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1.
研究早胜牛类群A-FABP基因多态性及其与胴体品质和肉质性状的相关性。采用PCR-SSCP方法对5个早胜牛类群(庆阳类群、平凉类群、南德温与庆阳类群杂种、西门塔尔与平凉类群杂种、秦川牛与平凉类群杂种)的A-FABP基因进行多态性分析,分析基因型与胴体品质和肉质性状的相关性。结果显示,A-FABP基因第三外显子区存在c.408GC的突变,并检测到3种基因型GG、GC和CC。胴体性状相关分析表明,GG基因型的胴体重显著低于CC基因型(P0.05);GG基因型屠宰率极显著低于GC基因型(P0.01),显著低于CC基因型(P0.05);GG基因型净肉率显著低于GC基因型(P0.05);GG基因型的眼肌面积显著低于GC和CC基因型(P0.05)。肉质性状相关分析表明,GG基因型失水率显著高于CC基因型个体(P0.05);GG基因型剪切力极显著高于GC和CC基因型(P0.01);GG基因型蒸煮损失和pH均显著高于GC基因型(P0.05),极显著高于CC基因型(P0.01)。A-FABP基因突变位点可作为胴体性状和肉质性状遗传标记。  相似文献   

2.
Guo LY  Fu JL  Wang AG 《遗传》2012,34(7):879-886
文章采用CRS-RFLP技术对长白猪、大白猪和杜洛克猪3个品种的整合素β1基因第5外显子T32207C位点及第7外显子A35230G位点进行单核苷酸多态性分析,并将基因多态性与猪的产仔数进行关联分析。结果表明:32207多态位点的基因型效应对3个品种的总产仔数(TNB)和产活仔数(NBA)影响均不显著;35230多态位点的基因型效应对大白猪和长白猪头胎、二胎及所有胎次的TNB和NBA的影响达到显著(P<0.05)或者极显著水平(P<0.01),基因型GG、AG与AA对产仔数的影响存在差异,其效应为GG,AG>AA。可见整合素β1基因35230位点的G等位基因对大白猪和长白猪的产仔数性状有显著影响。  相似文献   

3.
目的:通过筛选3个贵州地方山羊种DQA1基因Exon3的SNPs位点并做相应的遗传变异分析,为今后山羊抗病育种及地方山羊品种的选育提供理论依据。方法:采用构建品种DNA池与直接测序的方法,对三个贵州地方山羊种群共514只个体的DQA1基因外显子3进行遗传变异分析。结果:在3个山羊品种中共筛选得到4个SNPs,G71A(同义突变)、T100C(Asn→Ser)、G202A(Pro→Leu)、A223G(Met→Thr)。生物信息学分析发现,G202A位点变异虽未引起mRNA二级结构的变化,但最小自由能降低,结构稳定性增强;DQA1基因Exon3的不同基因型的蛋白质二级结构中均不含有α螺旋。结论:三个贵州地方山羊种DQA1基因外显子3中含有较丰富的多态性,G202A位点变异在mRNA二级结构及蛋白质二级结构中与其他基因型具有较明显的差异。  相似文献   

4.
利用聚合酶链式反应-单链构象多态(PCR-SSCP)技术检测中国美利奴羊(Chinese Merino)心脏型脂肪酸结合蛋白基因(H-FABP)外显子2的单核苷酸多态性(SNPs)和遗传多态性,分析其与肌内脂肪(IMF)含量、肌纤维直径和肌纤维密度的相互关系,为该品种绵羊的分子标记辅助选择提供理论依据。结果显示,H-FABP基因外显子2有AA、AB和BB 3种基因型,AA型和BB型在778位均发生了C缺失,939位均发生了A→G转换,BB型还在789位发生了T→C转换,该突变导致所编码氨基酸发生了缬氨酸→丙氨酸的替换;BB型为IMF的优势基因型,与AB型相比差异显著(P<0.05),与AA型相比差异极显著(P<0.01);BB型对肌纤维直径存在负相关。结果提示,中国美利奴羊H-FABP基因外显子2具有多态性,该基因可能是中国美利奴羊肉质性状的主效基因,或者与控制这些性状的主效基因相连锁。  相似文献   

