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1.
POU1F1基因的遗传变异对南阳牛生长发育性状的影响   总被引:8,自引:0,他引:8  
利用PCR-RFLP技术首次研究了南阳牛群体100个个体POU1F1基因多态性及其与体重、体尺等生长性状指标之间的相关性。结果表明,南阳牛群体POU1F1基因座的451bp的PCR产物被限制性酶Hinf Ⅰ消化后表现多态性,它们的等位基因A/B频率为:0.465/0.535,且处于Hardy-Weinberg平衡状态。同时,南阳牛群体POU1F1-Hinf Ⅰ基因座不同基因型与体重、体尺等生长性状指标相关分析的结果表明:南阳牛群体内BB与AB基因型个体在初生重、断奶前平均日增重、六月龄体重、体斜长和胸围以及十二月龄的体重、体高、体斜长和胸围指标上有显著差异,且BB〉AB(P〈0.05);群体内BB型个体在十二月龄体重指标上显著高于群体的AA型个体,即BB〉AA(P〈0.05),在其他各年龄段的各项体重和体尺指标上同样呈现出B等位基因高于A等位基因的一种趋势。初步认为BB基因型为优势基因型,相应地B为优势等位基因,对选择有正向效应,提示POU1F1基因的占等位基因可能与高生长发育性状有关。  相似文献   

2.
Leptin基因的PCR-SSCP与牛体重、体尺指标的相关性   总被引:5,自引:0,他引:5  
利用PCR—SSCP技术研究了南阳牛、秦川牛、郏县红牛、西镇牛、鲁西牛和荷斯坦奶牛6个牛品种539个个体leptin基因的遗传多态性。结果表明,PCR扩增产物大小为330bp,PCR—SSCP分析表现出多态。南阳牛、秦川牛、郏县红牛、西镇牛、鲁西牛和荷斯坦奶牛的A等位基因频率分别为0.558,0.492,0.571,0.658,0.591,0.615;B等位基因频率分别为0.442,0.508,0.429,0.342,0.409,0.385。不同基因型与体重、体尺等生长性状指标相关性分析的结果表明:南阳牛群体内除12月龄的体高和日增重、18月龄的坐骨端宽和日增重外,BB型个体的六月龄、十二月龄、十八月龄、二十四月龄体斜长、胸围、体重、坐骨端宽、体高和日增重均显著的大于AB和AA型个体(P〈0.05);秦川牛群体内BB基因型个体十字部高上显著高于群体AA、AB型个体(P〈0.05),即BB〉AA、AB,可作为秦川牛体尺指标(十字部高)候选基因之一,但在体重、胸围、体长指标上均无显著差异(P〉0.05),所以不宜作为体重、胸围、体长指标候选基因;郏县红牛群体内AB与BB基因型个体在十字部高和坐骨端宽上显著高于群体AA型个体(P〈0.05),而群体内不同基因型在体重和体尺指标(体高、体斜长、胸围)上无显著差异(P〉0.05)。序列分析表明,leptin基因多态是第66位发生G→T、第67位发生A→C及299位发生新的单核苷酸突变C→T所造成。  相似文献   

3.
不同生长时期基因调控对南阳牛生长发育的影响   总被引:5,自引:0,他引:5  
高雪  徐秀容  任红艳  张英汉  许尚忠 《遗传》2006,28(8):927-932
以南阳牛为试验动物,利用PCR-SSCP和PCR-RFLP技术研究了南阳牛生长激素(GH)基因,IGF-I基因以及IGF-IBP3基因的遗传多态,并分析了遗传多态位点对南阳牛0月龄、6月龄、12月龄、18月龄、24月龄以及36月龄不同生长时期生长发育性状的影响。结果表明: 在6月龄~18月龄,GH基因的GH-P5位点的BB基因型对南阳牛的体长、体高显著的正效应;在生长的后期(24月龄~36月龄),IGF-IBP3-P5基因位点对南阳牛的后躯发育起主要调控作用,BB基因型个体的尻宽显著高于AA型。这表明基因的正效应不是在所有的生长周期表现,而是在特定的时期表现对南阳牛生长发育的显著影响。  相似文献   

