DNA primase acts as a molecular brake in DNA replication

A hallmark feature of DNA replication is the coordination between the continuous polymerization of nucleotides on the leading strand and the discontinuous synthesis of DNA on the lagging strand. This synchronization requires a precisely timed series of enzymatic steps that control the synthesis of an RNA primer, the recycling of the lagging-strand DNA polymerase, and the production of an Okazaki fragment. Primases synthesize RNA primers at a rate that is orders of magnitude lower than the rate of DNA synthesis by the DNA polymerases at the fork. Furthermore, the recycling of the lagging-strand DNA polymerase from a finished Okazaki fragment to a new primer is inherently slower than the rate of nucleotide polymerization. Different models have been put forward to explain how these slow enzymatic steps can take place at the lagging strand without losing coordination with the continuous and fast leading-strand synthesis. Nonetheless, a clear picture remains elusive. Here we use single-molecule techniques to study the kinetics of a multiprotein replication complex from bacteriophage T7 and to characterize the effect of primase activity on fork progression. We observe the synthesis of primers on the lagging strand to cause transient pausing of the highly processive leading-strand synthesis. In the presence of both leading- and lagging-strand synthesis, we observe the formation and release of a replication loop on the lagging strand. Before loop formation, the primase acts as a molecular brake and transiently halts progression of the replication fork. This observation suggests a mechanism that prevents leading-strand synthesis from outpacing lagging-strand synthesis during the slow enzymatic steps on the lagging strand.     

Rec8 phosphorylation and recombination promote the step-wise loss of cohesins in meiosis

During meiosis, cohesins--protein complexes that hold sister chromatids together--are lost from chromosomes in a step-wise manner. Loss of cohesins from chromosome arms is necessary for homologous chromosomes to segregate during meiosis I. Retention of cohesins around centromeres until meiosis II is required for the accurate segregation of sister chromatids. Here we show that phosphorylation of the cohesin subunit Rec8 contributes to step-wise cohesin removal. Our data further implicate two other key regulators of meiotic chromosome segregation, the cohesin protector Sgo1 and meiotic recombination in bringing about the step-wise loss of cohesins and thus the establishment of the meiotic chromosome segregation pattern. Understanding the interplay between these processes should provide insight into the events underlying meiotic chromosome mis-segregation, the leading cause of miscarriages and mental retardation in humans.     

Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin

Autosomal recessive juvenile parkinsonism (AR-JP) is an early-onset form of Parkinson's disease characterized by motor disturbances and dopaminergic neurodegeneration. To address its underlying molecular pathogenesis, we generated and characterized loss-of-function mutants of Drosophila PTEN-induced putative kinase 1 (PINK1), a novel AR-JP-linked gene. Here, we show that PINK1 mutants exhibit indirect flight muscle and dopaminergic neuronal degeneration accompanied by locomotive defects. Furthermore, transmission electron microscopy analysis and a rescue experiment with Drosophila Bcl-2 demonstrated that mitochondrial dysfunction accounts for the degenerative changes in all phenotypes of PINK1 mutants. Notably, we also found that PINK1 mutants share marked phenotypic similarities with parkin mutants. Transgenic expression of Parkin markedly ameliorated all PINK1 loss-of-function phenotypes, but not vice versa, suggesting that Parkin functions downstream of PINK1. Taken together, our genetic evidence clearly establishes that Parkin and PINK1 act in a common pathway in maintaining mitochondrial integrity and function in both muscles and dopaminergic neurons.     

Shallow water source localization using a mobile shor t horizontal array

This paper presents an approach to the challenging is- sue of passive source localization in shallow water using a mobile short horizontal linear array with length less than ten meters. The short array can be conveniently placed on autonomous underwa- ter vehicles and deployed for adaptive spatial sampling. However, the use of such small aperture passive sonar systems makes it difficult to acquire sufficient spatial gain for localizing long-range sources. To meet the requirement, a localization approach that employs matched-field based techniques that enable the short ho- rizontal linear array is used to passively localize acoustic sources in shallow water. Furthermore, the broadband processing and inter-position processing provide robustness against ocean en- vironmental mismatch and enhance the stability of the estimation process. The proposed approach＇s ability to localize acoustic sources in shallow water at different signal-to-noise ratios is examined through the synthetic test cases where the sources are located at the endfire and some other bearing of the mobile short horizontal linear array. The presented results demonstrate that the positional parameters of the estimated source build up over time as the array moves at a low speed along a straight line at a constant depth.     

基于两个L型阵列的远场多声源定位方法

针对传统方法不能准确地测量远场多声源位置的问题,提出了在近场和远场都能用的多声源3D定位新方法.该方法采用两个L型麦克风阵列,在每个阵列通过多声源的频率及到达角的联合估计求得信号源的夹角,基于每个信号源的夹角对估计多声源的位置.通过仿真实验验证了该方法在近场、远场都能准确地测量多声源位置,通过调节两个L型麦克风阵列之间的距离能得到误差在5%以下的声源定位精度.     

Polymer Materials for Fuel Cell Membranes ：Sulfonated Poly（ether sulfone） for Universal Fuel Cell Operations

Polymer electrolyte fuel cells （PEFCs） have been spotlighted because they are clean and highly efficient power generation system. Proton exchange membrane fuel cells （PEMFCs）, which use reformate gases or pure H2 for a fuel, have been employed for automotives and residential usages. Also, liquid-feed fuel cells such as direct methanol fuel cell （DMFC） and direct formic acid fuel cell （DFAFC） were studied for portable power generation.     

Basic amino-acid side chains regulate transmembrane integrin signalling

Side chains of Lys/Arg near transmembrane domain (TMD) membrane-water interfaces can 'snorkel', placing their positive charge near negatively charged phospholipid head groups; however, snorkelling's functional effects are obscure. Integrin β TMDs have such conserved basic amino acids. Here we use NMR spectroscopy to show that integrin β(3)(Lys?716) helps determine β(3) TMD topography. The α(ΙΙb)β(3) TMD structure indicates that precise β(3) TMD crossing angles enable the assembly of outer and inner membrane 'clasps' that hold the αβ TMD together to limit transmembrane signalling. Mutation of β(3)(Lys?716) caused dissociation of α(ΙΙb)β(3) TMDs and integrin activation. To confirm that altered topography of β(3)(Lys?716) mutants activated α(ΙΙb)β(3), we used directed evolution of β(3)(K716A) to identify substitutions restoring default state. Introduction of Pro(711) at the midpoint of β(3) TMD (A711P) increased α(ΙΙb)β(3) TMD association and inactivated integrin α(ΙΙb)β(3)(A711P,K716A). β(3)(Pro?711) introduced a TMD kink of 30?±?1° precisely at the border of the outer and inner membrane clasps, thereby decoupling the tilt between these segments. Thus, widely occurring snorkelling residues in TMDs can help maintain TMD topography and membrane-embedding, thereby regulating transmembrane signalling.