404 research outputs found
Unlocking a dark past.
A transcription factor called SALL4 could be the missing link between thalidomide and the limb defects caused by the drug
Important cardiac transcription factor genes are accompanied by bidirectional long non-coding RNAs
BackgroundHeart development is a relatively fragile process in which many transcription factor genes show dose-sensitive characteristics such as haploinsufficiency and lower penetrance. Despite efforts to unravel the genetic mechanism for overcoming the fragility under normal conditions, our understanding still remains in its infancy. Recent studies on the regulatory mechanisms governing gene expression in mammals have revealed that long non-coding RNAs (lncRNAs) are important modulators at the transcriptional and translational levels. Based on the hypothesis that lncRNAs also play important roles in mouse heart development, we attempted to comprehensively identify lncRNAs by comparing the embryonic and adult mouse heart and brain.ResultsWe have identified spliced lncRNAs that are expressed during development and found that lncRNAs that are expressed in the heart but not in the brain are located close to genes that are important for heart development. Furthermore, we found that many important cardiac transcription factor genes are located in close proximity to lncRNAs. Importantly, many of the lncRNAs are divergently transcribed from the promoter of these genes. Since the lncRNA divergently transcribed from Tbx5 is highly evolutionarily conserved, we focused on and analyzed the transcript. We found that this lncRNA exhibits a different expression pattern than that of Tbx5, and knockdown of this lncRNA leads to embryonic lethality.ConclusionThese results suggest that spliced lncRNAs, particularly bidirectional lncRNAs, are essential regulators of mouse heart development, potentially through the regulation of neighboring transcription factor genes
Reptilian Heart Development And The Molecular Basis Of Cardiac Chamber Evolution
The emergence of terrestrial life witnessed the need for more sophisticated circulatory systems. This has evolved in birds, mammals and crocodilians into complete septation of the heart into left and right sides, allowing separate pulmonary and systemic circulatory systems, a key requirement for the evolution of endothermy(1-3). However, the evolution of the amniote heart is poorly understood. Reptilian hearts have been the subject of debate in the context of the evolution of cardiac septation: do they possess a single ventricular chamber or two incompletely septated ventricles(4-7)? Here we examine heart development in the red-eared slider turtle, Trachemys scripta elegans (a chelonian), and the green anole, Anolis carolinensis (a squamate), focusing on gene expression in the developing ventricles. Both reptiles initially form a ventricular chamber that homogenously expresses the T-box transcription factor gene Tbx5. In contrast, in birds and mammals, Tbx5 is restricted to left ventricle precursors(8,9). In later stages, Tbx5 expression in the turtle (but not anole) heart is gradually restricted to a distinct left ventricle, forming a left-right gradient. This suggests that Tbx5 expression was refined during evolution to pattern the ventricles. In support of this hypothesis, we show that loss of Tbx5 in the mouse ventricle results in a single chamber lacking distinct identity, indicating a requirement for Tbx5 in septation. Importantly, misexpression of Tbx5 throughout the developing myocardium to mimic the reptilian expression pattern also results in a single mispatterned ventricular chamber lacking septation. Thus ventricular septation is established by a steep and correctly positioned Tbx5 gradient. Our findings provide a molecular mechanism for the evolution of the amniote ventricle, and support the concept that altered expression of developmental regulators is a key mechanism of vertebrate evolution
SALL4 Expression in Gonocytes and Spermatogonial Clones of Postnatal Mouse Testes
The spermatogenic lineage is established after birth when gonocytes migrate to the basement membrane of seminiferous tubules and give rise to spermatogonial stem cells (SSC). In adults, SSCs reside within the population of undifferentiated spermatogonia (Aundiff) that expands clonally from single cells (Asingle) to form pairs (Apaired) and chains of 4, 8 and 16 Aaligned spermatogonia. Although stem cell activity is thought to reside in the population of Asingle spermatogonia, new research suggests that clone size alone does not define the stem cell pool. The mechanisms that regulate self-renewal and differentiation fate decisions are poorly understood due to limited availability of experimental tools that distinguish the products of those fate decisions. The pluripotency factor SALL4 (sal-like protein 4) is implicated in stem cell maintenance and patterning in many organs during embryonic development, but expression becomes restricted to the gonads after birth. We analyzed the expression of SALL4 in the mouse testis during the first weeks after birth and in adult seminiferous tubules. In newborn mice, the isoform SALL4B is