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牦牛乳酸脱氢酶-1两种遗传变异体的纯化及酶学特性比较 被引量:5
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作者 郑玉才 赵兴波 +6 位作者 周静 朴影 金素钰 贺庆华 洪键 李宁 吴常信 《中国农业科学》 CAS CSCD 北大核心 2009年第3期1047-1052,共6页
【目的】从乳酸脱氢酶(LDH)水平上探索牦牛(Bos grunniens)低氧适应性分子机制。【方法】利用聚丙烯酰胺凝胶电泳分析牦牛组织中LDH同工酶谱;用比色法测定牦牛、黄牛和水牛心脏、肝脏和肌肉组织中LDH总活力;采用染料亲和层析和DEAE-Seph... 【目的】从乳酸脱氢酶(LDH)水平上探索牦牛(Bos grunniens)低氧适应性分子机制。【方法】利用聚丙烯酰胺凝胶电泳分析牦牛组织中LDH同工酶谱;用比色法测定牦牛、黄牛和水牛心脏、肝脏和肌肉组织中LDH总活力;采用染料亲和层析和DEAE-Sephadex离子交换层析从牦牛心肌组织中纯化LDH1(由4个H亚基组成)的2种遗传变异体,进行酶学性质的比较。【结果】电泳方法检测发现牦牛LDH1存在2种遗传变异体,根据电泳迁移率分别命名为快型和慢型(LDH1-F和LDH1-S)。获得纯化的牦牛LDH1-F和LDH1-S,比活力分别为21.4U·mg-1蛋白和17.8U·mg-1蛋白,在SDS-PAGE和PAGE上均显示1条区带。2种变异体以NADH为底物的米氏常数(Km)值差异不大,均显著高于普通牛的LDH1;以丙酮酸钠为底物的Km值LDH1-F小于LDH1-S。试验进一步比较了携带不同LDH1变异体的牦牛心脏、肝脏和肌肉组织中LDH总活力和各种同工酶谱,未见显著差异,而牦牛心脏、肝脏和肌肉组织中LDH总活力显著或极显著低于黄牛和水牛。【结论】牦牛LDH12种遗传变异体的Km值存在差异,且Km(NADH)高于普通牛;牦牛心脏、肝脏和肌肉组织中LDH总活力低于普通牛。 展开更多
关键词 牦牛 乳酸脱氢酶 遗传变异体 低氧耐受 分子适应性
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用毛细管电泳检测牦牛、犏牛和藏黄牛乳中β-乳球蛋白的三种遗传变异体 被引量:1
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作者 任亮 黄林 +6 位作者 蒋忠荣 高杰 刘曦 卢帮敏 金素钰 林亚秋 郑玉才 《食品工业科技》 CAS CSCD 北大核心 2014年第5期137-140,共4页
利用毛细管电泳(CE)分离牛乳中β-乳球蛋白(β-Lg)的三种遗传变异体,为牛乳的质量监控提供方法。分别制备牦牛、犏牛和藏黄牛乳清,用聚丙烯酰胺凝胶电泳(PAGE)和CE分析乳清蛋白。结果表明,CE法与PAGE法都能有效分离β-Lg的三种遗传变异... 利用毛细管电泳(CE)分离牛乳中β-乳球蛋白(β-Lg)的三种遗传变异体,为牛乳的质量监控提供方法。分别制备牦牛、犏牛和藏黄牛乳清,用聚丙烯酰胺凝胶电泳(PAGE)和CE分析乳清蛋白。结果表明,CE法与PAGE法都能有效分离β-Lg的三种遗传变异体;在牦牛乳中加入不同比例的犏牛乳,用CE法可检测到的犏牛乳最低添加比例约为5%,线性关系好。另外,对藏黄牛杂合型β-Lg的两种遗传变异体分析显示,CE法比PAGE法能更准确对β-Lg A和β-Lg B的相对比例进行分析。本研究结果表明,CE方法能对乳中β-Lg的三种遗传变异体进行有效分离和定量分析,在牦牛乳的质量监控方面具有潜在的应用价值。 展开更多
关键词 毛细管电泳 牦牛 Β-乳球蛋白 遗传变异体
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西藏牦牛血清乳酸脱氢酶H亚基的遗传变异体 被引量:12
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作者 郑玉才 陈智华 《青海畜牧兽医杂志》 1997年第1期14-16,共3页
采用聚丙烯酰胺凝胶电泳分析西藏嘉黎和亚东地区85头牦牛血清乳酸脱氢酶(LDH)同工酶。结果显示,牦牛血清LDH同工酶具有LDH1~LDH5五种形式,LDH的H亚基存在A、B、C三种遗传变异体,C型遗传变异体平均占82... 采用聚丙烯酰胺凝胶电泳分析西藏嘉黎和亚东地区85头牦牛血清乳酸脱氢酶(LDH)同工酶。结果显示,牦牛血清LDH同工酶具有LDH1~LDH5五种形式,LDH的H亚基存在A、B、C三种遗传变异体,C型遗传变异体平均占82.35%。值得注意的是,嘉黎地区具有A或B型H亚基的牦牛血清中LDH2的相对活力显著低于具有C型H亚基的牦牛,其机制和意义有待进一步研究。 展开更多
关键词 牦牛 乳酸脱氢酶 遗传变异体
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牦牛β-酪蛋白A1、A2型遗传变异体的基因和蛋白质水平分析 被引量:5
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作者 罗卉卉 金素钰 +1 位作者 黄林 郑玉才 《黑龙江畜牧兽医》 CAS 北大核心 2020年第6期133-135,140,158,共5页