5.
根据GenBank中报道的猪apoA5基因序列设计2对引物,应用PCR技术从可乐猪肌肉组织基因组中扩增出了apoA5基因第三外显子的特异片段,采用直接测序法对apoA5基因进行单核甘酸多态性检测,并分析该基因与可乐猪12项肉质性状的关联性,结果表明:在可乐猪apoA5基因第三外显子上共检测到3个SNPs-突变位点:A~(226)G、G~(535)C、和C~(1514)T,其中A~(226)G和G~(535)C突变发生在编码区内,没有引起氨基酸的改变,为沉默突变。C~(1514)T突变发生在3'-UTR,χ~2检验表明,发现的3个多态位点均处于Hardy-Weinberg平衡状态(p0.05)。A~(226)G位点为低度多态,其余两个突变位点均为中度多态。最小二乘分析显示,apoA5基因第三外显子226位点AA基因型个体的肌内脂肪显著高于AG基因型个体(p0.05),535位点GG基因型个体的肉色显著高于CC和GC型个体(p0.05),1514多态位点与可乐猪肉质性状没有显著关系(p0.05)。  相似文献   

6.
目的:探讨固醇调节元件结合蛋白-1c基因18号外显子54G/C基因多态性与新疆地区汉族人群心肌梗死的相关性.方法:采用聚合酶链反应-限制性片段长度多态性方法,对230例急性心肌梗死患者和212例健康受试者SREBP-1c基因18号外显子54G/C位点进行分析,同时进行血糖及血脂水平检测.数据处理利用PEMS for windows 3.1软件包完成,用Hardy-Weinberg平衡检验样本的群体代表性,各组基因型和等位基因频率差异比较用x2检验,连续变量的比较用t检验.结果:SREBP-le基因18号外显子54G/C在病例组和健康对照组中基因型频率分别为:CC型13.04%和4.25%,CG型34.78%和36.32%,GG52.17%和59.43%.两组CC基因型差异具有统计学意义(P<0.05),且病例组C等位基因频率高于对照组(P<0.05),而GC和GG基因型差异羌统计学意义(P<0.05).不同基因型问血糖、血脂水平差异具有统计学意义(P<0.05).结论:CC基因型和等位基因C可能增加急性心肌梗死发生的风险,并可影响病人的血糖、甘油三酯代谢.  相似文献   

7.
目的:对新疆4个绵羊品种内皮型一氧化氮合酶(eNOS)基因第8外显子的多态性进行鉴定。方法:利用PCR-SSCP和测序的方法对76只中国美利奴羊、51只无角陶赛特羊、57只萨福克羊、37只哈萨克羊共4个绵羊品种进行单核苷酸多态性(SNP)检测,并用生物信息学方法对检测出的SNP进行统计分析。结果:在中国美利奴羊、无角陶赛特羊、萨福克羊、哈萨克羊中共检测到AA、AB、BB等3种基因型,AA基因型的频率分别为0.0526、0.0980、0.1754和0.2973,BB基因型的频率分别为0.6316、0.1961、0.5614和0.1892,AB基因型的频率分别为0.3158、0.7059、0.2632和0.5135。通过测序,在eNOS基因第8外显子上发现了一个新的SNP位点(ss974768653),位于绵羊eNOS基因第8外显子142 bp处(A142G)。结论:中国美利奴羊和哈萨克羊的多态性位点(P0.05)处于Hardy-Weinberg平衡状态,萨福克和无角陶赛特羊的多态性位点(P0.05)不处于Hardy-Weinberg平衡状态。  相似文献   

8.
目的:探讨细胞毒性T淋巴细胞相关抗原-4(CTLA-4)+49 AG位点多态性与结直肠癌发生的相关性,为早期预测结直肠癌的发生提供临床参考依据。方法:选取结直肠癌病例231例未实验组和正常健康体检者325例为对照组,取其空腹外周静脉血提取DNA后,采用聚合酶链式反应(PCR)技术对CTLA-4基因第1外显子区+49位点DNA进行扩增,产物用限制性片段长度多态性(RFLP)方法检测CTLA-4第1外显子区+49AG位点的多态性,比较两组杂合子AG和纯合子AA、GG基因型发生的频率、A等位基因与G等位基因的分布,分析CTLA-4+49 AG位点多态性与结直肠癌发生的相关性。结果:两组间CTLA-4基因外显子1区+49AG位点杂合子AG和纯合子AA、GG基因型发生的频率以及A等位基因与G等位基因的分布比较差异均无统计学意义(P0.05)。结论:CTLA-4基因外显子1区+49 AG基因多态性与我省汉族人群结直肠癌的发病无显著相关性。  相似文献   

