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1.
试验通过研究卵巢摘除对布尔山羊杂种母羊羔肝脏、背最长肌、股二头肌中肌细胞生长抑制素(MSTN)和肌细胞生成素(MYOG)基因表达量的影响,旨在探讨去卵巢是否可以促进羔羊生长发育。将体重相近、长势良好的5月龄布尔山羊杂种母羊羔,随机分为处理组(n=20)和对照组(n=20)。试验初期摘除处理组母羊羔卵巢,对照组不摘除。饲养60d后,利用实时定量PCR法检测肝脏、背最长肌、股二头肌中MSTN和MYOG基因mRNA相对表达量。结果表明,卵巢摘除后,母羊股二头肌中MSTN基因mRNA相对表达量是对照组的8.73倍,差异极显著(P0.01),但背最长肌和肝脏中MSTN基因mRNA水平低于对照组(P0.05);处理组背最长肌和股二头肌中MYOG基因表达量极显著高于对照组的5.12倍和6.51倍(P0.01),肝脏中MYOG基因表达量为对照组的2.23倍(0.01P0.05)。可见,卵巢摘除可以上调背最长肌、股二头肌和肝脏中MYOG基因的表达以及股二头肌中MSTN基因的表达。  相似文献   

2.
试验旨在克隆山羊CMKLR1基因序列并进行生物信息学分析,研究其表达与肌内脂肪(IMF)沉积的相关性。采集山羊皮下脂肪组织,应用RT-PCR克隆山羊CMKLR1基因序列;以GAPDH(GenBank登录号:AJ431207.1)为内参基因,实时荧光定量PCR检测其在山羊不同组织中的表达量及在肌肉组织中的时序表达谱(以肝脏表达量为基准);测定肌肉组织中的IMF含量,分析其与CMKLR1 mRNA表达量的相关性。结果显示,克隆获得了山羊CMKLR1基因,1 089 bp的CDS区,GenBank登录号:KT165374。实时荧光定量PCR分析显示,CMKLR1基因在24月龄山羊心脏、肝脏、脾脏、肺脏、肾脏、脂肪、背最长肌、股二头肌和臂三头肌中均存在不同程度的表达,其中在肺脏中表达量显著高于其他组织(P< 0.05);CMKLR1基因在1~3和24月龄的山羊背最长肌、臂三头肌和股二头肌中表达趋势相同,均是在股二头肌中表达量最高,而8~10月龄则是在臂三头肌中表达量最高。山羊IMF含量以24月龄背最长肌含量最高。山羊背最长肌、股二头肌和臂三头肌中CMKLR1 mRNA表达与IMF含量相关性不显著(P> 0.05)。CMKLR1基因不参与山羊IMF沉积作用,试验结果为进一步研究CMKLR1基因奠定理论基础。  相似文献   

3.
为了研究赖氨酸对绵羊组织生长的影响,试验选用15只年龄、体重相近的杂交母羊(陶塞特♂×蒙古羊♀)随机分为3组,于基础日粮中分别添加不同水平的赖氨酸(0,4,10 g),采用Real-time PCR方法检测日粮不同赖氨酸水平对绵羊肝脏和背最长肌中GHR和IGF-ⅠmRNA表达的影响。结果表明:日粮赖氨酸水平影响绵羊肝脏和背最长肌中GHR和IGF-Ⅰ基因的表达,随日粮赖氨酸水平的提高肝脏GHR和IGF-ⅠmRNA及背最长肌IGF-ⅠmRNA表达量相应增加;背最长肌中4 g和10 g赖氨酸组GHR基因相对表达量均极显著高于对照组(P<0.01),10 g赖氨酸组的GHR基因相对表达量与4 g赖氨酸组间差异不显著(P>0.05)。说明添加一定量的赖氨酸可以调节绵羊组织的生长发育。  相似文献   