乳β-酪蛋白(β-CN)序列与其功能有关,β-CN的A2遗传变异体被认为更有利于人体健康。为了明确麦洼牦牛和九龙牦牛β-CN的遗传变异体,试验首先以60头牦牛的基因组DNA(提取于九龙牦牛20份肉样、麦洼牦牛20份肉样和20份乳样)为模板,用PCR... 乳β-酪蛋白(β-CN)序列与其功能有关,β-CN的A2遗传变异体被认为更有利于人体健康。为了明确麦洼牦牛和九龙牦牛β-CN的遗传变异体,试验首先以60头牦牛的基因组DNA(提取于九龙牦牛20份肉样、麦洼牦牛20份肉样和20份乳样)为模板,用PCR方法扩增β-CN编码基因CSN2的部分序列,用PCR-SSCP分析确定基因型;再用酸性尿素聚丙烯酰胺凝胶电泳直接分析了36头九龙牦牛乳的β-CN基因型。结果表明:建立的PCR-SSCP方法能准确地判定CSN2的3种基因型,即A1A1、A1A2和A2A2型。两个品种牦牛A2A2基因型频率均在0.900以上,A2等位基因占明显优势。36份九龙牦牛乳样共检测到A1和A2型两种遗传变异体,对应的基因型分别为A1A2(n=2)、A2A2(n=34),A2等位基因亦占绝对优势。基因水平和蛋白质水平上的分析均说明麦洼牦牛和九龙牦牛CSN2以A2A2基因型为主,乳中β-CN为A2型遗传变异体,牦牛乳属于优质的奶源。 展开更多
关键词 牦牛 A1型乳 A2型乳 遗传变异体 单链构象多态性
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p21活化激酶2基因变异体rs3662C>A与卒中风险和预后的关系及其对转录活性的影响
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作者 司斌 张舒媛 +2 位作者 杨云云 陈宇 张伟丽 《基础医学与临床》 2021年第4期472-478,共7页
目的探讨p21活化激酶2(PAK2)基因变异体rs3662C>A与卒中风险及预后的关系和机制。方法收集动脉粥样硬化性脑梗死患者733例、腔隙性脑梗死488例、脑出血435例和健康对照1727人的资料,利用logistic回归模型分析rs3662C>A与卒中风险... 目的探讨p21活化激酶2(PAK2)基因变异体rs3662C>A与卒中风险及预后的关系和机制。方法收集动脉粥样硬化性脑梗死患者733例、腔隙性脑梗死488例、脑出血435例和健康对照1727人的资料,利用logistic回归模型分析rs3662C>A与卒中风险的关系,Cox生存回归模型分析rs3662C>A与卒中预后的关系。利用荧光素酶报告基因实验分析rs3662C>A对PAK2转录活性的影响。结果与rs3662CC基因型比较,rs3662A与降低动脉粥样硬化性脑梗死的患病风险相关,比值比为0.67(95%CI:0.47~0.95,P<0.05;显性遗传模型),且主要在男性中相关。平均随访4.5年,携带rs3662A的动脉粥样硬化性脑梗死患者发生心脑血管事件和心血管病死亡的风险升高,风险比分别为1.84(95%CI:1.16~2.92,P<0.05)和2.06(95%CI:1.05~4.04,P<0.05)。rs3662C降低荧光素酶表达活性的79%(P<0.01)。结论PAK2基因rs3662A的携带者患动脉粥样硬化性脑梗死的风险低于rs3662CC携带者,但预后不良。rs3662C>A影响PAK2表达活性。 展开更多
关键词 p21活化激酶2(PAK2) 遗传变异体 易感性 卒中 预后
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《Nature》发布迄今最大规模人类遗传变异数据库
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《上海医药》 CAS 2020年第11期73-73,共1页
5月27日,国际期刊《Nature》及其子刊在线发表了基因组聚集数据库(gnomAD)团队的系列研究论文。据悉,这份汇集了逾14万人的公开目录是迄今为止最大规模的人体遗传变异体数据库,将有助于人们深入了解人类基因功能,增强对罕见和常见遗传... 5月27日,国际期刊《Nature》及其子刊在线发表了基因组聚集数据库(gnomAD)团队的系列研究论文。据悉,这份汇集了逾14万人的公开目录是迄今为止最大规模的人体遗传变异体数据库,将有助于人们深入了解人类基因功能,增强对罕见和常见遗传病的理解。gnomAD项目是一个大规模的人类遗传变异体数据库,通过各种大型人群测序项目汇集数据,来鉴定各种功能丧失型变异体。 展开更多
关键词 数据库 国际期刊 遗传变异体 遗传 功能丧失 基因功能
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牛乳酪蛋白遗传多态性研究 被引量:9
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作者 崔艳华 马莺 +1 位作者 何胜华 李海梅 《中国乳品工业》 CAS 北大核心 2010年第5期32-37,共6页
牛乳酪蛋白遗传多态性影响着牛乳的组成和干酪制作,同时是研究牛品种特性和系统进化的有用工具。就牛乳中酪蛋白的遗传多态性、乳酪蛋白遗传多态性的研究方法以及酪蛋白多态性与乳品质之间的相关性等进行综述,旨在阐述当前牛乳酪蛋白遗... 牛乳酪蛋白遗传多态性影响着牛乳的组成和干酪制作,同时是研究牛品种特性和系统进化的有用工具。就牛乳中酪蛋白的遗传多态性、乳酪蛋白遗传多态性的研究方法以及酪蛋白多态性与乳品质之间的相关性等进行综述,旨在阐述当前牛乳酪蛋白遗传多态性研究的现状,为今后该方向研究提供参考。 展开更多
关键词 酪蛋白 遗传多态性 遗传变异体
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牛乳清蛋白遗传多态性研究
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作者 曹喻 崔艳华 +2 位作者 曲晓军 董爱军 马莺 《中国乳品工业》 CAS 北大核心 2011年第5期43-46,64,共5页
就牛乳清蛋白遗传多态性及其研究方法以及乳清蛋白多样性与乳品质之间的相关性作以阐述,旨在揭示当前该方向研究现状,并为今后研究提供参考。
关键词 乳清蛋白 遗传多态性 遗传变异体
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能显示移植配型错误的遗传试验
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作者 袁波 《国外医学情报》 1992年第10期17-17,共1页
