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1.
Principal components (PCs) were calculated based on gene frequencies of 130 alleles at 38 loci in Chinese populations, and geographic PC maps were constructed. The first PC map of the Han shows the genetic difference between Southern and Northern Mongoloids, while the second PC indicates the gene flow between Caucasoid and Mongoloids. The first PC map of the Chinese ethnic minorities is similar to that of the second PC map of the Han, while their second PC map is similar to the first PC map of the Han. When calculating PC with the gene frequency data from both the Han and ethnic minorities, the first and second PC maps most resemble those of the ethnic minorities alone. The third and fourth PC maps of Chinese populations may reflect historical events that allowed the expansion of the populations in the highly civilized regions. A clear-cut boundary between Southern and Northern Mongoloids in the synthetic map of the Chinese populations was observed in the zone of the Yangtze River. We suggest that the a 相似文献
2.
Genetic distances were calculated for Han subpopulations in different provinces, cities and au-tonomous regions and ethnic minorities in China by using gene frequency data of 38 loci, and genetic trees were con-structed. The results showed that, among both Han and ethnic minorities, there were two types, i.e. southern and northern Mongoloids, with Yangtze River as boundary. Therefore, both African origin theory and local origin theory about the modern man should answer the question; when did these two types separate and how did they develop. This paper also conclusively proved genetically that the Han subpopulations in different regions are genetically close to the lo-cal ethnic minorities, which indicates that much blood of ethnic minorities has mixed into Han, at the same time, some blood of Han also has mixed into the local ethnic minorities. 相似文献
3.
兴安盟3个民族10对性状的基因频率 总被引:24,自引:3,他引:24
调查了内蒙古兴安盟汉、蒙古、朝鲜族的10对遗传性状,并计算了各民族每一性状的基因频率,同时也进行了民族间基因频率的比较。比较结果显示:汉族-朝鲜族间差异较大,蒙古族-朝鲜族间次之,汉族-蒙古族间差异较小。
Abstract:Ten genetic traits were investigated in Han,Mongol and Chaoxian nationalities in Xing'an League of Inner Mongolia.The gene frequency of the traits was calculated in each nationality and compared between the nationalities.The result indicated that the difference of gene frequency between Han and Chaoxian nationalities was significant,followed by between Mongol and Chaoxian ones,whileit was relatively insignificant between Han and Mongol ones. 相似文献
4.
新疆四个民族八对遗传性状的基因频率 总被引:14,自引:1,他引:14
阿不都拉·巴克 依米提·热合曼 木合塔尔·阿不都克里木 哈斯亚提 吾甫尔·依明 阿帕尔·吾甫尔 阿帕尔·加帕尔 米娜瓦尔 吾期库阿依 拉孜古力 热孜亚Abdula Bakhy Imit Rahman Muhtar Abdukerim Hasiyat Gupur Imin Gapar Gupur Gapar Japar Munawar Uqkunay Razigul Raziya 《遗传》1997,19(5):27-29
在调查新疆维吾尔、哈萨克、柯尔克孜、塔吉克族8对遗传性状的基础上分别计算出8对遗传性状在上述4个民族中的基因频率, 并进行了4个民族之间基因频率的比较。比较结果表明:塔吉克与其他3个民族之间基因频率的差异显著,而哈族与柯族之间的差异不显著。
Abstract:Acoording to the investigation of eight pairs of genetic traits among four minorities in Xinjiang (Uygur,Kazak,Kirgiz and Tajik),the gene frequencies of these traits were respectively calculated and compared.The results indicated that the difference of gene frequencies between Tajik and other three populations significant,while it is insignificant between kazak and Kirgiz. 相似文献
5.