expressed in quiescent gonocytes at postnatal day 0 (PND0) and SALL4A is upregulated at PND7 when gonocytes have colonized the basement membrane and given rise to spermatogonia. During steady-state spermatogenesis in adult testes, SALL4 expression overlapped substantially with PLZF and LIN28 in Asingle, Apaired and Aaligned spermatogonia and therefore appears to be a marker of undifferentiated spermatogonia in mice. In contrast, co-expression of SALL4 with GFRα1 and cKIT identified distinct subpopulations of Aundiff in all clone sizes that might provide clues about SSC regulation. Collectively, these results indicate that 1) SALL4 isoforms are differentially expressed at the initiation of spermatogenesis, 2) SALL4 is expressed in undifferentiated spermatogonia in adult testes and 3) SALL4 co-staining with GFRα1 and cKIT reveals distinct subpopulations of Aundiff spermatogonia that merit further investigation. © 2013 Gassei, Orwig
Measurement of radon concentrations at Super-Kamiokande
Radioactivity from radon is a major background for observing solar neutrinos
at Super-Kamiokande. In this paper, we describe the measurement of radon
concentrations at Super-Kamiokande, the method of radon reduction, and the
radon monitoring system. The measurement shows that the current low-energy
event rate between 5.0 MeV and 6.5 MeV implies a radon concentration in the
Super-Kamiokande water of less than 1.4 mBq/m.Comment: 11 pages, 4 figure
Search for Supernova Relic Neutrinos at Super-Kamiokande
A search for the relic neutrinos from all past core-collapse supernovae was
conducted using 1496 days of data from the Super-Kamiokande detector. This
analysis looked for electron-type anti-neutrinos that had produced a positron
with an energy greater than 18 MeV. In the absence of a signal, 90% C.L. upper
limits on the total flux were set for several theoretical models; these limits
ranged from 20 to 130 nu_e bar cm^-2 s^-1. Additionally, an upper bound of 1.2
nu_e bar cm^-2 s^-1 was set for the supernova relic neutrino flux in the energy
region E_nu > 19.3 MeV.Comment: 4 pages, 2 figures. Submitted to Physical Review Letters. New version
includes corrections to Figure 1. Also, text has been shortened to conform
with the space limitations of PR
Observation of the east-west anisotropy of the atmospheric neutrino flux
The east-west anisotropy, caused by the deflection of primary cosmic rays in
the Earth's magnetic field, is observed for the first time in the flux of
atmospheric neutrinos. Using a 45 kt-year exposure of the
Super-Kamiokande detector, 552 e-like and 633 mu-like horizontally-going
events are selected in the momentum range between 400 and 3000 MeV/c.
The azimuthal distribution of e-like and mu-like events agrees with the
expectation from atmospheric neutrino flux calculations that account for the
geomagnetic field, verifying that the geomagnetic field effects in the
production of atmospheric neutrinos in the GeV energy range are well
understood.Comment: 8 pages,3 figures revtex, submitted to PR
The role of spalt proteins in development and disease
AbstractThe spalt proteins are encoded by a family of evolutionarily conserved genes found in species as diverse as Drosophila, C. elegans and vertebrates. In humans, mutations in some of these genes are associated with several congenital disorders which underscores the importance of spalt gene function in embryonic development. Recent studies have begun to cast light on the functions of this family of proteins with increasing understanding of the developmental processes regulated and the molecular mechanisms used. Here we review what is currently known about the role of spalt genes in vertebrate development and human disease
Tau Neutrinos Favored over Sterile Neutrinos in Atmospheric Muon Neutrino Oscillations
The previously published atmospheric neutrino data did not distinguish
whether muon neutrinos were oscillating into tau neutrinos or sterile
neutrinos, as both hypotheses fit the data. Using data recorded in 1100
live-days of the Super-Kamiokande detector, we use three complementary data
samples to study the difference in zenith angle distribution due to neutral
currents and matter effects. We find no evidence favoring sterile neutrinos,
and reject the hypothesis at the 99% confidence level. On the other hand, we
find that oscillation between muon and tau neutrinos suffices to explain all
the results in hand.Comment: 9 pages with 2 figures, submitted to PR
Constraints on Neutrino Oscillations Using 1258 Days of Super-Kamiokande Solar Neutrino Data
We report the result of a search for neutrino oscillations using precise
measurements of the recoil electron energy spectrum and zenith angle variations
of the solar neutrino flux from 1258 days of neutrino-electron scattering data
in Super-Kamiokande. The absence of significant zenith angle variation and
spectrum distortion places strong constraints on neutrino mixing and mass
difference in a flux-independent way. Using the Super-Kamiokande flux
measurement in addition, two allowed regions at large mixing are found.Comment: 6 pages, 4 figures, submitted to PR
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