9.
粘蛋白MUC1 568A/G SNP与辽宁地区人群胃癌遗传易感性的关系   总被引:2,自引:1,他引:1  
徐倩  孙丽萍  宫月华  徐莹  董楠楠  袁媛 《遗传》2008,30(9):1163-1168
为了探讨粘蛋白(MUC1)基因568位点A/G单核苷酸多态性与胃癌遗传易感性的关系, 采用序列特异性引物-聚合酶链反应(Sequence specific primers PCR, PCR-SSPs)检测来自辽宁地区人群138例胃癌患者及与其配比的131例对照个体MUC1 568 位点A/G多态性, 以ELISA法检测血清H. pylori IgG抗体。结果显示:(1)对照人群MUC1基因568位点AA、AG、GG 3种基因型分布频率分别为73.3%、22.1%、4.6%; (2)胃癌组MUC1 AA基因型携带频率显著高于正常对照组(P=0.03), 携带MUC1 AA基因型个体胃癌的发病风险增高到1.92倍; (3)以MUC1 AG+GG基因型并血清幽门螺杆菌(H. pylori)IgG抗体阴性的个体为对照, AG+GG基因型并H. pylori IgG抗体阳性个体、AA基因型并H. pylori IgG抗体阴性个体、AA基因型并H. pylori IgG抗体阳性个体胃癌患病风险增高, 但3组各组间差异均无统计学意义(P>0.05)。说明MUC1基因568位点A/G多态与胃癌的遗传易感性相关; MUC1 A/G基因多态性和H. pylori感染在胃癌发生发展过程未见交互作用。  相似文献   

10.
激素敏感脂肪酶(Hormone-sensitive lipase,HSL)是负责分解脂肪组织中甘油三酯释放游离脂肪酸的关键和限速酶,也是影响动物脂肪沉积的关键酶.将HSL基因作为影响猪脂肪代谢和沉积相关性状的候选基因,对不同品种猪HSL基因5’-UTR和外显子Ⅰ片段进行了克隆测序并开展多态性与性状间的关系研究.序列比较发现,在测定的HSL基因靠近起始密码子(ATG)的419 bp中,杜洛克、梅山猪、大白猪和平序列完全一致,与长白猪序列比较,在-13~-12 bp位置存在GC→CG的碱基变异;梅山猪(3个体)、通城猪(3个体)、长白猪(3个体)、大白猪(3个体)HSL基因外显子Ⅰ的442 bp位置有G→A碱基间的变异,G→A的转换改变了限制性内切酶BsaHⅠ酶识别位点,且导致了编码氨基酸Val→Ile的替换.经PCR-RFLP分析,HSL基因外显子Ⅰ BsaHⅠ位点多态性有AA、AG和GG 3种基因型.”大白×梅山”F2代资源家系BsaHⅠ点不同基因型个体背膘厚、肌内脂肪等性状协方差统计分析发现,AG基因型和GG基因型在眼肌面积上存在显著差异.  相似文献   

11.
The adipocyte-type fatty acid-binding protein (A-FABP) is considered a candidate gene for fat metabolism; thus, it affects fat deposition in chickens. The present study was designed to examine the polymorphism and mRNA abundance of the A-FABP gene with intramuscular fat (IMF) in the pectoralis muscles (PM) and leg muscles (LM) of Three-yellow Chicken (TYC) and Hetian-black Chicken (HTBC). In total, 60 TYCs and 60 HTBCs were sacrificed using exsanguination at market age. The IMF contents of the PM and LM in the HTBC were significantly higher than those in the TYC. Three genotypes of the A-FABP gene first exon, AA, AB, and BB, were examined by polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP), and a C51 T mutational site, which is a silent substitution mutation, was revealed. The IMF contents of the AA genotype in the PM of the HTBC were significantly higher than those in the AB genotype; thus, the C51 T mutable site is a gene marker for selecting a higher IMF content in the PM of the HTBC. The relative expression of the A-FABP mRNA in the LM of the HTBC, which was measured by quantitative real-time PCR, was significantly higher than in the TYC. A significantly positive association was detected between A-FABP expression with the IMF contents of the PM and LM of both the TYC and the HTBC. These results provide basic data that might be helpful to further research the role of the A-FABP gene in fat deposition and fatty acid metabolism in chickens.  相似文献   