中国汉蒙两族人群MTHFR基因热敏感性多态性分布的比较 总被引:7,自引:0,他引:7
为比较中国蒙汉两族人群MTHFR基因第677位核苷酸多态性的分布情况,获得该位点多态性的群体遗传学数据,本研究应用PCR扩增技术, 其扩增产物用限制性核酸内切酶Hinf I消化后进行非变性聚丙烯酰胺凝胶电泳,分析蒙汉族人群中MTHFR基因第677位核苷酸基因型(野生型、杂合型和突变纯合型)的分布频率。结果表明,蒙族人群基因型构成以野生型为主,占45.6%,突变杂合型占39.2%,突变纯合型仅占15.2%,汉族人群基因型构成以突变杂合型为主,占55.7%,野生型仅占17.9%,突变纯合型占26.4%,明显高于蒙族人群。经χ2检验,两组基因型构成比具有显著性差异(P<0.001);蒙族人群MTHFR 677T等位基因频率为34.8%,经u检验显著低于汉族人群(54.2%)的频率。据此认为,中国蒙族人群MTHFR热敏感性基因突变频率显著低于汉族人群,提示该基因多态性分布在中国不同民族人群中存在差异。
Abstract:The purpose of this study is to compare the genetic polymorphism distribution of the 677th nucleotide of MTHFR between the Mongolian population and the Hans of China,and to obtain the population genetic data of this polymorphism.Using PCR-RFLP method,the authors analyzed the genotypes of the 677th nucleotide of MTHFR in Mongolians and Hans.Results show that in Mongolian population,the proportion of wild type is 45.6%,proportion of heterozygotes is 39.2% and that of homozygotes is 15.2%; While in Hans,proportions are wild type 17.9%,heterozygotes 55.7% and homozygotes 26.4%.The ratios of genotypes are significantly different between Mongolian and Han populations(χ2-test,P<0.001).The 677th allele frequency in Mongolians is 34.8%,lower than that in Hans(54.2%,u-test,P<0.001).This suggests that the mutant MTHFR gene frequency is significantly higher in the Han population than in the Mongolian population in China. 相似文献
6.
本文报道了广西侗族、瑶族、壮族和汉族共554例受检者的Hp表型分布和基因频率。经χ2检验,4个群体中Hp表型分布符合Hardy-Weinberg遗传平衡法则。比较4个群体间Hp基因频率,无显著性差异,但汉族Hp1-1表型频率(0.110)显著高于侗族(0.0156)。本研究检出2-1M、2-H、2-1Tran、1-H和2-1H aw等5种变异型。
Abstract:This article deals with the phenotypes and gene frequencies of haptoglobin from 554 subjects belonging to 4 different ethnics,Dong,Yao,Zhuang and Han in Guangxi.The distribution of Hp phenotype in 4 ethnic groups is in agreement with the Hardy-Weinberg law.The gene frequencies of haptoglobin were compared with each other and no evidence of difference among these 4 populations was found.The variants,including 2-1M,2-H,2-1Tran,1-H and 2-1Haw were discovered in the experiment. 相似文献
7.
云南澜沧拉祜族HLA-DRB1基因多态性研究 总被引:6,自引:0,他引:6
采用我们改进的高分辨率基于内含子的PCR-SBT分型方法,首次检测云南拉祜族HLA-DRB1基因多态性。在55例拉祜族个体中共检出16种HLA-DRB1等位基因,最常见的DRB1等位基因是HLA-DRB1*12021、09012、15011,基因频率分别为30.909%、15.455%、13.636%,共占拉祜族可检出等位基因的60%,其中DRB1*0413、11081、1312、1418、1504首次在我国人群中检出,并且在世界各地人群中也比较罕见。对拉祜族和世界各地人群的HLA-DRB1频率进行了比较,分析了HLA-DRB1等位基因在各人种中的分布特点,并用Neighbor-joining法进行了聚类分析。比较分析的结果显示拉祜族明显属于中国南方族群,未显示出其族源来自北方的痕迹。对此遗传数据和民族学、历史学研究的矛盾,做了初步的分析。
Abstract:The HLA-DRB1 gene polymorphism in Lahu ethnic of Yunnan,China was the first time investigated using high resolution PCR-SBT method,which is based on sequences of HLA-DRB1 Intron 1 and Intron 2 and with our improvement.From 55 individuals of Lahu ethnic 16 DRB1 alleles were detected.The three most common alleles were HLA-DRB1*12021(30.909%),09012(15.455%),15011(13.636%),and they covered 60% of the total alleles detected from Lahu ethnic.HLA-DRB1*1413,*11081,*1312,*1418,*1504 were the first time detected in the Chinese,and were very rare in worldwide ethnic groups.With comparison of HLA-DRB1 gene frequencies between various ethnic groups we analysized the characteristics of HLA-DRB1 gene distribution in worldwide populations,and constructed the phylogenetic tree by Neighbor-joining method and Nei measure of genetic distance.The result showed Lahu ethnic obviously belong to the Chinese South ethnic groups and can't trace its origin from northern groups with the HLA-DRB1 genetic data.The preliminary explanations about the contradiction were given in this paper. 相似文献
8.
