomers make up a larger
repeating unit. While centromere position in most eukaryotes is epigenetically
determined, our results indicate that tandem repeats are highly prevalent at
centromeres of both animals and plants. This suggests a functional role for
such repeats, perhaps in promoting concerted evolution of centromere DNA across
chromosomes
OBSERVATIONAL CONSTRAINTS ON FIRST-STAR NUCLEOSYNTHESIS. II. SPECTROSCOPY OF AN ULTRA METAL-POOR CEMP-no STAR
We report on the first high-resolution spectroscopic analysis of HE 0020–1741, a bright (V = 12.9), ultra metal-poor ([Fe/H] = −4.1), carbon-enhanced ([C/Fe] = +1.7) star selected from the Hamburg/ESO Survey. This star exhibits low abundances of neutron-capture elements ([Ba/Fe] = −1.1) and an absolute carbon abundance A(C) = 6.1; based on either criterion, HE 0020–1741 is subclassified as a carbon-enhanced metal-poor star without enhancements in neutron-capture elements (CEMP-no). We show that the light-element abundance pattern of HE 0020–1741 is consistent with predicted yields from a massive (M = 21.5[subscript ⊙]), primordial-composition, supernova (SN) progenitor. We also compare the abundance patterns of other ultra metal-poor stars from the literature with available measures of C, N, Na, Mg, and Fe abundances with an extensive grid of SN models (covering the mass range 10-100M[subscript ⊙], in order to probe the nature of their likely stellar progenitors. Our results suggest that at least two classes of progenitors are required at [Fe/H] < -4.0, as the abundance patterns for more than half of the sample studied in this work (7 out of 12 stars) cannot be easily reproduced by the predicted yields.National Science Foundation (U.S.) (CAREER Grant AST-1255160
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