由于在移植配型时有错误,因而有多达四分之一的被移植肾对移植病人不是密切匹配的。这种错误配型可能解释移植病人的许多不能解释的肾功能衰竭。上述结论是由指导一项在欧洲和美国由4000多人参加研究的西德免疫学家Gerhard Opelz获得的... 由于在移植配型时有错误,因而有多达四分之一的被移植肾对移植病人不是密切匹配的。这种错误配型可能解释移植病人的许多不能解释的肾功能衰竭。上述结论是由指导一项在欧洲和美国由4000多人参加研究的西德免疫学家Gerhard Opelz获得的。Opelz及其研究小组用最近发明的一种以DNA为主的组织配型技术发现了移植配型的不符合性。 展开更多
关键词 移植配型 移植肾 肾移植 组织配型 遗传变异体 错误 试验组 免疫学家 完全匹配 符合性
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SSR Analysis of Three Species from Primary Parent and Their First Generation of Litopenaeus vannamei 被引量:2
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作者 栗志民 谢丽 +1 位作者 叶富良 陈国良 《Agricultural Science & Technology》 CAS 2010年第3期57-61,共5页
Genetic variations of three species from primary parent (OI Q,SIS Q,Kona Bay Q) and their first filial generation (OI Z,SIS Z,Kona Bay Z) of Litopenaeus vannamei were detected using microsatellite marker technique... Genetic variations of three species from primary parent (OI Q,SIS Q,Kona Bay Q) and their first filial generation (OI Z,SIS Z,Kona Bay Z) of Litopenaeus vannamei were detected using microsatellite marker technique.The amplified products of genomic DNA with 8 microsatellite makers indicated that 8 loci presents polymorphism,the number of total alleles were 28 in 6 species;the number of allele of every loci was 2 to 6;mean allele number (Na) was 3.5;expected heterozygosity value (He) were higher than observed heterozygosity value (Ho);mean polymorphism information content (PIC) ranged from 0.479 4 to 0.769 9,which showed these 8 loci posses relatively high information content.Through analysis of genetic structure in primary parent and their first filial,allele and effective allele number,observed heterozygosity and expected heterozygosity values and mean polymorphism information content (PIC) in filial generation were little lower than their primary parents.However,genetic diversity of filial generation is not influenced,and still maintains a good heritability. 展开更多
关键词 Litopenaeus vanname MICROSATELLITE Brood and F1 stocks Genetic variation
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Analysis of Genetic Variation and Population Structure of Starch Synthesis-related Genes in Indica Rice Cultivars
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作者 赵春芳 胡庆峰 +7 位作者 强新涛 赵凌 赵庆勇 陈涛 周丽慧 姚姝 梁文化 王才林 《Agricultural Science & Technology》 CAS 2016年第9期1993-1999,共7页