4.
为了研究生长轴激素对猪繁殖性能发育的影响,随机选取0、3、20、30、90、120、180日龄纯种二花脸公猪和大白公猪各4头,屠宰并采取睾丸组织样,以18S rRNA为内标,用相对定量RT-PCR法研究睾丸IGF-Ⅰ和IGF-IR mRNA的表达及发育性变化。结果表明,二花脸猪与大白猪睾丸IGF-ⅠmRNA表达的发育模式在30日龄前完全相同,即随着日龄的增加而呈极显著增加(P〈0.01);二花脸猪睾丸IGF-Ⅰ mRNA相对表达量在30-180日龄无显著变化;大白猪睾丸IGF-Ⅰ mRNA相对表达量在90日龄有所下降,而在120和180日龄又恢复到30日龄水平。二花脸猪睾丸IGF-Ⅰ mRNA相对表达量显著高于大白猪(P〈0.05)。二花脸猪与大白猪睾丸IGF-IR mRNA表达的发育模式不同。二花脸猪睾丸IGF-IR mRNA相对表达量在90-120日龄呈显著下降趋势(P〈0.05);大白猪IGF-IR mRNA相对表达量在0日龄较高,随后显著下降(P〈0.05),并在观察期内持续保持较低水平。二花脸猪IGF-IR mRNA相对表达量显著高于大白猪(P〈0.05)。睾丸IGF-Ⅰ mRNA和IGF-IR mRNA相对表达丰度呈极显著正相关(r=0.575,P〈0.01)。结论:(1)不同品种猪睾丸IGF-Ⅰ和IGF-IR mRNA表达具有特定的发育模式;(2)猪睾丸中IGF-Ⅰ和IGF-IR mRNA的协同表达可能对猪繁殖性能的发育有重要调节作用。  相似文献   

5.
《中国兽医学报》2017,(11):2175-2180
本研究旨在克隆山羊趋化因子(C-C基序)受体2(chemokine(C C motif)receptor-like 2,CCRL2)基因序列,并研究其组织和时序表达谱。以简州大耳羊为试验材料,应用RT-PCR方法克隆CCRL2基因并进行生物信息学分析,qPCR方法构建该基因在山羊不同组织表达谱和不同月龄背最长肌、股二头肌和臂三头肌中的表达水平,并将基因表达与IMF含量进行相关分析。结果显示:克隆得到山羊CCRL2基因(GenBank登录号:KT165378)长度为1 143bp,编码区长度为1 047bp;qPCR分析表明,CCRL2mRNA在24月龄山羊心、肝、脾、肺、肾、脂肪、背最长肌、股二头肌和臂三头肌中均有不同程度的表达,其中脾表达量最高(P<0.01);时序表达中,CCRL2基因在股二头肌和臂三头肌中的表达量均在8~10月龄极显著高于1~3和24月龄(P<0.01),在背最长肌中则为24月龄极显著高于1~3和8~10月龄(P<0.01);相关分析显示,股二头肌中CCRL2基因mRNA表达量与IMF含量呈极显著负相关(P<0.01)。CCRL2基因可能参与山羊IMF沉积作用。  相似文献   

6.
为了研究类胰岛素生长因子1(IGF-1)和类胰岛素生长因子1受体(IGF-1R)基因在绒山羊绒毛生长不同阶段皮肤组织中的表达差异,试验采用实时荧光定量PCR技术对非产绒期和产绒期辽宁绒山羊皮肤中IGF-1和IGF-1R基因的表达进行了测定。结果表明:辽宁绒山羊皮肤中IGF-1和IGF-1R mRNA的表达量在产绒期均极显著高于非产绒期(P<0.01),产绒期IGF-1、IGF-1RmRNA的表达水平分别是非产绒期的8.30倍和7.49倍。说明IGF-1和IGF-1R基因可能与山羊绒周期性生长有关。  相似文献   

7.
实验旨在探究Myf5、Myf6基因在黔北麻羊和努黔F_1代各组织间的相对表达水平。应用实时荧光定量PCR法检测Myf5、Myf6基因在黔北麻羊(3只)和努黔F_1代(3只)的心脏、肝脏、脾脏、肺脏、肾脏、背最长肌、股二头肌和臂三头肌等组织间的相对表达量。结果表明:各组织Myf5、Myf6基因在黔北麻羊和努黔F_1代间表达差异不显著;2种基因在黔北麻羊臂三头肌、股二头肌和背最长肌相对表达量均极显著高于肾脏、肝脏、心脏、脾脏、肺脏(P<0.01),其中Myf5基因在肾脏相对表达量显著高于脾脏和肺脏(P<0.05),Myf6基因在心脏和肝脏相对表达量均显著高于脾脏(P<0.05);2种基因在努黔F_1代臂三头肌、股二头肌和背最长肌相对表达量均极显著高于肝脏、肾脏、心脏、脾脏、肺脏(P<0.01),心脏和肝脏相对表达量均显著高于肺脏(P<0.05)。综上,Myf5、Myf6基因在黔北麻羊和努黔F_1代8种组织中均有表达且表达量不等,在肌肉组织中的表达量最高。  相似文献   