4.
不同基因型对南阳牛生长发育性状的影响   总被引:2,自引:0,他引:2  
以南阳牛为实验动物,利用PCR-SSCP和PCR-RFLP技术研究了南阳牛生长激素(GH)基因,IGF-I基因以及IGF-IBP3基因的遗传多态,并分析了遗传多态位点对南阳牛0月龄、6月龄、12月龄、18月龄、24月龄以及36月龄不同生长时期生长发育性状的影响.结果表明: 在6月龄~18月龄,GH基因的GH-P5位点的BB基因型对南阳牛的体长、体高显著的正效应;在生长的后期(24月龄~36月龄),IGF-IBP3-P5基因位点对南阳牛的后躯发育起主要调控作用,BB基因型个体的尻宽显著高于AA型.这表明基因的正效应不是在所有的生长周期表现,而是在特定的时期内表现对南阳牛生长发育的显著影响.  相似文献   

5.
本研究以秦川牛及其与利木赞牛、德国黄牛以及红安格斯牛的杂交F_1代(4月龄)共4个牛群体总计164个个体为研究对象,以体尺性状作为衡量牛生长发育性状的指标,运用最小二乘线性模型,分析了10个SSR座位与生长发育性状的相关性.结果表明,10个多态SSR座位基因型对秦川牛及其杂交后代的生长发育性状效果不一:在ETH225座位,CH基因型(152/172)在4个群体内的体高、十字部高、尻长均显著低于其它基因型;BM1500座位,BC基因型(150/164)在十字部高、胸围、体重指标上高于BD型(150/170);HEL5座位,BD基因型(160/170)、EH基因型(172/180)在多项指标上大于其他基因型;BM2113座位,CG基因型(144/164)在体高、体长、腰角宽、胸围和体重指标上大于CF(144/160)、BF(142/160)基因型;CSSM66座位,BG基因型(183/211)在体高、十字部高、胸围指标高于AE基因型(181/207);HEL9座位BG基因型(158/178)在体高,十字部高、胸围、尻长和体重指标上大于EJ基因型(166/186).本研究的结果旨在为科学评价秦川牛的遗传资源价值和良种选育提供理论依据.  相似文献   

6.
牛POMC基因多态性及其与南阳牛生长性状的相关分析   总被引:3,自引:0,他引:3  
张春雷  王艳红  陈宏  雷初朝  房兴堂  王居强  马桂变  牛晖  肖杰 《遗传》2009,31(12):1221-1225
为研究阿片黑皮质素前体(POMC)在动物采食和能量平衡调控中发挥重要作用, 文章采用PCR-SSCP结合DNA测序方法, 对秦川牛、南阳牛、郏县红牛、晋南牛、鲁西牛、安格斯牛和荷斯坦奶牛共计480头个体POMC基因的多态性进行研究, 并分析了多态位点与南阳牛生长性状的相关性。结果表明, 牛POMC基因3个位点中, 在3′侧翼区P3位点新发现3个连锁存在的SNP(811845 C>T、811821 T>C和811797 A>G, 与NW_928357对照)。POMC基因3′侧翼区多态位点与南阳牛6月龄体重和0~6月龄平均日增重显著相关, BB型个体显著大于AA型(P<0.05)。  相似文献   

7.
阿黑皮素原(Pro-opiomelanocortin, POMC)在动物采食和能量平衡调控中发挥重要作用, 文章对绵羊POMC基因外显子3进行扩增和测序, 筛选多态性位点, 并分析多态位点与湖羊和东弗里生×湖羊杂种羊生长性状的相关性。测序后发现湖羊POMC基因外显子3有2个单碱基突变(g.273 T/C和g.456 G/A), 根据273位点处发生的T/C突变, 建立PCR-RFLP分析方法, 并对162只湖羊和130只东湖杂种羊进行检测分析。结果发现, 在湖羊群体中检测到TT(0.469)、TC(0.438)和CC(0.093)3种基因型, 而在东湖杂种羊群体中仅检测到TT(0.754)和TC(0.246)两种基因型。POMC基因外显子3的273位点多态性与生长性状的相关性研究结果显示:湖羊群体中CC基因型个体的2月龄断奶重、4月龄尻高及TC基因型个体4月龄体长和管围均显著高于TT型个体(P<0.05); CC基因型个体的4月龄重、6月龄重极显著高于TT和TC基因型个体(P<0.01); CC基因型个体的4月龄体高和体长极显著高于TT型个体(P<0.01), 且显著高于TC基因型个体(P<0.05)。此外, CC型个体的管围极显著高于TT基因型个体(P<0.01)。东湖杂种羊群体中TC基因型个体的2月龄断奶重、4月龄重及4月龄体高、体长、胸深和管围都显著高于TT型个体(P<0.05), TC型个体的6月龄重极显著高于TT型个体(P<0.01)。研究结果表明, POMC基因外显子3与绵羊生长性状相关, C等位基因对体重及体尺性状的增加更有利。该结果为进一步探讨POMC基因作为绵羊生长性状的辅助选育标记奠定了基础。  相似文献   