In this study, 34 molecular markers of starch synthesis-related genes were used to evaluate the genetic variation and population structure of 87 indica rice cultivars from different countries and regions. The results ... In this study, 34 molecular markers of starch synthesis-related genes were used to evaluate the genetic variation and population structure of 87 indica rice cultivars from different countries and regions. The results showed that a total of 80 alleles were amplified using 34 primer pairs, with an average of 2.5 alleles per locus. The allele number varied from 2 to 6 among various cultivars. Shannon's diversity index of molecular markers varied from 0.303 to 0.796, with an average of 0.539. Polymorphism information content (PIC) varied from 0.084 to 0.658, with an average of 0.295. The genetic similarity coefficients of 87 indica rice cultivars ranged from 0.265 to 0.990, indicating significant genetic differences of starch synthesis-related genes among different cultivars, but the variation frequency of alleles varied among different cultivars. Population structure analysis showed that these 87 indica rice cultivars were divided into three categories. Genetic differences were small within the same category but great among different categories. Moreover, indica rice cultivars with simple genetic components accounted for 39.1% and those with complex genetic background accounted for 60.9%. This study may not only provide theoretical basis for genetic improvement of rice starch quality, but also lay a solid foundation for subsequent association analysis of rice quality-related traits. 展开更多
关键词 Indica rice Starch synthesis-related gene Genetic variation Population structure
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Study on Chloroplast psbA-trnH Nucleotide Variation and Genetic Differentiation in Cultivated Plants of Gentiana officinalis from Qinghai
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作者 张得钧 高庆波 +1 位作者 李福安 李永平 《Agricultural Science & Technology》 CAS 2011年第10期1417-1419,1423,共4页
[Objective] The aim was to investigate the genetic diversity and analyze the genetic differentiation of germplasm resources of Gentiana officinalis H.Smith from Qinghai.[Method] The cpDNA of chloroplast psbA-trnH gene... [Objective] The aim was to investigate the genetic diversity and analyze the genetic differentiation of germplasm resources of Gentiana officinalis H.Smith from Qinghai.[Method] The cpDNA of chloroplast psbA-trnH gene was sequenced to analyze the genetic diversity of six populations of G.officinalis.