沙漠化对沙地土壤呼吸的影响及其对环境变化的响应

为了了解沙漠化过程中土壤呼吸速率变化及其对环境因素变化的响应,于2005年在科尔沁沙地研究了固定、半固定和流动沙地的土壤呼吸日变化和生长季动态及其与环境变化的关系,得出以下结论:(1)3种沙地土壤呼吸日变化在春季和秋季呈单峰曲线,夏季呈多峰曲线;(2)3种沙地土壤呼吸速率从春季到秋季的季节动态均呈双峰曲线,峰值分别出现在6月下旬和8月下旬;(3)固定和半固定沙地的土壤呼吸的日变化幅度明显大于流动沙地,季节变化幅度也是固定沙地半固定沙地流动沙地;(4)随着沙漠化的发展,土壤呼吸平均速率明显下降,生长季平均土壤呼吸速率从固定沙地的2.32μmolCO2/(m·2s)降为半固定的1.65μmolCO2/(m·2s)和流动沙地的1.06μmolCO2/(m·2s);(5)3种沙地土壤呼吸速率日变化均与土壤温度呈正相关,与空气湿度呈负相关,在季节尺度上3种沙地土壤呼吸速率与土壤温度、土壤水分和大气湿度均呈正相关,但只有固定沙地的相关性达到了显著水平;(6)沙漠化过程中,虽然土壤温度、土壤有机碳含量和植物根系碳含量都是导致沙地土壤呼吸发生改变的重要因子,但制约其变化的关键因子还是土壤水分和空气湿度。     

DNA导入和系选大豆品种及其亲本遗传关系的SSR标记分析

利用现有品种的变异进行系选并培育新品种是一种重要的育种方法。利用SSR标记, 对系选大豆（Glycine max）新品种和其亲本的遗传组成进行分析, 明确二者的遗传关系, 为大豆系选育种提供依据。使用48对SSR引物对22个大豆品种及其亲本进行分析, 结果表明, 由外源DNA导入育成的3个品种与其亲本的一致性为35.42%–95.83%, 虽然供体相同, 但由于导入的外源DNA不同, 故育成的品种间差异很大。另外19个系选品种与其亲本的一致性为27.08%–89.58%, 其中有6个品种与亲本间的差异小于30%。聚类分析发现, 所有参试品种分为东北春大豆及黄淮和南方大豆2类, 其中有8个品种不能与其亲本聚在一起, 说明系选品种并不完全是由于亲本通过突变获得。此外, 农艺性状与分子标记分析结果差异较大, 说明利用有限的农艺性状评价品种间的遗传关系存在一定的局限性。通过比较系选品种和亲本之间的保守位点发现, 特定等位变异出现次数≥7的位点有14个, 分布在11个连锁群, 其中有7个位点与产量和抗病性等重要农艺性状有关, 说明DNA导入和系选品种在选择变异性状的同时, 使一些与重要农艺性状有关的等位变异得到了保留。     

模拟硫酸型、硝酸型及其混合型酸雨对油菜生理特性、生长和产量的影响

为了了解我国酸雨污染由硫酸型向硫-硝酸复合型转变所引起的环境效应,以油菜(Brassicanapus)为供试材料,在大田试验条件下,系统研究了模拟硫酸型(SAR)、硝酸型(NAR)及其混合型(MAR)酸雨对农作物生理特性、生长和产量的影响。结果表明,3种酸雨胁迫均能抑制油菜生理、生长和产量形成,但不同类型的酸雨间的抑制效应存在差异。当pH≤4.1时,SAR、NAR、MAR能破坏油菜叶质膜系统、降低光合色素含量及光合速率,从而抑制作物的光合作用;当pH≤3.1时,油菜叶面积减小,叶受害百分率明显增加。pH=4.1可作为酸雨对油菜产量的影响阈值。在pH=7.0–1.5的酸度范围内,油菜叶片膜透性、丙二醛含量、叶受害百分率表现为NARMARSAR,光合速率、光合色素含量、叶面积及产量则表现出SARMARNAR的变化特征。当pH4.1时,3种酸雨处理间差异均不明显,pH≤3.1时,3种酸雨间的胁迫效应差异显著增加(p0.05),且酸度越强,差异越大,其变化趋势为NARMARSAR。说明NAR和MAR胁迫对油菜生理、生长及产量的抑制较大。     

Sequencing,annotation and comparative analysis of nine BACs of the giant panda(Ailuropoda melanoleuca)

A 10-fold BAC library for the giant panda was constructed and nine BACs were selected to generate finish sequences.These BACs could be used as a validation resource for the de novo assembly accuracy of the whole genome shotgun sequencing reads of the giant panda newly generated by Illumina GA sequencing technology.Complete Sanger sequencing,assembly,annotation and comparative analysis were carried out on the selected BACs of a joint length 878 kb.Homologue search and de novo prediction methods were used to ...     

