437 research outputs found
The Ecm11-Gmc2 complex promotes synaptonemal complex formation through assembly of transverse filaments in budding yeast
During meiosis, homologous chromosomes pair at close proximity to form the synaptonemal complex (SC). This association is mediated by transverse filament proteins that hold the axes of homologous chromosomes together along their entire length. Transverse filament proteins are highly aggregative and can form an aberrant aggregate called the polycomplex that is unassociated with chromosomes. Here, we show that the Ecm11-Gmc2 complex is a novel SC component, functioning to facilitate assembly of the yeast transverse filament protein, Zip1. Ecm11 and Gmc2 initially localize to the synapsis initiation sites, then throughout the synapsed regions of paired homologous chromosomes. The absence of either Ecm11 or Gmc2 substantially compromises the chromosomal assembly of Zip1 as well as polycomplex formation, indicating that the complex is required for extensive Zip1 polymerization. We also show that Ecm11 is SUMOylated in a Gmc2-dependent manner. Remarkably, in the unSUMOylatable ecm11 mutant, assembly of chromosomal Zip1 remained compromised while polycomplex formation became frequent. We propose that the Ecm11-Gmc2 complex facilitates the assembly of Zip1 and that SUMOylation of Ecm11 is critical for ensuring chromosomal assembly of Zip1, thus suppressing polycomplex formation
Traial on a ToF Measurement of Gamma-rays and Neutrons by a Diamond Radiation Detector with Fast Time Response
Direct and indirect control of the initiation of meiotic recombination by DNA damage checkpoint mechanisms in budding yeast
Meiotic recombination plays an essential role in the proper segregation of chromosomes at meiosis I in many sexually reproducing organisms. Meiotic recombination is initiated by the scheduled formation of genome-wide DNA double-strand breaks (DSBs). The timing of DSB formation is strictly controlled because unscheduled DSB formation is detrimental to genome integrity. Here, we investigated the role of DNA damage checkpoint mechanisms in the control of meiotic DSB formation using budding yeast. By using recombination defective mutants in which meiotic DSBs are not repaired, the effect of DNA damage checkpoint mutations on DSB formation was evaluated. The Tel1 (ATM) pathway mainly responds to unresected DSB ends, thus the sae2 mutant background in which DSB ends remain intact was employed. On the other hand, the Mec1 (ATR) pathway is primarily used when DSB ends are resected, thus the rad51 dmc1 double mutant background was employed in which highly resected DSBs accumulate. In order to separate the effect caused by unscheduled cell cycle progression, which is often associated with DNA damage checkpoint defects, we also employed the ndt80 mutation which permanently arrests the meiotic cell cycle at prophase I. In the absence of Tel1, DSB formation was reduced in larger chromosomes (IV, VII, II and XI) whereas no significant reduction was found in smaller chromosomes (III and VI). On the other hand, the absence of Rad17 (a critical component of the ATR pathway) lead to an increase in DSB formation (chromosomes VII and II were tested). We propose that, within prophase I, the Tel1 pathway facilitates DSB formation, especially in bigger chromosomes, while the Mec1 pathway negatively regulates DSB formation. We also identified prophase I exit, which is under the control of the DNA damage checkpoint machinery, to be a critical event associated with down-regulating meiotic DSB formation
Transport and Magnetic Studies on the Spin State Transition of Pr1-xCaxCoO3 up to High Pressure
Transport and magnetic measurements and structural and NMR studies have been
carried out on (Pr1-yR'y)1-xAxCoO3 {R'=(rare earth elements and Y); A=(Ca, Ba
and Sr)} at ambient pressure or under high pressure. The system exhibits a
phase transition from a nearly metallic to an insulating state with decreasing
temperature T, where the low spin (LS) state of Co3+ is suddenly stabilized.