12.
西部地区主要猪种和野猪H-FABP基因分子标记   总被引:12,自引:0,他引:12  
庞卫军  孙世铎  李影  陈国柱  杨公社 《遗传》2005,27(3):351-356
利用PCR-RFLP(Hinf I、Hae Ⅲ和Msp I 3种限制性内切酶)分子标记技术,检测了杜洛克猪、长白猪、大白猪、内江猪、荣昌猪、汉江黑猪、汉中白猪、八眉猪和野猪共计265头猪H-FABP基因5′-上游区和第二内含子区的遗传变异,并利用最小二乘模型分析了H-FABP基因对猪肌内脂肪含量的遗传效应。结果表明:(1)在Hinf I-RFLP位点上,上述品种和野猪均存在多态性,其中大白猪、八眉猪、汉江黑猪、汉中白猪和野猪表现为低度多态,杜洛克、长白猪、内江猪和荣昌猪为中度多态;除汉江黑猪(P<0.05)和野猪(P<0.01)外,其他猪种基因频率和基因型频率都处于Hardy-Weinderg平衡状态(P>0.05);而在Hae Ⅲ-RFLP和Msp I-RFLP位点上,仅内江猪、荣昌猪、汉江黑猪和八眉猪为单态;(2)9种基因型对肌内脂肪(IMF)含量的影响,HH>Hh>hh,DD相似文献   

13.
猪H-FABP基因多态性与肌内脂肪含量的关联分析   总被引:2,自引:0,他引:2  
以山西白猪为实验材料,采用索氏脂肪抽提法对其背最长肌的肌内脂肪含量进行了测定。根据心脏脂肪酸结合蛋白(heart fatty acid-binding protein,H-FABP)基因的PCR-RFLP多态性,应用SPSS软件,用最小二乘法拟合一般线性模型(GLM)分析了H-FABP基因的不同位点的基因型对肌内脂肪含量的影响。结果表明,基因型hh、dd、BB对肌内脂肪含量影响的效应值最大。证明H-FABP基因可以作为肌内脂肪含量的侯选基因。  相似文献   

14.
He J  Chen J  Lu L  Tian Y  Tao Z  Wang D  Li J  Li G  Shen J  Fu Y  Niu D 《Molecular biology reports》2012,39(2):1073-1077
Liver-type fatty acid-binding protein (L-FABP) is a member of intracellular lipid-binding proteins involved in the transportation of fatty acids. We detected the polymorphisms of duck L-FABP gene and its association with the intramuscular fat (IMF) and other fat-related traits. The complete sequence of duck L-FABP gene (four exons and three introns, 2,542?bp) was obtained in this study. The polymorphism of L-FABP gene was examined with direct DNA sequencing method in 231 individuals from different breeds, and a novel single nucleotide polymorphism in the exon 3 was detected. The polymorphism was shown to be associated with the contents of C16:0, C18:3 and the total IMF in pectoral muscle. The content of C16:0 in genotype CC was significantly higher than CT (P?<?0.01) and TT (P?<?0.01), and the genotype CT was higher than TT (P?<?0.01). The content of C18:3 in genotype TT was significantly higher than CC and CT (P?<?0.01), whereas the genotype CC and CT had no significant difference (P?>?0.05). The content of IMF in genotype CC was significantly higher than CT (P?<?0.01). However, no significant difference was detected between genotype CC and TT or genotype CT and TT (P?>?0.05).  相似文献   

15.
H-FABP基因的多态性和营养因素对猪肉质的影响   总被引:4,自引:0,他引:4  
李长龙  萨晓婴  孟和  潘玉春 《遗传》2009,31(7):713-718
遗传和营养因素都能影响猪肉的品质。但是, 到目前为止同时研究遗传和营养因素对肉质影响的报道很少。在本研究中, 136头PIC5系杂交猪, 体重65 kg, 被随机分成4组, 各组分别给予不同日粮。在饲养35 d、体重大约90 kg时统一屠宰并且进行肉质测定、H-FABP基因分型及其与肉质性状的关联分析。结果表明: (1)所采用的3种日粮对肉色、屠宰后24 h的pH、肌内脂肪和肌肉蛋白含量有极显著的影响; (2)H-FABP基因型对肌内脂肪和肌肉蛋白含量存在极显著的影响; (3)H-FABP基因多态性和营养因素的交互作用对pH 和肌内脂肪含量均有显著的影响, 对照组的AA基因型具有最高pH值, 高维生素E组的AA基因型具有最高肌内脂肪值。实验结果提示在关于猪肉质的育种和生产过程中应该同时考虑营养因素和遗传因素。  相似文献   

16.
The examination of people belonging to the Russian ethnic group revealed that 20.3% of subjects had heterozygous genotype, containing the C-allele in single nucleotide polymorphism rs11562975, located in exon 7 of the gene encoding the temperature-sensitive ion channel TRPM8. Functional differences, associated with sensitivity to cold and menthol were identified between subjects with different genotypes of the polymorphism rs11562975 (GG and GC). Subjects with heterozygous genotype GC were characterized by increased sensitivity to cold and reduced sensitivity to menthol, agonist of the ion channel TRPM8, compared with subjects with homozygous genotype GG.  相似文献   

