太极拳干预社区中老年人亚健康状态的临床随机对照试验

目的:评价太极拳干预中老年亚健康的疗效。方法:采用随机单盲方法,将符合亚健康诊断标准的受试者100例,随机分为太极拳干预组和一般运动干预组。两组受试者分别进行每周三次,每次30min的太极拳锻炼和一般体育运动锻炼,疗程均为16周。临床疗效观察采用SF-36生命质量评分。结果:太极拳干预组生命质量干预前后评分差值与一般体育运动组比较显示:在总体健康和生命活力两个维度的差异有统计学意义。结论:太极拳较一般运动能更好地改善中老年亚健康人群生命质量。     

福建省青少年游泳运动员比赛表现的影响因素探析

采用文献资料法、问卷调查法、数理统计法,对影响福建省青少年游泳运动员比赛表现的影响因素进行研究。经过对34个因素进行因子分析,得出影响运动员比赛表现的影响因素的9个主因子。对9大因子进行分析得知,运动员比赛表现是个人技战术水平、心理能力、客观环境、人为因素、赛前准备、教练信任、对手作用、最佳体验与自我评价等多方面因素影响的结果,为我国游泳运动员训练和赛前控制比赛状态提供理论参考。     

基于人力资本视角下上海市高校体育教师培训体系的研究

运用人力资本理论,从改善上海市高校体育教师培训质量,优化体育教师人力资本等角度探讨了构建上海市高校体育教师培训体系的必要性,并设计出由培训需求评价、培训计划制定、培训过程实施与控制以及培训效果评估等各环节共同组成的科学培训体系。     

拓展训练在大学生情商教育中的价值探析

情商教育是高校教育中十分重要的环节,对大学生综合素质的培养有着重要意义。目前很多大学生情商较低,拓展训练作为高校情商教育的载体,能够提高大学生自信心、毅力、合作能力、人际交往能力和认知情绪能力。     

当代大学生体育消费特点及倾向性之研究

我国大学生体育消费特点呈现多样化的特点:1)体育消费动机多样化;2)实物型体育消费为主、参与型、观赏型体育消费为辅;3)体育消费能力存在较大的差异性。大学生未来的体育消费倾向呈现两大特点:1)体育消费意愿呈现增长态势;2)体育消费投入出现两极分化局面。根据我国大学生体育消费特点提出以下建议:1)加大终身体育教育理念的宣传;2)加大体育消费指导;3)加快学校体育社团建设。     

低盐刺激下副溶血弧菌基因转录表达分析

目的:应用全基因组DNA芯片技术分析低盐冷刺激作用下副溶血弧菌基因的转录表达变化.方法:分别采用"低盐持续刺激培养(continuous growth,CTG)"和"中间转入低盐环境培养(shift growth,STG)".CTG和STG下.分别采用含NaCl浓度为2%和0.66%的MV-5培养基孵育副溶血弧菌,收集菌体,提取RNA,应用全基因组DNA芯片分别比较两个不同的转录表达谱基因变化特点,分析其作用规律.同时,应用实时定量逆转录多聚酶联反应对芯片结果进行验证.结果:和对照组相比,STG实验中,共有205个基因的转录表达发生显著性变化,上调的基因占优势地位;CTG实验中,总计有298个基因的转录表达发生显著性变化,上、下涮的基因总体基本趋于平衡状态,没有明显差异.实时定量逆转录多聚酶联反应结果证实其和芯片数据结果有很强的相关性.结论:在低盐这一"胁迫环境"下,副溶血弧菌利用其存在的独特而精细的应对机制,能够顽强的生存下来并繁衍生殖,这一过程中,节能调节处于调控的核心地位.     

Mechanical unfolding intermediates in titin modules

The modular protein titin, which is responsible for the passive elasticity of muscle, is subjected to stretching forces. Previous work on the experimental elongation of single titin molecules has suggested that force causes consecutive unfolding of each domain in an all-or-none fashion. To avoid problems associated with the heterogeneity of the modular, naturally occurring titin, we engineered single proteins to have multiple copies of single immunoglobulin domains of human cardiac titin. Here we report the elongation of these molecules using the atomic force microscope. We find an abrupt extension of each domain by approximately 7 A before the first unfolding event. This fast initial extension before a full unfolding event produces a reversible 'unfolding intermediate' Steered molecular dynamics simulations show that the rupture of a pair of hydrogen bonds near the amino terminus of the protein domain causes an extension of about 6 A, which is in good agreement with our observations. Disruption of these hydrogen bonds by site-directed mutagenesis eliminates the unfolding intermediate. The unfolding intermediate extends titin domains by approximately 15% of their slack length, and is therefore likely to be an important previously unrecognized component of titin elasticity.     

Abundant gene conversion between arms of palindromes in human and ape Y chromosomes

Eight palindromes comprise one-quarter of the euchromatic DNA of the male-specific region of the human Y chromosome, the MSY. They contain many testis-specific genes and typically exhibit 99.97% intra-palindromic (arm-to-arm) sequence identity. This high degree of identity could be interpreted as evidence that the palindromes arose through duplication events that occurred about 100,000 years ago. Using comparative sequencing in great apes, we demonstrate here that at least six of these MSY palindromes predate the divergence of the human and chimpanzee lineages, which occurred about 5 million years ago. The arms of these palindromes must have subsequently engaged in gene conversion, driving the paired arms to evolve in concert. Indeed, analysis of MSY palindrome sequence variation in existing human populations provides evidence of recurrent arm-to-arm gene conversion in our species. We conclude that during recent evolution, an average of approximately 600 nucleotides per newborn male have undergone Y-Y gene conversion, which has had an important role in the evolution of multi-copy testis gene families in the MSY.     

High mutation rates have driven extensive structural polymorphism among human Y chromosomes

Although much structural polymorphism in the human genome has been catalogued, the kinetics of underlying change remain largely unexplored. Because human Y chromosomes are clonally inherited, it has been possible to capture their detailed relationships in a robust, worldwide genealogical tree. Examination of structural variation across this tree opens avenues for investigating rates of underlying mutations. We selected one Y chromosome from each of 47 branches of this tree and searched for large-scale variation. Four chromosomal regions showed extensive variation resulting from numerous large-scale mutations. Within the tree encompassed by the studied chromosomes, the distal-Yq heterochromatin changed length > or = 12 times, the TSPY gene array changed length > or = 23 times, the 3.6-Mb IR3/IR3 region changed orientation > or = 12 times and the AZFc region was rearranged > or = 20 times. After determining the total time spanned by all branches of this tree (approximately 1.3 million years or 52,000 generations), we converted these mutation counts to lower bounds on rates: > or = 2.3 x 10(-4), > or = 4.4 x 10(-4), > or = 2.3 x 10(-4) and > or = 3.8 x 10(-4) large-scale mutations per father-to-son Y transmission, respectively. Thus, high mutation rates have driven extensive structural polymorphism among human Y chromosomes. At the same time, we found limited variation in the copy number of Y-linked genes, which raises the possibility of selective constraints.