For y=0, we have constructed a T-x phase diagram at various values of the
external pressure p. It shows that the (T, x) region of the low temperature
phase, which is confined to a very narrow region around x=0.5 at ambient
pressure, expands as p increases, suggesting that the transition is not due to
an order-disorder type one. For the occurrence of the transition, both the Pr
and Ca atoms seem to be necessary. The intimate relationship between the local
structure around the Co ions and the electronic (or spin) state of Co3+ ions is
discussed: For the smaller unit cell volume or the smaller volume of the CoO6
octahedra and for the larger tilting angle of the octahedra, the temperature of
the transition becomes higher. The role of the carriers introduced by the
doping of the A atoms, is also discussed. By analyzing the data of 59Co-NMR
spectra and magnetic susceptibilities of Pr1-xCaxCoO3 the energy separations
among the different spin states of Co3+ and Co4+ are roughly estimated.Comment: 15 pages, 15 figures, 2 tables, submitted to J. Phys. Soc. Jp
Trial of Fast Neutral Particles and Neutron Measurement by a Synthetic Diamond Radiation Detector
Traial on a ToF Measurement of Gamma-rays and Neutrons by a Diamond Radiation Detector with Fast Time Response
Transport and Magnetic Properties of R1-xAxCoO3 (R=La, Pr and Nd; A=Ba, Sr and Ca)
Transport and magnetic measurements have been carried out on perovskite
Co-oxides R1-xAxCoO3 (R=La, Pr, and Nd; A=Ba, Sr and Ca; 0<x<0.5: All sets of
the R and A species except Nd1-xBaxCoO3 have been studied.). With increasing
the Sr- or Ba-concentration x, the system becomes metallic ferromagnet with
rather large magnetic moments. For R=Pr and Nd and A=Ca, the system approaches
the metal- insulator phase boundary but does not become metallic. The magnetic
moments of the Ca-doped systems measured with the magnetic field H=0.1 T are
much smaller than those of the Ba- and Sr-doped systems. The thermoelectric
powers of the Ba- and Sr-doped systems decrease from large positive values of
lightly doped samples to negative ones with increasing doping level, while
those of Ca-doped systems remain positive. These results can be understood by
considering the relationship between the average ionic radius of R1-xAx and the
energy difference between the low spin and intermediate spin states. We have
found the resistivity-anomaly in the measurements of Pr1-xCaxCoO3 under
pressure in the wide region of x, which indicates the existence of a phase
transition different from the one reported in the very restricted region of
x~0.5 at ambient pressure [Tsubouchi et al. Phys. Rev. B 66 (2002) 052418.]. No
indication of this kind of transition has been observed in other species of R.Comment: 9 pages, 8 figures. J. Phys. Soc. Jpn. 72 (2003) No.
Evidence that MEK1 positively promotes interhomologue double-strand break repair
During meiosis there is an imperative to create sufficient crossovers for homologue segregation. This can be achieved during repair of programmed DNA double-strand breaks (DSBs), which are biased towards using a homologue rather than sister chromatid as a repair template. Various proteins contribute to this bias, one of which is a meiosis specific kinase Mek1. It has been proposed that Mek1 establishes the bias by creating a barrier to sister chromatid repair, as distinct from enforcing strand invasion with the homologue. We looked for evidence that Mek1 positively stimulates strand invasion of the homologue. This was done by analysing repair of DSBs induced by the VMA1-derived endonuclease (VDE) and flanked by directly repeated sequences that can be used for intrachromatid single-strand annealing (SSA). SSA competes with interhomologue strand invasion significantly more successfully when Mek1 function is lost. We suggest the increase in intrachromosomal SSA reflects an opportunistic default repair pathway due to loss of a MEK1 stimulated bias for strand invasion of the homologous chromosome. Making use of an inhibitor sensitive mek1-as1 allele, we found that Mek1 function influences the repair pathway throughout the first4–5 h of meiosis. Perhaps reflecting a particular need to create bias for successful interhomologue events before chromosome pairing is complete
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