山东胃癌高低发人群Lewis基因多态性分析 总被引:1,自引:1,他引:0
应用PCR产物直接测序的方法,检测山东省胃癌高发的临朐人群和低发的苍山人群中Lewis基因多态性T59G的分布,旨在探讨山东临朐和苍山地区胃癌发病率显著不同的内在原因,为阐明临朐地区胃癌高发的机制提供实验依据。结果表明,T59G突变个体在临朐和苍山人群中的分布频率分别为34.5%和31.6%,差别无统计学意义,P>0.05,OR为1.14 (95% CI,0.59~2.19)。提示就此点突变而言,临朐人群和苍山人群为同一人群,具有极其相似的遗传背景;T59G不能作为区分临朐和苍山人群的遗传标志,与这两个地区胃癌发病的区别没有相关性。
Abstract:To explore the cause leading to the difference in incidence of gastric cancer between Linqu and Cangshan populations,Shandong Province,and to provide evidence for the possible mechanism of high incidence of gastric cancer in Linqu County,the distribution of T59G mutation in Lewis gene was screened between Linqu and Cangshan populations by PCR-sequencing.The frequency of individuals with T59G mutation was 34.5% in Linqu population and 31.6% in Cangshan population,respectively,with no significant difference,P>0.05,and OR is 1.14 (95% CI,0.59~2.19).This suggests that Linqu and Cangshan populations may share the same genetic background.T59G mutation of Lewis gene could not be used as a genetic marker for Linqu and Cangshan populations and is not relevant to the difference in incidence of gastric cancer between them. 相似文献
9.
PCR-RFLP检测LDL受体基因TaqⅠ多态性位点的研究 总被引:2,自引:0,他引:2
应用聚合酶链反应(PCR)扩增人类LDL受体基因外显子4-内含子4-外显子5片段,PCR产物为1.55kb,DNA片段经序列鉴定后,进行TaqI酶切位点的RFLP分析。结果显示:中国汉族人群LDL受体基因中存在着TaqⅠ酶切位点多态性; 200个LDL受体等位基因中TaqⅠ酶切位点出现的频率为0.515,该点频率较为适中, 可作为中国汉族人群LDL受体基
因的遗传标志来进行家族性高胆固醇血症(FH)的基因诊断。所建立起的LDL受体基因TaqⅠ位点的PCR -RFLP方法具有快速、简便的特点,在FH的基因诊断上有应用价值。
Abstract:To develop rapid and sensitive technique for detectin the TaqI polymorphism at the human LDL receptor gene in Chinese,the exon4-intron4-exon5 of the human LDL receptor gene was amplified by polymerase chain reaction(PCR).The PCR products were directly analysed by restriction fragment length polymorphisms(RFLP).The results showed that the TaqI polymorphism is associated with the LDL receptor gene in Chinese of Han nationality;The frequency of T= allele (presence of TaqI cutting site)is 0.515 in 200 LDL receptor alleles.This technique may be used for rapid and sensitive screening of the LDL receptor gene for the TaqI polymorphism. 相似文献
10.
内蒙古5个民族12对性状的基因频率 总被引:32,自引:2,他引:30
报道了内蒙古地区鄂温克、鄂伦春、达斡尔、蒙古族和汉族12对遗传性状的基因频率,并进行民族间基因频率的比较。结果显示:内眦褶性状的民族间差异较大,叠舌性状次之,利手和鼻梁侧面观性状的民族间差异较小。
Abstract:The gene frequency of 12 characters was reported in Ewenki,Oroqen,Daur,Mongol and Han nationalities in Inner Mongolia,and compared among these nationalities.The result indicated that the difference of Mongoloid fold among nationalities was significant,followed by the Folding tongue,while the difference of Handedness and Nasal profile was relatively insignificant. 相似文献
11.
Defects in mitochondrial energy metabolism have been implicated in the pathology of several neurodegenerative disorders. In addition, the reactive metabolites generated from the metabolism and oxidation of the neurotransmitter dopamine (DA) are thought to contribute to the damage to neurons of the basal ganglia. We have previously demonstrated that infusions of the metabolic inhibitor malonate into the striata of mice or rats produce degeneration of DA nerve terminals. In the present studies, we demonstrate that an intrastriatal infusion of malonate induces a substantial increase in DA efflux in awake, behaving mice as measured by in vivo microdialysis. Furthermore, pretreatment of mice with tetrabenazine (TBZ) or the TBZ analogue Ro 4-1284 (Ro-4), compounds that reversibly inhibit the vesicular storage of DA, attenuates the malonate-induced DA efflux as well as the damage to DA nerve terminals. Consistent with these findings, the damage to both DA and GABA neurons in mesencephalic cultures by malonate exposure was attenuated by pretreatment with TBZ or Ro-4. Treatment with these compounds did not affect the formation of free radicals or the inhibition of oxidative phosphorylation resulting from malonate exposure alone. Our data suggest that DA plays an important role in the neurotoxicity produced by malonate. These findings provide direct evidence that inhibition of succinate dehydrogenase causes an increase in extracellular DA levels and indicate that bioenergetic defects may contribute to the pathogenesis of chronic neurodegenerative diseases through a mechanism involving DA. 相似文献
12.