8.
秦巧梅  许尚忠  高雪 《遗传》2007,29(2):190-194
利用PCR-SSCP技术对南阳牛、利木赞、盖洛威共100头牛的生长激素受体基因的外显子10(GHR10)部分序列进行单核苷酸多态性研究, 并分析了该基因的不同基因型与3个品种牛生产性状的关系。结果表明: 南阳牛、利木赞、盖洛威3个品种中共存在6种基因型(AA、BB、CC、AB、AC、BC), c2检验表明该实验群体在这一位点上处于Hardy-Weinberg平衡状态(P > 0.05), 利木赞和盖洛威的PIC表现为中度多态,而南阳牛表现高度多态。测序结果显示: 所扩增GHR10部分片段共有5处碱基突变, 分别是495 bp (A/T), 622 bp(C/T), 650 bp(A/C), 702 bp(T/C), 730 bp(A/G); 并导致3处氨基酸替代: 其中622 bp Pro/Ser(脯氨酸/丝氨酸), 650 bp Asn/Thr(天冬酰胺/苏氨酸), 730 bp Ser/Gly(丝氨酸/甘氨酸)。最小二乘分析表明: 基因型AB、BC所对应的12月龄体重最小二乘均值显著高于基因型CC所对应的最小二乘均值(P < 0.05, P < 0.01); 18月龄体重BC基因型显著高于CC基因型(P < 0.01), 基因型AB所对应的18月龄胸围最小二乘均值显著高于基因型CC所对应的最小二乘均值(P < 0.05)。  相似文献   

9.
本研究采用PCR-SSCP技术和DNA测序法对大通牦牛、天祝白牦牛、甘南牦牛、普通牛4个群体CAPN4基因第6内含子的SNP多态性进行检测,并研究该基因在牦牛和普通牛群体中的遗传特征。试验所得表明:牦牛和普通牛CAPN4基因第6内含子表现出丰富的遗传多样性。CAPN4基因第6内含子检测到5种等位基因A-E,其中等位基因D和E仅存在于普通牛群体中。除天祝白牦牛外,等位基因B频率在其他3个牛群体中均在43%以上为优势等位基因。普通牛PIC0.25为低度多态外,3个牦牛群体PIC0.5为高度多态。  相似文献   

10.
跨膜蛋白18基因(TMEM-18)是一个末端为低聚嘧啶的基因,与动物生长发育密切相关。为了研究牦牛TMEM-18基因多态性与生产性能的关系。以192头天祝雌性牦牛血样NDA构建混合池,扩增TMEM-18基因内含子1和外显子5的序列。运用BLAST和Chromas软件分析突变位点,运用高分辨率熔解曲线分析技术(HRM)统计基因型分型,采用SHEsis软件进行基因型频率和等位基因频率计算,同时对多态位点进行配对连锁不平衡和单倍型分析,运用SPSS21.0分析基因多态位点与生产性能关联。结果表明,牦牛TMEM-18基因内含子1处存在2个多态位点,分别是861(A/G)和1267(C/T),外显子5处存在1个多态位点为4 447(C/T)。关联分析表明,牦牛TMEM-18基因861(A/G)位点的不同基因型与牦牛的体高、体重、胴体重和屠宰率差异性显著(P0.05);1267(C/T)位点的不同基因型与牦牛的体高、体重和屠宰率差异性显著(P0.05),而牦牛TMEM-18基因4447(C/T)位点的不同基因型与牦牛的体斜长、管围、胸围、体重、胴体重、净肉重、净肉率和屠宰率均存在显著性差异(P0.05)。通过单倍型分析发现群体中存在3种单倍型组合,即ACC单倍型、GTC单倍型和GTT单倍型,其中ACC单倍型组合个体数目明显多于其他单倍型组合,为优势单倍型。本实验揭示TMEM-18基因可作为牦牛生产性能开发的候选分子标记,为牦牛遗传资源的利用、开发与新品种的选育提供依据。  相似文献   

