Condor-G: A Computation Management Agent for Multi-Institutional Grids

In recent years, there has been a dramatic increase in the number of available computing and storage resources. Yet few tools exist that allow these resources to be exploited effectively in an aggregated form. We present the Condor-G system, which leverages software from Globus and Condor to enable users to harness multi-domain resources as if they all belong to one personal domain. We describe the structure of Condor-G and how it handles job management, resource selection, security, and fault tolerance. We also present results from application experiments with the Condor-G system. We assert that Condor-G can serve as a general-purpose interface to Grid resources, for use by both end users and higher-level program development tools.     

A System for Distributed Storage and Analysis of Genome Information

A distributed computing system is developed to search and analyze genetic databases using parallel computing technologies. Queries are processed by a local network PC cluster. A universal task and data exchange format is developed for effective query processing. A multilevel hierarchic task batching procedure is elaborated to generate multiple subtasks and distribute them over cluster units under dynamic priority levels and with dynamic distribution of replicated source data subbases. Primary source data preparation and generation of annotation word indices are used to significantly reduce query processing time.     

Workload characterization in a high-energy data grid and impact on resource management

The analysis of data usage in a large set of real traces from a high-energy physics collaboration revealed the existence of an emergent grouping of files that we coined “filecules”. This paper presents the benefits of using this file grouping for prestaging data and compares it with previously proposed file grouping techniques along a range of performance metrics. Our experiments with real workloads demonstrate that filecule grouping is a reliable and useful abstraction for data management in science Grids; that preserving time locality for data prestaging is highly recommended; that job reordering with respect to data availability has significant impact on throughput; and finally, that a relatively short history of traces is a good predictor for filecule grouping. Our experimental results provide lessons for workload modeling and suggest design guidelines for data management in data-intensive resource-sharing environments.

真核细胞染色体DNA复制起始及复制叉稳定性维持的机制

在真核生物中,DNA复制在染色体上特定的多位点起始．当细胞处在晚M及G1期,多个复制起始蛋白依次结合到DNA复制源,组装形成复制前复合体．pre．RC在Gl-S的转折期得到激活,随后,多个直接参与DNA复制又形成的蛋白结合到DNA复制源,启动DNA的复制,形成两个双向的DNA复制又．在染色体上,移动的DNA复制又经常会碰到复制障碍（二级DNA结构、一些蛋白的结合位点、损伤的碱基等）而暂停下来,此时,需要细胞周期检验点的调控来稳定复制叉,否则,会导致复制又垮塌及基因组不稳定．本文就真核细胞染色体DNA复制起始的机制,以及复制又稳定性的维持机制进行简要综述．     

Distributed File System Virtualization Techniques Supporting On-Demand Virtual Machine Environments for Grid Computing

This paper presents a data management solution which allows fast Virtual Machine (VM) instantiation and efficient run-time execution to support VMs as execution environments in Grid computing. It is based on novel distributed file system virtualization techniques and is unique in that: (1) it provides on-demand cross-domain access to VM state for unmodified VM monitors; (2) it enables private file system channels for VM instantiation by secure tunneling and session-key based authentication; (3) it supports user-level and write-back disk caches, per-application caching policies and middleware-driven consistency models; and (4) it leverages application-specific meta-data associated with files to expedite data transfers. The paper reports on its performance in wide-area setups using VMware-based VMs. Results show that the solution delivers performance over 30% better than native NFS and with warm caches it can bring the application-perceived overheads below 10% compared to a local-disk setup. The solution also allows a VM with 1.6 GB virtual disk and 320 MB virtual memory to be cloned within 160 seconds for the first clone and within 25 seconds for subsequent clones. Ming Zhao is a PhD candidate in the department of Electrical and Computer Engineering and a member of the Advance Computing and Information Systems Laboratory, at University of Florida. He received the degrees of BE and ME from Tsinghua University. His research interests are in the areas of computer architecture, operating systems and distributed computing. Jian Zhang is a PhD student in the Department of Electrical and Computer Engineering at University of Florida and a member of the Advance Computing and Information Systems Laboratory (ACIS). Her research interest is in virtual machines and Grid computing. She is a member of the IEEE and the ACM. Renato J. Figueiredo received the B.S. and M.S. degrees in Electrical Engineering from the Universidade de Campinas in 1994 and 1995, respectively, and the Ph.D. degree in Electrical and Computer Engineering from Purdue University in 2001. From 2001 until 2002 he was on the faculty of the School of Electrical and Computer Engineering of Northwestern University at Evanston, Illinois. In 2002 he joined the Department of Electrical and Computer Engineering of the University of Florida as an Assistant Professor. His research interests are in the areas of computer architecture, operating systems, and distributed systems.     