[Result] A total of 10 distinct haplotypes were detected in the studied populations,and seven variable sites were found by comparing their sequences.G.officinalis with high-level genetic diversity(h=0.771).Genetic diversity was largely varied within populations,ranging from 0.563 to 0.857 for haplotype diversity,and from 0.002 43 to 0.005 83 for nucleotide diversity,respectively.Genetic differentiation among populations(Gst) of G.officinalis was 0.196 0;gene flow(Nm) was 2.05;80.40% of the genetic variability occurred within population.[Conclusion] The cultivated G.officinalis in Qinghai showed rich genetic diversity,which is beneficial for the production of high-quality herb medicine. 展开更多
关键词 Gentiana officinalis H.Smith cpDNA psbA-trnH Genetic diversity
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白化茶新品种“贵门白茶”的品种调查初报
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作者 付杰 夏小欢 +1 位作者 陈旭东 过红卫 《茶叶通讯》 2012年第1期27-28,共2页
白茶是一种低温情况下产生叶绿素缺失的遗传变异体,是茶树中的特异性品种。中国各地均有发现,如浙江安吉白茶。由于这种茶树代谢机能的特异性,早春低温时抑制了叶绿素的合成,但显著提高了游离氨基酸的生成量,因此,早春白茶的游离... 白茶是一种低温情况下产生叶绿素缺失的遗传变异体,是茶树中的特异性品种。中国各地均有发现,如浙江安吉白茶。由于这种茶树代谢机能的特异性,早春低温时抑制了叶绿素的合成,但显著提高了游离氨基酸的生成量,因此,早春白茶的游离氨基酸含量一般均在6%以上,更高者甚至达到9%以上,相比之下,同时期的其他绿茶品种的游离氨基酸含量只有2%~4%。 展开更多
关键词 安吉白茶 品种 调查初报 游离氨基酸含量 白化 遗传变异体 代谢机能 叶绿素
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Assessing the Germplasm of Laminaria (Phaeophyceae) with Random Amplified PoLymorphic DNA (RAPD) Method 被引量:9
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作者 赫英俊 邹俞萍 +3 位作者 王晓东 郑治国 张大明 段德麟 《Chinese Journal of Oceanology and Limnology》 SCIE CAS CSCD 2003年第2期141-148,共8页
Eighteen gametophytes includingL. japonica, L. ochotensisandL. longissima, were verified with random amplified polymorphic DNA (RAPD) technique. Eighteen ten-base primers were chosen from 100 primers selected for fina... Eighteen gametophytes includingL. japonica, L. ochotensisandL. longissima, were verified with random amplified polymorphic DNA (RAPD) technique. Eighteen ten-base primers were chosen from 100 primers selected for final amplification test. Among the total of 205 bands amplified, 181 (88.3%) were polymorphic. The genetic distance among different strains ranged from 0.072 to 0.391. The dendrogram constructed by unweighted pair-group method with arithmetic (UPGMA) method showed that the female and male gametophytes of the same cell lines could be grouped in pairs respectively. It indicated that RAPD analysis could be used not only to distinguish different strains ofLaminaria, but also to distinguish male and female gametophyte within the same cell lines. There is ambiguous systematic relationship if judged merely by the present data. It seems that the use of RAPD marker is limited to elucidation of the phylogenetic relationship among the species ofLaminaria. 展开更多
关键词 LAMINARIA GAMETOPHYTE RAPD germplasm identification.