2018年中国植物科学若干领域重要研究进展 总被引:1,自引:0,他引:1
2018年中国植物科学继续呈现快速发展的态势, 我国科学家在国际植物科学主流学术刊物发表论文数量大幅增加, 取得了多项具有重要影响的成果。调控植物生长-代谢平衡实现可持续农业发展入选2018年度中国科学十大进展; 中国被子植物区系进化历史研究入选2018年度中国生命科学十大进展。以水稻为代表的农作物和果蔬等经济作物研究在国际上已呈现出明显的优势, 若干领域已从“追赶”状态跨越到“领跑”地位。该文对2018年中国科学家在植物科学若干领域取得的重要研究成果进行了概括性评述, 旨在全面追踪和报道当前中国植物科学领域的发展前沿和热点, 展示中国科学家所取得的杰出成就。 相似文献
13.
2017年中国植物科学若干领域重要研究进展 总被引:1,自引:0,他引:1
2017年中国植物科学继续保持高速发展态势, 重大成果频出, 具体表现在中国植物学家在国际顶级学术期刊发表的文章数量平稳上升。中国植物科学领域的研究工作者成果精彩纷呈, 如新型广谱抗病机制的发现、水稻广谱抗病遗传基础及机制和疫霉菌诱发病害成灾机制研究等。2017年中国生命科学领域十大进展评选中, 有两项植物科学领域的研究成果入选。水稻生物学、进化与基因组学和激素生物学等领域学科发展突出。另外, 值得一提的是, 长期从事高等植物与代谢途径调控分子网络研究和水稻品种设计育种的李家洋院士的研究成果“水稻高产优质性状形成的分子机理及品种设计”荣获2017年国家自然科学一等奖。这一具有重大国际影响的开创性贡献标志着中国植物科学在该领域的国际科学前沿居于引领和卓越地位。该文对2017年中国本土科学家在植物科学若干领域取得的重要研究成果进行了系统梳理, 旨在全面追踪和报道当前中国植物科学领域发展的最新前沿动态, 与广大读者共同分享我国科学家所取得的辉煌成就。 相似文献
14.
葫芦科植物包括多种瓜类蔬菜,对其进行离体培养研究具有重要的理论和实践意义。综述了国内在葫芦科植物器官培养、体细胞胚胎发生、花药培养、原生质体培养和体细胞杂交及离体遗传转化等方面取得的研究进展,并对葫芦科植物离体培养、遗传转化与育种的前景作了展望。 相似文献
15.
Somatostatin (SST) peptide is a potent inhibitor of insulin secretion and its effect is mediated via somatostatin receptor 5 (SSTR5) in the endocrine pancreas. To investigate the consequences of gene ablation of SSTR5 in the mouse pancreas, we have generated a mouse model in which the SSTR5 gene was specifically knocked down in the pancreatic beta cells (betaSSTR5Kd) using the Cre-lox system. Immunohistochemistry analysis showed that SSTR5 gene expression was absent in beta cells at three months of age. At the time of gene ablation, betaSSTR5Kd mice demonstrated glucose intolerance with lack of insulin response and significantly reduced serum insulin levels. Insulin tolerance test demonstrated a significant increase of insulin clearance in vivo at the same age. In vitro studies demonstrated an absence of response to SST-28 stimulation in the betaSSTR5Kd mouse islet, which was associated with a significantly reduced SST expression level in betaSSTR5Kd mice pancreata. In addition, betaSSTR5Kd mice had significantly reduced serum glucose levels and increased serum insulin levels at 12 months of age. Glucose tolerance test at an older age also indicated a persistently higher insulin level in betaSSTR5Kd mice. Further studies of betaSSTR5Kd mice had revealed elevated serum C-peptide levels at both 3 and 12 months of age, suggesting that these mice are capable of producing and releasing insulin to the periphery. These results support the hypothesis that SSTR5 plays a pivotal role in the regulation of insulin secretion in the mouse pancreas. 相似文献
16.