11.
Nine sheep breeds or strains, including 615 individuals were screened with forced PCR RFLP method for the FecB gene to study the polymorphism and its effects on litter sizes, body weights and body sizes. Results show that the polymorphism frequencies of FecB gene are significantly imbalanced in these breeds or strains. The Hu sheep were all homozygous carriers (BB). In the Chinese Merino prolific meat strain, the genotype frequencies of BB, B+ and ++ are 51%, 30% and 19%, respectively, whereas all the other flocks had only the wild-type (++) genotype. Results within Chinese Merino prolific meat strain showed that mean litter sizes of ewes with genotype BB and B+ are 2.8 (+/-0.74) and 2.3 (+/-0.63) (P > 0.05), whereas ++ ewes had a litter size of only 1.2 (+/-0.68) (P < 0.01). At 90 days after birth, the body weights of BB/B+ lambs were higher than that of ++ lambs (18.6 +/- 3.70 kg, 18.0 +/- 3.71 kg versus 15.6 +/- 2.22 kg, P < 0.05). In addition, the heart girth and chest width of BB/B+ lambs were significantly longer than ++ lambs (P < 0.05). No significant differences were observed in either body weight or body size at day 120. Litter size at first lambing from Hu at Natural Source Conservative Region was found to be significantly higher than that from the other two regions sampled (P < 0.05). In addition to the additive effect on litter size, these findings show for the first time that the FecB gene had a positive effect on early postnatal body growth.  相似文献   

12.
PCR–RFLP was applied to analyse polymorphisms within the MRF4 and heart fatty acid-binding protein (H-FABP) gene for correlation studies with growth traits in three-month-old Qinchuan (QQ), Qinchuan × Limousin (LQ) and Qinchuan × Red Angus (AQ) cattle. The results showed that 874 bp PCR products of MRF4 digested with XbaI and 2,075 bp PCR products of H-FABP digested with HaeIII were polymorphic in the three populations. Moreover, the frequencies of allele A at MRF4 locus and allele B at H-FABP locus in the QQ, AQ, and LQ populations were 0.8358/0.8888/0.8273 and 0.8358/0.7500/0.8195 respectively. Allele A at MRF4 locus and allele B at H-FABP locus were dominant in the three populations. No statistically significant differences in growth traits were observed among the genotypes of the all three populations at H-FABP locus. However, the association of MRF4 polymorphism with growth traits was then determined in all three populations. The body weight, withers height, heart girth and height at hip cross of individuals with genotype AA were higher than those with genotype AB or BB (P < 0.05). Therefore, we suggest that the MRF4 gene may function in the control or expression of growth traits, particularly body weight, withers height, heart girth and height at hip cross.  相似文献   

13.
Age at puberty and related phenomena were investigated in White Fulani (Bunaji - WF), Sokoto Gudali (SG) and Friesian X Bunaji (FRXWF) Zebu bulls from 28 weeks to 72 weeks of age. Pubertal traits studied included body weight, heart girth, scrotal circumference and sperm production. Puberty was defined as the age at which an ejaculated semen contained at least 50 x 10(6) spermatozoa with a minimum of 10% motility. Age at puberty was 66.89 +/- 1.0, 73.4 +/- 2.2 and 62.4 +/- 10.7 weeks for WF, SG and FRXWF bulls respectively. The Bunaji bulls were significantly younger than the Sokoto Gudali bulls at production of first motile sperm cell and also at puberty (P<0.01). The SG bulls were significantly heavier (P<0.01) and had larger heart girth (P<0.05) than the FRxWF at production of first motile sperm cells. Body weight and heart girth for all the breeds were not different at puberty (P>0.1). Scrotal circumference of the bulls between the breeds at production of first motile sperm cells and at puberty, did not differ (P 0.>1), despite the variations in age, weight and heart girth at production of first motile sperm cell and at puberty. It is concluded from the data obtained that the indigenous breeds of bulls (Bos indicus ) seem to attain puberty later than exotic breeds (Bos taurus ). The inter-play of genetic, nutritional and environmental factors as a contribution to this delay in attainment of puberty could not be ruled out.  相似文献   