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Improvement of Wild Rice Oryza Longistaminata through Mutation Induction 被引量:1
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作者 Fousseyni Cisse Medoune Papa Khouma 《Journal of Food Science and Engineering》 2016年第2期82-89,共8页
Influence of a mutation to improve the undesirable traits (shattering, red caryopsis etc.) of wild rice O. longistaminata while preserving its useful genes by radiation 20 Kr gamma rays from 60Co was studied. The mu... Influence of a mutation to improve the undesirable traits (shattering, red caryopsis etc.) of wild rice O. longistaminata while preserving its useful genes by radiation 20 Kr gamma rays from 60Co was studied. The mutants issued this irradiation were crossed with the interspecific variety SIK385-b-42-28-28 (O. glaberrima x O. sativa). Irradiation followed by crossing with interspecific variety generated a large genetic variability, in the subsequent generations, in plant height, maturity, non-shattering grain, kernel colour, spikelets fertility, panicle length, and grain size. This has resulted in identification of promising mutants which possess all the traits of cultivated rice O. sativa (white kernel, non-shattering grain, secondary branchies etc.). During 2012 rainy season, nineteen selected mutants from M5 and M7 generations were evaluated for yield potential in replicated trials at Longorola station. 展开更多
关键词 Wild rice Oryza longistaminata MUTAGENESIS mutants.
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Genetic variations of beta 2-adrenergic receptor gene are associated with essential hypertension in Xinjiang Kazakans
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作者 Zhi-Tao Yan Nan-Fang Li Jin Yang Ling Zhou Hui Liu Qin Luo 《Journal of Geriatric Cardiology》 SCIE CAS CSCD 2010年第1期52-57,共6页
Objective The aims of the present study were to investigate the associations of 46 A〉G, 79 C〉G, 491 C〉T and 659 C〉G genetic variants of the human beta 2-adrenergic receptor (β2-AR), ADRB2, gene with essential h... Objective The aims of the present study were to investigate the associations of 46 A〉G, 79 C〉G, 491 C〉T and 659 C〉G genetic variants of the human beta 2-adrenergic receptor (β2-AR), ADRB2, gene with essential hypertension (EH) in Xinjiang Kazakans population.Methods A gender-matched case-control (271 hypertensive cases and 267 normotensive controls) study was used to investigate the associations of the four variations in the coding region of ADRB2 with EH. The genotypes of the variants were identified by the polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP) methods. Results 46 A〉G, 79 C〉G and 659 C〉G polymorphisms were common in the Kazakan population, but 491 C〉T was a mutation (frequency ofT allele was only 0.003) and only found in EH group. The fxequency distributions of genotypes and alleles for 659 C〉G between the EH and control groups was significantly different (P〈0.05), while those for 46 A〉G and 79 C〉G polymorphisms were not statistically different. Logistic regression analysis