细胞自噬与病毒复制

细胞自噬是真核生物中一种高度保守的细胞内容物降解过程,在维持细胞的内环境稳定中起着重要作用。同时,自噬参与固有免疫系统对病原微生物的识别,以帮助吞噬细胞进行有效的吞噬作用并清除细胞内外的病原体。而病毒,尤其是RNA病毒,具有快速进化以应对宿主细胞中的变化的能力,能通过利用或抑制宿主细胞的自噬作用来为自身的复制服务。因此,针对自噬途径的药物筛选和治疗策略越来越成为抗病毒研究的热点。     

有丝分裂期DNA合成（MiDAS）及其介导的端粒复制

DNA复制压力（replication stress，RS）是一个广泛定义DNA复制障碍的术语，通常是指那些能够扰乱复制进程，造成复制叉减慢或停滞的情况。复制压力的过度累积是肿瘤发生和基因组不稳定的主要驱动因素。细胞染色体在复制过程中会不断地遭受来自外源性或内源性复制压力，而端粒及常见脆性位点（common fragile sites，CFSs）是一类对复制压力高度敏感的区域，在复制压力较高的情况下，这些区域往往难以被完全复制。近年的研究发现，有丝分裂期DNA合成（mitotic DNA repair synthesis，MiDAS）区别于S期的复制，可以帮助难以复制的区域在进入有丝分裂期后仍然能够保证复制的进行，因此，MiDAS也被称为“复制的挽救机制”。由于端粒的维持依赖于端粒酶活性及端粒替代性延长机制（alternative lengthening of telomeres，ALT），而具有更多端粒脆性的ALT细胞中端粒-MiDAS表现出高度的活性，因此本文就MiDAS的发生机制及在不同端粒维持机制下难以复制的端粒如何应对复制压力在有丝分裂期完成DNA的合成进行综述。     

Programming the Grid: Distributed Software Components, P2P and Grid Web Services for Scientific Applications

Computational Grids [17,25] have become an important asset in large-scale scientific and engineering research. By providing a set of services that allow a widely distributed collection of resources to be tied together into a relatively seamless computing framework, teams of researchers can collaborate to solve problems that they could not have attempted before. Unfortunately the task of building Grid applications remains extremely difficult because there are few tools available to support developers. To build reliable and re-usable Grid applications, programmers must be equipped with a programming framework that hides the details of most Grid services and allows the developer a consistent, non-complex model in which applications can be composed from well tested, reliable sub-units. This paper describes experiences with using a software component framework for building Grid applications. The framework, which is based on the DOE Common Component Architecture (CCA) [1,2,3,8], allows individual components to export function/service interfaces that can be remotely invoked by other components. The framework also provides a simple messaging/event system for asynchronous notification between application components. The paper also describes how the emerging Web-services [52] model fits with a component-oriented application design philosophy. To illustrate the connection between Web services and Grid application programming we describe a simple design pattern for application factory services which can be used to simplify the task of building reliable Grid programs. Finally we address several issues of Grid programming that better understood from the perspective of Peer-to-Peer (P2P) systems. In particular we describe how models for collaboration and resource sharing fit well with many Grid application scenarios.     

除虫链霉菌复制起始区克隆和功能初步分析

真细菌在复制起始区附近的基因排布顺序相当保守。根据DnaA和DnaN的氨基酸保守序列及链霉菌对密码子的偏用性 ,设计简并引物 ,以除虫链霉菌基因组DNA为模板扩增出一条约 1.4kb的片段。序列分析表明该片段含有部分的dnaA及dnaN基因 ,并在这两个基因之间有一段非编码区 ,其上有 19个典型的DnaA盒 ,推测是除虫链霉菌的复制起始区 (oriC)。与其他链霉菌已知的oriC作比较后发现除虫链霉菌的DnaA盒在位置、方向及间隔区的长度上都高度保守 ,并归纳出其保守序列为 (T/C) (T/C) (G/A/C)TCCACA(有下划线的碱基在该位置出现频率较高 )。将这段oriC插入到仅能在大肠杆菌中复制的质粒pQC15 6中 ,重组质粒可以成功转化变铅青链霉菌ZX7。对oriC分段研究发现其 3′部分对质粒的稳定性及转化效率有促进作用。     

Replication patterns and cytopathology of cells infected with baculoviruses

Conclusion In vitro studies have contributed greatly to an understanding of viral cytopathology, molecular biology, and pathogenesis. A model of the role of baculoviruses in a host-parasite relationship is developing which reveals the virus as gaining control of many aspects of host cell biology including control of the cell replication machinery (apoptotic response, macromolecular synthesis), the cytoskeletal structure, the nuclear membrane and intranuclear architecture. Baculovirus replication is a collection of independent but inter-related processes which work within the framework of the host cell, with the in vivo goal of maximizing production of progeny virions. Further molecular dissection of baculovirus replication should yield insight into the processes and principles of viral and host regulatory systems, perhaps facilitating development of new generations of high efficiency sub-viral expression vector systems and the development of genetically improved strains of virus safe for field use in ecologically based pest management strategies.     