14.
Animal and human data indicate a role for the peroxisome proliferator-activated receptor-gamma coactivator 1alpha (PPARGC1A) gene product in the development of maximal oxygen uptake (V(O2 max)), a determinant of endurance capacity, diabetes, and early death. We tested the hypothesis that the frequency of the minor Ser482 allele at the PPARGC1A locus is lower in World-class Spanish male endurance athletes (cases) [n = 104; mean (SD) age: 26.8 (3.8) yr] than in unfit United Kingdom (UK) Caucasian male controls [n = 100; mean (SD) age: 49.3 (8.1) yr]. In cases and controls, the Gly482Ser genotype met Hardy-Weinberg expectations (P > 0.05 in both groups tested separately). Cases had significantly higher V(O2 max) [73.4 (5.7) vs. 29.4 ml x kg(-1) x min(-1) (3.8); P < 0.0001] and were leaner [body mass index: 20.6 (1.5) vs. 27.6 kg/m2 (3.9); P < 0.0001] than controls. In unadjusted chi2 analyses, the frequency of the minor Ser482 allele was significantly lower in cases than in controls (29.1 vs. 40.0%; P = 0.01). To assess the possibility that genetic stratification could confound these observations, we also compared Gly482Ser genotype frequencies in Spanish (n = 164) and UK Caucasian men (n = 381) who were unselected for their level of fitness. In these analyses, Ser482 allele frequencies were very similar (36.9% in Spanish vs. 37.5% in UK Caucasians, P = 0.83), suggesting that confounding by genetic stratification is unlikely to explain the association between Gly482Ser genotype and endurance capacity. In summary, our data indicate a role for the Gly482Ser genotype in determining aerobic fitness. This finding has relevance from the perspective of physical performance, but it may also be informative for the targeted prevention of diseases associated with low fitness such as Type 2 diabetes.  相似文献   

15.
A total of 129 Limousin calves were used to investigate how leptin gene polymorphisms affect growth traits, such as body weight, average daily gain, wither height, sacrum height and chest girth in beef cattle. Two single nucleotide polymorphisms (SNPs) were genotyped, including the Sau3AI polymorphism in intron 2 and the A59V polymorphism in exon 3. The genotype and allele frequencies for each SNP and the haplotype frequencies for both SNPs were estimated in the studied herd. Statistical analysis revealed that the A59V polymorphism significantly affected the body weight at 210 days of age (P ≤ 0.01) and the average daily gain between 3 and 210 days of age (P ≤ 0.05) with T as a desirable allele. No associations were observed between the Sau3AI polymorphism and the growth traits mentioned above. However, the average daily gain between 3 and 210 days of age was significantly higher in the CT/CT haplotype animals compared with the CC/CC and CC/CT individuals. These results indicated that selection for the A59V TT animals might contribute to an improved body weight in Limousin cattle. The article is published in the original.  相似文献   