17.
庞卫军  白亮  杨公社 《遗传学报》2006,33(6):515-524
H-FABP是FABP家族成员之一,在长链脂肪酸的吸收和代谢平衡中发挥关键作用,但它对猪IMF含量的影响还知之甚少,对中国西部地区的猪种更是如此.文章利用PCR-RFLP(HinfⅠ、HaeⅢ和Msp Ⅰ 3种限制性内切酶)分子标记技术,检测了杜洛克猪、长白猪、大白猪、内江猪、荣昌猪、汉江黑猪、汉中白猪、八眉猪和野猪共计265头猪H-FABP基因5'-上游区和第二内含子区的遗传变异,利用最小二乘模型分析了H-FABP基因对猪肌内脂肪含量的遗传效应,并运用猪脂肪细胞培养,油红O染色和TG测定等技术检测了H-FABP基因不同基因型脂肪细胞内脂滴的形态和沉积的量.结果表明:(1)在HinfⅠ-RFLP位点上,上述品种和野猪均存在多态性,其中大白猪、八眉猪、汉江黑猪、汉中白猪和野猪表现为低度多态,杜洛克、长白猪、内江猪和荣昌猪为中度多态;除汉江黑猪(P<0.05)和野猪(P<0.01)外,其他猪种基因频率和基因型频率都处于Hardy-Weinderg平衡状态(P>0.05);而在HaeⅢ-RFLP和Msp Ⅰ-RFLP位点上,仅内江猪、荣昌猪、汉江黑猪和八眉猪为单态;(2)9种基因型对肌内脂肪(IMF)含量的影响,HH>Hh>hh,DD<Dd<dd,AA<Aa<aa,遗传效应值分别为:3.89,3.42,3.17,2.27,2.49,2.91,2.28,2.70,2.95,H-FABP基因可显著地提高IMF含量(P<0.05);(3)aaddHH型的脂肪细胞脂滴的形态,密度和含量与其他基因型细胞差异显著(P<0.05).结果提示:可通过提高"aaddHH"基因型的频率来增加IMF含量,达到改善猪肉质的目的.  相似文献   

18.
Osteoarthritis is a chronic progressive degenerative joint disease characterized by age-related regressive change in articular cartilage. A single nucleotide polymorphism has been described at position -174 of the interleukin-6 (IL-6) promoter region, leading to three possible genotypes, GG, GC, and CC. We investigated a possible association of the IL-6 -174G/C gene polymorphism with knee osteoarthritis in a Thai population. Genotype distributions and allelic frequencies of the IL-6 -174G/C polymorphism were investigated in 115 knee osteoarthritis patients and 100 healthy controls. Genotyping was performed using PCR-RFLP. The genotype distribution of IL-6 was 79 GG, 36 GC, 0 CC in knee osteoarthritis patients and 88 GG, 12 GC, 0 CC in controls. The frequency of the GC genotype in subjects with knee osteoarthritis was higher than in controls (P< 0.001). Logistic regression analysis showed that the GC genotype was independently associated with increased risk of knee osteoarthritis (odds ratio = 3.3, 95% confidence interval = 1.6-6.9, P = 0.001). These findings suggest that the -174G/C polymorphism of the IL-6 gene promoter plays a role in the pathogenesis of knee osteoarthritis.  相似文献   

19.
One QTL affecting backfat thickness (BF), intramuscular fat content (IMF) and eye muscle area (MA) was previously localized on porcine chromosome 6 in an F2 cross between Iberian and Landrace pigs. This work was done to study the effect of two positional candidate genes on these traits: H-FABP and LEPR genes. The QTL mapping analysis was repeated with a regression method using genotypes for seven microsatellites and two PCR-RFLPs in the H-FABP and LEPR genes. H-FABP and LEPR genes were located at 85.4 and 107 cM respectively, by linkage analysis. The effects of the candidate gene polymorphisms were analyzed in two ways. When an animal model was fitted, both genes showed significant effects on fatness traits, the H-FABP polymorphism showed significant effects on IMF and MA, and the LEPR polymorphism on BF and IMF. But when the candidate gene effect was included in a QTL regression analysis these associations were not observed, suggesting that they must not be the causal mutations responsible for the effects found. Differences in the results of both analyses showed the inadequacy of the animal model approach for the evaluation of positional candidate genes in populations with linkage disequilibrium, when the probabilities of the parental origin of the QTL alleles are not included in the model.  相似文献   

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