8.
为了研究不同育肥方式对欧拉型藏羊羔羊肌内脂肪与解偶联蛋白(UCP3)基因表达的关系,试验选取欧拉型藏羊羔羊背最长肌和股二头肌,测定肌内脂肪和UCP3基因mRNA的表达量。结果表明:试验组欧拉型藏羊羔羊背最长肌和股二头肌肌肉中UCP3基因mRNA显著高于对照组(P0.05),而试验组欧拉型藏羊羔羊背最长肌与股二头肌肌肉中UCP3基因mRNA的表达差异不显著(P0.05),对照组欧拉型藏羊羔羊背最长肌与股二头肌肌肉中UCP3基因mRNA的表达差异也不显著P0.05)。欧拉型藏羊羔羊背最长肌中UCP3基因表达量与其肌肉中肌内脂肪(IMF)的含量呈负相关(r=-0.326,P=0.368),股二头肌肌肉中UCP3基因表达量与其肌肉中IMF的含量呈负相关(r=-0.312,P=0.269)。说明UCP3基因可作为与胴体性状相关的候选基因。  相似文献   

9.
为研究赖氨酸对绵羊生长的影响及其机理,选用1岁左右的绵羊15只,平均分为A、B和C组.3组分别在基础日粮中添加0、4和10g赖氨酸盐酸盐.饲喂28 d后全部屠宰,取肝脏和背最长肌样,提取组织总RNA,反转录后扩增胰岛索样生长因子-I(IGF-I)和GAPDH基因,用荧光定量PCR法分析不同处理肝脏和背最长肌IGF-I基因的表达量.结果表明:C组IGF-I基因的相对表达量极显著高于B组(P<0.01),B组IGF-I基因的相对表达量极显著高于A组(P<0.01),说明添加一定量的赖氨酸呵以调节绵羊组织的生长发育.  相似文献   

10.
为探究FASN基因在贵州黑山羊不同肌肉组织中调控脂肪沉积的作用,采集12月龄公、母贵州黑山羊胸肌、背最长肌、肱三头肌、臂股二头肌,运用实时荧光定量PCR法(qPCR)检测FASN基因表达量,酸水解法测定肌内脂肪(IMF)含量,并通过Pearson分析FASN基因表达量与IMF含量相关性。结果显示,FASN基因在公、母羊不同组织中表达量均为臂股二头肌>胸肌>肱三头肌>背最长肌,其中公羊臂股二头肌显著高于背最长肌,母羊臂股二头肌极显著高于背最长肌;相同组织比较,母羊胸肌、肱三头肌、臂股二头肌表达量均高于公羊,背最长肌表达量低于公羊,但均未达到差异显著水平。IMF含量测定发现,公、母羊4个组织中IMF含量均为臂股二头肌>胸肌>肱三头肌≥背最长肌,同性别各组织之间比较差异不显著;相同组织比较,母羊4个组织中IMF含量均高于公羊。FASN基因表达量与IMF含量相关性分析表明,公、母羊FASN基因表达量与胸肌IMF含量呈正相关,与背最长肌、肱三头肌、臂股二头肌IMF含量呈负相关。  相似文献   

11.
蓝塘仔猪IGF-1水平与组织IGF-1、GHR基因的表达   总被引:4,自引:5,他引:4  
32头不同日龄(出生、3、21、35d)蓝塘仔猪,由前腔静脉采血后剖杀,取肝脏、背最长肌样品。用RIA法测血液、组织中IGF 1浓度,用放射受体法(RBA)检测肝脏、肌肉组织中GHR结合活性,用实时荧光定量PCR法检测IGF 1、GHRmRNA的表达水平。结果表明:(1)血液中IGF 1在出生日显著高于其它时期(P<0 05)。肌肉组织中IGF 1含量高于肝脏组织,肌肉组织IGF 1含量在3、21、35日龄时都显著高于出生日(P<0 05)。(2)肝脏细胞膜GHR结合活性在出生日显著高于3、21日龄(P<0 05),肝脏细胞膜GHR结合活性高于肌肉组织。(3)肝脏组织IGF 1、GHRmRNA的表达量均显著高于肌肉组织(P<0 05)。肝脏IGF 1mRNA的表达在出生日、21日龄时显著高于3、35日龄(P<0 05),GHRmRNA的表达在出生日显著高于其它日龄(P<0 05)。肌肉IGF 1、GHRmRNA的表达在出生日均显著高于其它日龄(P<0 05)。  相似文献   