向日葵胰蛋白酶抑制剂SFTI-1

向日葵胰蛋白酶抑制剂(sunflower trypsininhibitor-1,SFTI-1)是近来发现的Bowman-Birk抑制剂(Bowman-Birk inhibitor,BBI)家族的新成员。由14个氨基酸残基组成的SFTI-1是具有胰蛋白酶抑制活性的天然环肽。SFTI-1的天然环状结构使它成为药物研发中的重要前导化合物。本文综述了近年来SFTI-1在结构、功能、环化机制等方面的研究进展。     

交流外电场下映射神经元放电节律的分析

神经元不同的放电节律承载着不同的刺激信息。文章基于神经元映射模型,研究低频交流电场对神经元放电节律的影响。在外部刺激下映射模型表现出丰富的放电模式,包括周期簇放电、周期峰放电、交替放电和混沌放电。神经元对刺激频率和振幅的变化极为敏感,随着频率的增大,放电节律表现出从簇放电到峰放电和混沌放电的反向加周期分岔序列;在周期节律转迁过程中存在一种新的交替节律,其放电序列为两种周期放电模式的交替,峰峰间期序列具有整数倍特征。外电场的频率影响细胞内、外离子振荡周期,导致神经元放电与刺激信号同步,对放电节律的影响更为明显。研究结果揭示了交流外电场对神经元放电节律的作用规律,有助于探寻外电场对生物神经系统兴奋性的影响和神经系统疾病的致病机理。     

Identification of a novel gene (HSN2) causing hereditary sensory and autonomic neuropathy type II through the Study of Canadian Genetic Isolates

Hereditary sensory and autonomic neuropathy (HSAN) type II is an autosomal recessive disorder characterized by impairment of pain, temperature, and touch sensation owing to reduction or absence of peripheral sensory neurons. We identified two large pedigrees segregating the disorder in an isolated population living in Newfoundland and performed a 5-cM genome scan. Linkage analysis identified a locus mapping to 12p13.33 with a maximum LOD score of 8.4. Haplotype sharing defined a candidate interval of 1.06 Mb containing all or part of seven annotated genes, sequencing of which failed to detect causative mutations. Comparative genomics revealed a conserved ORF corresponding to a novel gene in which we found three different truncating mutations among five families including patients from rural Quebec and Nova Scotia. This gene, termed "HSN2," consists of a single exon located within intron 8 of the PRKWNK1 gene and is transcribed from the same strand. The HSN2 protein may play a role in the development and/or maintenance of peripheral sensory neurons or their supporting Schwann cells.     

Genetic analysis of a complex trait in the Utah Genetic Reference Project: a major locus for PTC taste ability on chromosome 7q and a secondary locus on chromosome 16p

The ability to taste phenylthiocarbamide (PTC) shows complex inheritance in humans. We obtained a quantitative measure of PTC tasting ability in 267 members of 26 large three-generation families that were part of a set of CEPH families that had been used for genetic mapping. Significant bimodality was found for the distribution of age and gender adjusted scores (P<0.001), with estimated means of 3.16 (SD=1.80) and 9.26 (SD=1.54). Using the extensive genotyping available in these families from the genetic mapping efforts, we performed a genome scan by using 1324 markers with an average spacing of 4 cM. Analyses were first carried out with a recessive genetic model that has traditionally been assumed for the trait, and a threshold score of 8.0 delineating tasters from non-tasters. In this qualitative analysis, the maximum genome-wide lod score was 4.74 at 246 cM on chromosome 7; 17 families showed segregation of the dichotomous PTC phenotype. No other lod scores were significant; the next highest score was on chromosome 10 (lod=1.64 at 85 cM), followed by chromosome 3 (lod=1.29 at 267 cM). Because PTC taste ability exhibited substantial quantitative variation, the quantitative trait was also analyzed by using a variance components approach in SOLAR. The maximum quantitative genome-wide lod score was 8.85 at 246 cM on chromosome 7. Evidence for other possible quantitative loci was found on chromosomes 1 (lod=2.31 at 344 cM) and 16 (lod=2.01 at 14 cM). A subsequent two-locus whole-genome scan conditional on the chromosome 7 quantitative trait locus identified the chromosome 16 locus (two-locus lod=3.33 at 14 cM).     

小麦对赤霉病抗性不同品种的SOD活性

本研究对9个赤霉病抗性不同小麦品种采用赤霉病菌分生孢子悬浮液以单花针注法进行了田间和温室抗病性鉴定;测定了各品种的胚性愈伤组织和盛花期麦穗分别经赤霉病菌毒素和分生孢子接种前后SOD活性的变化。结果表明,各品种SOD活性与其对赤霉病抗性呈极显著的正相关。接种后寄主的SOD活性均有提高,抗病品种比感病品种提高幅度大,且有新的同工酶带出现。抗病品种望水白比感病品种Alondra“S”多出两条SOD同工酶谱带。SOD在小麦抗赤霉病上可能起积极作用,其活性有可能作为鉴定小麦抗赤霉病的一种生理生化指标。     

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p

Autism is characterized by impairments in reciprocal communication and social interaction and by repetitive and stereotyped patterns of activities and interests. Evidence for a strong underlying genetic predisposition comes from twin and family studies, although susceptibility genes have not yet been identified. A whole-genome screen for linkage, using 83 sib pairs with autism, has been completed, and 119 markers have been genotyped in 13 candidate regions in a further 69 sib pairs. The addition of new families and markers provides further support for previous reports of linkages on chromosomes 7q and 16p. Two new regions of linkage have also been identified on chromosomes 2q and 17q. The most significant finding was a multipoint maximum LOD score (MLS) of 3.74 at marker D2S2188 on chromosome 2; this MLS increased to 4.80 when only sib pairs fulfilling strict diagnostic criteria were included. The susceptibility region on chromosome 7 was the next most significant, generating a multipoint MLS of 3.20 at marker D7S477. Chromosome 16 generated a multipoint MLS of 2.93 at D16S3102, whereas chromosome 17 generated a multipoint MLS of 2.34 at HTTINT2. With the addition of new families, there was no increased allele sharing at a number of other loci originally showing some evidence of linkage. These results support the continuing collection of multiplex sib-pair families to identify autism-susceptibility genes.