质粒的复制特性和整合后在发动大肠杆菌染色体复制中对recA基因的依赖性的研究

大肠杆菌的温度敏感的DNA复制发动突变型dnaA46在42℃中不能生长而形成菌落,质粒或噬菌体的整合使它能生长。前文[2]报道了F质粒整合后所发动的染色体复制依赖于recA基因。本文报道5种质粒和2种噬菌体整合后所发动的染色体复制对recA基因的依赖性的研究结果。实验结果说明,依赖与否和它们在游离状态中复制方向无关,从而否定了recA基因的作用是把质粒或噬菌体的游离状态的单向复制发动机构改变为整合状态的双向复制发动饥构这一假设。     

Replication dynamics in fission and budding yeasts through DNA polymerase tracking

The dynamics of eukaryotic DNA polymerases has been difficult to establish because of the difficulty of tracking them along the chromosomes during DNA replication. Recent work has addressed this problem in the yeasts Schizosaccharomyces pombe and Saccharomyces cerevisiae through the engineering of replicative polymerases to render them prone to incorporating ribonucleotides at high rates. Their use as tracers of the passage of each polymerase has provided a picture of unprecedented resolution of the organization of replicons and replication origins in the two yeasts and has uncovered important differences between them. Additional studies have found an overlapping distribution of DNA polymorphisms and the junctions of Okazaki fragments along mononucleosomal DNA. This sequence instability is caused by the premature release of polymerase δ and the retention of non proof‐read DNA tracts replicated by polymerase α. The possible implementation of these new experimental approaches in multicellular organisms opens the door to the analysis of replication dynamics under a broad range of genetic backgrounds and physiological or pathological conditions.     

Global computing for bioinformatics

Global computing, the collaboration of idle PCs via the Internet in a SETI@home style, emerges as a new way of massive parallel multiprocessing with potentially enormous CPU power. Its relations to the broader, fast-moving field of Grid computing are discussed without attempting a review of the latter. This review (i) includes a short table of milestones in global computing history, (ii) lists opportunities global computing offers for bioinformatics, (iii) describes the structure of problems well suited for such an approach, (iv) analyses the anatomy of successful projects and (v) points to existing software frameworks. Finally, an evaluation of the various costs shows that global computing indeed has merit, if the problem to be solved is already coded appropriately and a suitable global computing framework can be found. Then, either significant amounts of computing power can be recruited from the general public, or--if employed in an enterprise-wide Intranet for security reasons--idle desktop PCs can substitute for an expensive dedicated cluster.     

Replication timing and cell differentiation

Cell differentiation may depend in part upon a type of unbalanced growth in which several cell cycles occur with a reduced level of total protein synthesis. During this period the synthesis of the chromatin protein HMG-I/Y is reduced since its synthesis is correlated with that of total protein. The synthesis of histone H1 shows less reduction since its synthesis is entrained with that of DNA. This greater reduction of HMG-I/Y than of histone H1 is thought to delay or prevent replicon initiations within AT-enriched isochores. This shifts their time of replication from early to late S phase. This may restrict certain pathways of cell differentiation in multipotent progenitor cells and allow one particular type of differentiation.     

PRIMPOL-Mediated Adaptive Response Suppresses Replication Fork Reversal in BRCA-Deficient Cells

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The Drosophila Werner Exonuclease Participates in an Exonuclease-Independent Response to Replication Stress

Members of the RecQ family of helicases are known for their roles in DNA repair, replication, and recombination. Mutations in the human RecQ helicases, WRN and BLM, cause Werner and Bloom syndromes, which are diseases characterized by genome instability and an increased risk of cancer. While WRN contains both a helicase and an exonuclease domain, the Drosophila melanogaster homolog, WRNexo, contains only the exonuclease domain. Therefore the Drosophila model system provides a unique opportunity to study the exonuclease functions of WRN separate from the helicase. We created a null allele of WRNexo via imprecise P-element excision. The null WRNexo mutants are not sensitive to double-strand break-inducing reagents, suggesting that the exonuclease does not play a key role in homologous recombination-mediated repair of DSBs. However, WRNexo mutant embryos have a reduced hatching frequency and larvae are sensitive to the replication fork-stalling reagent, hydroxyurea (HU), suggesting that WRNexo is important in responding to replication stress. The role of WRNexo in the HU-induced stress response is independent of Rad51. Interestingly, the hatching defect and HU sensitivity of WRNexo mutants do not occur in flies containing an exonuclease-dead copy of WRNexo, suggesting that the role of WRNexo in replication is independent of exonuclease activity. Additionally, WRNexo and Blm mutants exhibit similar sensitivity to HU and synthetic lethality in combination with mutations in structure-selective endonucleases. We propose that WRNexo and BLM interact to promote fork reversal following replication fork stalling and in their absence regressed forks are restarted through a Rad51-mediated process.     

Replication stress impairs chromosome segregation and preimplantation development in human embryos

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