12.
探讨IGF-2及IGF-1R蛋白质在子宫蓄脓的表达及与子宫蓄脓发病的相关性。采用免疫组织化学PV法与Western blotting检测5例正常子宫内膜(对照组)、19例子宫蓄脓(试验组)子宫内膜组织中IGF-2及IGF-1R的表达情况。结果表明,免疫组化与Western blotting检测结果一致,IGF-2和IGF-1R在蓄脓子宫组中的表达量极显著高于正常子宫(P<0.01)。对子宫蓄脓组中IGF-1R与IGF-2进行相关性分析,免疫组化结果表明IGF-1R与IGF-2之间低度相关(=0.423),Western blotting结果显示IGF-1R与IGF-2之间高度相关(=0.927)。结果提示,IGF-2阳性表达上调及IGF-1R的异常高表达,在子宫蓄脓的发生和发展过程中可能具有重要作用。  相似文献   

13.
To investigate the expression of IGF-2 and IGF-1R protein in endometria of canine pyometra and analyze the possible correlation with the incidence of canine pyometra.Immunohistochemistry PV method and Western blotting were used to measure the IGF-2 and IGF-1R expression characteristic of 5 normal endometria and 19 endometria of canine pyometra.The results showed that the IGF-2 level of endometria from pyometra group was extremely significant higher than that of control group by immunohistochemistry and Western blotting (P<0.01).The positive expression rate of IGF-1R in endometria of canine pyometra compared with that in the normal endometria was extremely significant higher by immunohistochemistry and Western blotting (P<0.01).The correlation analysis of IGF-2 and IGF-1R in canine pyometra showed that the result of immunohistochemistry was low correlation (=0.423), the result of Western blotting was high correlation (=0.927).The data suggested that increased expression of IGF-2 and IGF-1R played an important role in occurrence of canine pyometra.  相似文献   

14.
IGF-1 plays a key role in the proliferation and differentiation of granulosa cells. However, the molecular mechanism of IGF-1 action in avian granulosa cells during follicle maturation is unclear. Here, we first studied IGF-1 receptor (IGF-1R) expression, IGF-1-induced progesterone production and some IGF-1R signaling pathways in granulosa cells from different follicles. IGF-1R (mRNA and protein) was higher in fresh or cultured granulosa cells from the largest follicles (F1 or F2) than in those from smaller follicles (F3 or F4). In vitro, IGF-1 treatment (10(-8)M, 36h) increased progesterone secretion by four-fold in mixed F3 and F4 (F3/4) granulosa cells and by 1.5-fold in F1 granulosa cells. IGF-1 (10(-8)M, 30min)-induced increases in tyrosine phosphorylation of IGF-1R beta subunit and phosphorylation of ERK were higher in F1 than in F3/4 granulosa cells. Interestingly, IGF-1 stimulation (10(-8)M, 10min) decreased the level of AMPK Thr172 phosphorylation in F1 and F3/4 granulosa cells. We have recently showed that AMPK (AMP-activated protein kinase) is a protein kinase involved in the steroidogenesis in chicken granulosa cells. We then studied the effects of AMPK activation by AICAR (5-aminoimidazole-4-carboxamide ribonucleoside), an activator of AMPK, on IGF-1-induced progesterone secretion by F3/4 and F1 granulosa cells. AICAR treatment (1mM, 36h) increased IGF-1-induced progesterone secretion, StAR protein levels and decreased ERK phosphorylation in F1 granulosa cells. Opposite data were observed in F3/4 granulosa cells. Adenovirus-mediated expression of dominant negative AMPK totally reversed the effects of AICAR on IGF-1-induced progesterone secretion, StAR protein production and ERK phosphorylation in both F3/4 and F1 granulosa cells. Thus, a variation of energy metabolism through AMPK activation could modulate differently IGF-1-induced progesterone production in F1 and F3/4 granulosa cells.  相似文献   