suggested that the G allele of 659 C〉G polymorphism was a risk factor for hypertension (minor allele vs common homo; odds ratio, 13.240, 95% CI, 4.052-43.274; P〈0.05). Covariance analysis showed that systolic and diastolic blood pressure levels in GG+CG group of 659 C〉G were significantly higher than those in the CC group, but no significant difference of blood pressure were found between common homo and minor allele for 46 A〉G and 79C〉G polymorphisms. Haplotype analysis showed that two hyplotypes, HI: 46A-79C-491C-523C(48%)and H5:46A-79C-491C-659G, were associated with EH.Conelusion ADRB2 genetic variants may play independent roles in the molecular genetic mechanism of EH in Xinjiang Kazakans population (d Geriatr Cardio12010; 7:52-57). 展开更多
关键词 β2-adrenergic receptor gene variant essential hypertension HAPLOTYPE Xinjiang Kazakan
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Genetic interactions and modifi er genes in Hirschsprung's disease 被引量:5
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作者 Adam S Wallace Richard B Anderson 《World Journal of Gastroenterology》 SCIE CAS CSCD 2011年第45期4937-4944,共8页
Hirschsprung's disease is a congenital disorder that occurs in 1:5000 live births. It is characterised by an absence of enteric neurons along a variable region of the gastrointestinal tract. Hirschsprung's dis... Hirschsprung's disease is a congenital disorder that occurs in 1:5000 live births. It is characterised by an absence of enteric neurons along a variable region of the gastrointestinal tract. Hirschsprung's disease is classified as a multigenic disorder, because the same phenotype is associated with mutations in multiple distinct genes. Furthermore, the genetics of Hirschsprung's disease are highly complex and not strictly Mendelian. The phenotypic variability and incomplete penetrance observed in Hirschsprung' s disease also suggests the involvement of modifier genes. Here, we summarise the current knowledge of the genetics underlying Hirschsprung's disease based on human and animal studies, focusing on the principal causative genes, their interactions, and the role of modif ier genes. 展开更多
关键词 Neural crest Enteric nervous system Hirschsprung’s disease AGANGLIONOSIS Modif ier genes
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牦牛乳酸脱氢酶B基因突变体的克隆鉴定研究 被引量:5
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作者 郑玉才 赵兴波 +6 位作者 周静 朴影 金素钰 贺庆华 洪键 李宁 吴常信 《中国科学(C辑)》 CSCD 北大核心 2008年第2期131-135,共5页
通过聚丙烯酰胺凝胶电泳分析证实牦牛(Bos grunniens)乳酸脱氢酶存在两种类型,根据LDH同工酶谱的特点推测牦牛LDH多态是由B基因变异所致,并由此将凝胶电泳中迁移率快的LDH同工酶谱带称为LDH-Bf类型,迁移率慢的称为LDH-Bs类型.为阐明牦牛... 通过聚丙烯酰胺凝胶电泳分析证实牦牛(Bos grunniens)乳酸脱氢酶存在两种类型,根据LDH同工酶谱的特点推测牦牛LDH多态是由B基因变异所致,并由此将凝胶电泳中迁移率快的LDH同工酶谱带称为LDH-Bf类型,迁移率慢的称为LDH-Bs类型.为阐明牦牛LDH变异体的分子机制,实验从牦牛心脏组织中提取总RNA,采用RT-PCR方法分别克隆了LDH-Bf和LDH-Bs两种类型的B基因cDNA全长序列;序列比对分析发现LDH-Bf和LDH-Bs基因存在4个碱基差异;依据cDNA序列推导的氨基酸序列的比对分析,发现两者之间存在两个氨基酸差异;利用Deepview分子建模软件进行的牦牛H亚基及LDH1突变体的高级结构预测,发现突变的两个氨基酸都能产生新的H键,影响整个蛋白分子的H键网络,并进一步导致蛋白分子空间结构的变化. 展开更多
关键词 牦牛(Bos grunniens) 乳酸脱氢酶 遗传变异体 基因克隆 分子建模
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