2018年中国植物科学继续呈现快速发展的态势, 我国科学家在国际植物科学主流学术刊物发表论文数量大幅增加, 取得了多项具有重要影响的成果。调控植物生长-代谢平衡实现可持续农业发展入选2018年度中国科学十大进展; 中国被子植物区系进化历史研究入选2018年度中国生命科学十大进展。以水稻为代表的农作物和果蔬等经济作物研究在国际上已呈现出明显的优势, 若干领域已从“追赶”状态跨越到“领跑”地位。该文对2018年中国科学家在植物科学若干领域取得的重要研究成果进行了概括性评述, 旨在全面追踪和报道当前中国植物科学领域的发展前沿和热点, 展示中国科学家所取得的杰出成就。 相似文献
17.
18.
Abstract. Changes are described in aquatic vegetation in oligotrophic, groundwater-fed Rhine floodplain streams in Alsace (eastern France), resulting from disturbance. Disturbance factors include changes in nutrients, either permanent ones - effluent from a waste water treatment plant or trout hatcheries - or periodic ones: flooding. Regular inputs of high levels of phosphate and ammonia modified the macrophyte vegetation in these streams. The floristic composition, which was characteristic of oligotrophic waters upstream of the eutrophicated sector, changed to that of a eutrophic situation as originally found downstream. Periodic disturbance by floods which normally occur once a year, irregularly eutrophicates the small streams, causing the development of a mixture of eutrophic and oligotrophic species. Six macrophyte communities are distinguished, indicating different trophic levels. The aquatic vegetation is adapted to the variations of phosphate and ammonia levels. Hence, aquatic macrophytes can be used as bio-indicators of fluctuations in water nutrient levels in relation to the type of disturbance. 相似文献
19.
K. Akiyama T.L. Gluckman A. Terhakopian P.M. Jinadasa S. Narayan S. Singaswamy B. Massey III R.J. Bing 《Tissue & cell》1997,29(6):733-743
We report the appearance of apoptotic cells in experimental myocardial infarction (rabbit heart) in in situ and in vitro preparations. Apoptosis was recognized by intravital staining with Hoechst 33342 (Ho342), by nick-end labeling (TUNEL) and by DNA laddering. A steady rise in the relative number of apoptotic cardiomyocytes (apoptotic index) was noted in in situ preparations. Apoptosis was first noted 6 h after the onset of ischemia with its highest value occurring after 72 h. Apoptotic nuclei were absent in remote areas of the left and right ventricles. Apoptotic nuclei within the infarcted area showed diminished intensity of Ho342 fluorescence. Three days after ischemia, a border zone adjacent to the infarcted area consisting of apoptotic macrophages was recognized. A novel finding was the appearance of apoptotic cardiomyocytes in the isolated perfused ischemic heart. Occurring as early as 50 min after the onset of ischemia, a high apoptotic index was present adjacent to the ligature placed around the coronary artery. This observation provides the opportunity to selectively examine factors leading to apoptosis in the ischemic heart under controlled experimental conditions. 相似文献
20.
节肢动物门是动物界最大的门,占整个动物种数的80%,全世界约有120万现存种。节肢动物在生长发育过程中会感染多种微生物,这些微生物会与其形成协同进化和互利共生的关系。内共生细菌是一类广泛分布于节肢动物体内的共生微生物,能够进行垂直传播和水平传播,对宿主的生长发育、生殖代谢、适应性、免疫功能和进化等诸多方面均具有重要的作用。目前,随着现代分子生物学理论和技术的发展,节肢动物内共生细菌相关研究主要集中在对其宿主的生殖调控功能、与其宿主、宿主寄主植物以及其宿主体内微生物和宿主天敌间互作关系等方面。因此,利用内共生细菌对昆虫种群动态的生殖调控功能,阻断热带蚊虫带来的疾病或植物病害的传播并对宿主昆虫进行种群压制或种群替换,可达到防控害虫的目的。本文从节肢动物内共生细菌的传播方式、对其宿主生物学效应以及内共生细菌与其宿主、宿主寄主植物、宿主天敌和宿主体内微生物互作关系等多方面进行概述,并对内共生细菌今后研究方向进行展望,以期为生物进化、物种形成和种群压制提供参考。 相似文献