15.
This study verified the in vitro effects of IGF-1, FSH or both on caprine preantral follicle development and mRNA levels encoding IGF-1, IGFR-1 and FSHR. Secondary follicles were cultured for six days with FSH, IGF-1 or IGF-1+FSH. The results showed that IGF-1 and/or FSH addition did not influence follicular development for six days. The interaction between IGF-1 and FSH increased the mRNA levels of IGF-1 and FSHR, and FSH increased the expression of the IGFR-1 mRNA. Thus, IGF-1 and/or FSH increased IGF-1, IGFR-1 and FSHR mRNA levels in in vitro cultured caprine secondary follicles, but they did not influence their development after six days of in vitro culture.  相似文献   

16.
9日龄黄羽雌性肉鸡1 000只随机分为A、B、C、D 4个组,每组设5个重复,每个重复50只。在A、B、C、D组的日粮中分别添加剂量为0、80、120、160mg/kg的还原型谷胱甘肽(GSH),饲养期84 d。观察GSH对肉鸡生长性能、血清类胰岛素生长因子1(IGF-1)、T3、T4水平以及组织IGF-1 mRNA表达的影响。结果表明,(1)添加GSH的鸡只血中GSH水平显著高于对照组(A组);(2)添加GSH的鸡只平均体质量和平均日增重均高于A组,其中B组显著高于A组;(3)添加GSH的鸡只血中IGF-1水平显著高于A组,血中T3水平明显升高,T4水平有升高趋势;(4)各试验组肝脏IGF-1 mRNA的表达水平有所增高,但不明显。35d时,C组胸肌组织的IGF-1 mRNA表达水平显著性高于A组。结果提示,肉鸡饲粮中添加GSH可增强肝脏IGF-1的分泌和肌肉组织IGF-1 mRNA的表达,血中IGF-1水平升高,而促进鸡只生长。  相似文献   

17.
动物被毛生长是一个复杂的过程,受遗传、内分泌、营养及外界条件等各种因素的影响。而胰岛素样生长因子-1(insulin-like growth factor-1,IGF-1)是一种具有促进细胞增殖、分化,调节物质代谢等多种生物活性的多肽分子。研究结果发现,IGF-1对被毛/毛发生长的影响不仅局限于自身,同时介导一些细胞因子对被毛生长的调节作用。为阐明IGF-1在被毛/毛发生长方面的重要作用,文章就国内外IGF-1对动物被毛生长影响的研究进展进行综述。  相似文献   

18.
The present study evaluated somatotrophic gene expression in liver, muscle and adipose tissue 4 d after weaning, a time point corresponding to greatly reduced serum concentrations of insulin-like growth factor (IGF)-1 and IGF-2 in pigs. Two-week-old barrows were either cross-fostered to a sow (SOW, N = 8) or weaned and fed a phase 1 diet containing either 0 or 7% spray-dried plasma (NP, N = 8 and SDP, N = 8; respectively). Piglets were allocated such that two size groups were equivalently represented in each experimental group (small, 3.5–4.3 kg and large, 4.6–5.7 kg). Animals were weighed daily and sacrificed 4 d after weaning for blood and tissue collection. Daily gains of the SOW piglets were significantly greater than those of the weaned pigs for the first 3 d of the experiment (P < 0.0001). Weight gains in the SOW and SDP pigs between d 3 and 4 were equivalently elevated relative to the NP pigs (P < 0.0001). Serum IGF-1 and IGF-2 concentrations were decreased in both NP and SDP compared to SOW (P < 0.0001). Serum IGF-2 levels were significantly lower in small piglets (P = 0.006). A Weaning Group X Size interaction was noted for liver IGF-2 mRNA (P < 0.03), reflecting a higher level of expression in large SOW piglets relative to small SOW piglets. Weaning did not affect IGF-1, IGF-2, or growth hormone (GH) receptor mRNA levels in liver, muscle, or fat (P > 0.05). Liver IGF-binding protein (IGFBP)-3 and acid-labile subunit (ALS) mRNA levels also were unaffected by weaning. Small pigs had lower levels of liver ALS (P = 0.0003), muscle IGF-2 (P = 0.02), and muscle GH receptor (P = 0.006) mRNAs. In contrast, adipose tissue IGF-1 and IGF-2 mRNA levels were greatest in the small piglets (P = 0.001 and 0.029, respectively).  相似文献   

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