16.
Scrotal circumference as an index of testes size, along with body weight, wither height, heart girth and body condition score were measured fortnightly for 114 Menz ram lambs from weaning (91+/-7 SD days) until puberty, which was defined as age at first collection of an ejaculate with 50 x 10(6) spermatozoa and 10% motility. The animals were maintained on poor (n=28), low (n=29), medium (n=29) or high (n=28) levels of nutrition through grazing and supplementation. Further, half the lambs in each group were drenched for endoparasites. Daily gains in live weight, wither height, heart girth and scrotal circumference were 48.5+/-1.6 g, 0.05+/-0.01 cm, 0.07+/-0.01 cm and 0.07+/-0.03 cm, respectively for the period from weaning to puberty and varied with level of nutrition (P<0.05 to 0.001) but not with drenching or its interaction with nutrition level (P>0.10). Scrotal circumference increased linearly and was strongly correlated with age, body weight, wither height, and heart girth (r = 0.83 to 0.85, P<0.001), and lamb weight could be predicted by the equation: 6.35 + 0.53 scrotal circumference (R(2) = 0.73). Mean age, body weight and condition score at puberty were 288+/-6 days, 19.3+/-0.4 kg and 2.6+/-0.06, respectively, and varied due to season of birth, level of nutrition and weaning weight (P<0.01 to 0.001). The nutrition level also influenced (P<0.001) scrotal circumference at puberty, averaging 21.5+/-0.3 cm. It was concluded that postweaning nutrition management had a strong influence on lamb weight gain, which in turn was related to testicular growth and puberty onset in Menz ram lambs. The suitability of scrotal size measurement as a criterion for early selection of tropical ram lambs is emphasised.  相似文献   

17.
The allele and genotype distribution of two alcohol dehydrogenase genes ADH1B (exon 3 polymorphism A/G (47His)), ADH7 (intron 5 polymorphism G/C) and cytochrome P450 2E1 gene (CYP2E1; 5'-flanking region G/C and intron 6 T/A polymorphisms) were examined in Russian (Tomsk, n = 125) healthy population and in coronary atherosclerosis patients (CA, n = 92). The genotype frequencies followed the Hardy-Weinberg equilibrium and the alleles were in linkage equilibrium or gametic equilibrium in the control sample. Only two CYP2E1 gene polymorphisms were in linkage disequilibrium. The frequencies of the derived alleles at ADH1B (*G (+MslI) allele), CYP2E1 (**C2 (+PstI) allele) and CYP2E1 (*C (-Dra I)2 allele) were 8.48 +/- 1.86%; 1.20 +/- 0.69% and 10.00 +/- 1.90%, respectively. The 2ADH7 gene polymorphism showed a high level of heterozygosity; the frequency of the ADH7*C (-Sty I) allele was 44.58 +/- 3.21%. A significantly higher frequency of CYP2E1 (*C2 (+Pst I)) allele has been revealed in the CA group (P = 0.043; OR = 4.23; 95% CI 1.03-20.01). The tendency to significant effect of A1A2 genotype in ADH1B Msl 1 polymorphism was observed for systolic blood pressure in the control group (P = 0.068). The statistically significant two-way interaction effects of ADH7 StyI and CYP2E1 DraI on diastolic blood pressure (P = 0.029) and on the serum high density lipoprotein level (P = 0,042) were also revealed. Association of A1A2 genotype in ADHIB Msl I polymorphism with reduced amount in a serum of a very low density lipoprotein level (P = 0.045) have also been shown. This may result from multifunctional activity of alcohol metabolizing enzymes and their involvement in many metabolic and free radical reactions in the body.  相似文献   

18.
绝经后骨质疏松症(PMO)是一种多基因调控的遗传性疾病。雌激素受体β亚型基因是骨质疏松症的重要侯选基因。此文采用病例对照设计(78名股骨颈PMO病人和122名对照以及108名腰椎PMO病人和92名对照)研究中国人(汉族)雌激素受体β基因(ESR2)第5内含子CA重复序列多态性与PMO的相关性。以CA重复序列平均数22次为界将重复序列基因分为短基因(<22)和长基因(≥22),分别以S和L表示。股骨颈及腰椎(L2-4)部位,病例组中LL基因型和L等位基因者频率显著高于对照组(P<0.01),SL、LL及SL LL基因型者较SS基因型者患PMO风险显著增高(P<0.05);调整年龄、绝经时间、绝经年龄及体质指数后,Logistic回归分析显示ESR2(CA)n多态性仍然与股骨颈(OR4.923,95%CI1.986~12.203,P=0.001)及L2-4(OR2.267,95%CI1.121~4.598,P=0.023)PMO显著相关。结果显示:ESR2基因CA重复序列多态性与股骨颈和L2-4部位PMO独立关联,L等位基因显性影响PMO的发病风险。  相似文献   

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