摘要
应用RT-PCR及PCR分离到鲤鱼2个jlGHSR2s基因,jlGHSR2a和2b,分别编码366,367个氨基酸,相似性高达98%,和金鱼、斑马鱼GHSR2的相似性高达95%。jlGHSR2s基因的内含子位于起始密码子793 bp后,2a和2b内含子的长度和序列均存在明显差异。试验首次发现了jlGHSR2a的转录变体(Variant)jlGHSR2a',由选择性剪切靠近内含子的57 bp外显子1和保留靠近外显子2的28 bp内含子构成,编码350个氨基酸,缺失最后2个跨膜区,剪切序列两端碱基为CT-AC。荧光定量RT-PCR结果表明,jlGHSRs在脑和精巢表达量最高,1s在检测的组织均有表达,但2s在其他组织表达量很少。jlGHSRs的转录变体1s'和2a'的表达量与1s和2s有一定的正相关性,但1s/1s'在各组织不一致,比值最高出现在肝脏,其次是肌肉、肠和脑,精巢和卵巢最低。生长对脑中jlGHS-R1s的表达量没有显著影响,但生长慢的个体肝和肠中jlGHSR1s的表达量比生长快的高,1s/1s'也有明显升高;肌肉中则相反,1s/1s'在雄鱼肌肉中减小明显。饥饿使雌鱼脑、雌鱼前肠和雌雄鱼后肠jlGHSR1s的表达量显著降低,对其余组织中的表达则不显著。生长快慢或饥饿对脑中jlGHSR2s的表达量均没有显著影响。结果表明,jlGHSR1s的表达量与生长有明显的相关性。
Growth hormone secretagogue receptors ( GHSRs ) , the endogenous receptor of growth hormone se-cretion ( ghrelin) ,belong to G-protein-coupled receptors family ,and play a regulatory role on animal growth ,energy homeostasis etc.In this experiment,RT-PCR and PCR methods were applied to isolate two jlGHSR2s,jlGHSR2a and 2b,eccoding 366 and 367 amino acids sharing 98% identity with each other,and 95% identity with Danio rerio GHSR2.Intron of jlGHSR2s is located at 793 bp after start codon,there are obvious differences in length and se-quences between 2a and 2b introns.We first report jlGHSR2a′,the variant of jlGHSR2a,which is selectively spliced last 57 bp of exon 1 and reserved last 28 bp of intron near exon 2.jlGHSR2a′encodes 350 amnio acids,missing the last two transmembrane region ,and two ends of splicing sequence are CT-AC.Fluorescent quantitative RT-PCR re-sults showed that the highest expression level of jlGHSRs is in brain and testis ,1s is expressed in all the tissues ex-amined in this experiment ,but2 s is rarely expressed in other tissues .The expression of variants 1 s′and 2 a′has cer-tain degree of positive correlation with 1s and 2s,but 1s/1s′is inconsistent among these tissues ,the highest ratio is Growth hormone secretagogue receptors ( GHSRs ) , the endogenous receptor of growth hormone se-cretion ( ghrelin) ,belong to G-protein-coupled receptors family ,and play a regulatory role on animal growth ,energy homeostasis etc.In this experiment,RT-PCR and PCR methods were applied to isolate two jlGHSR2s,jlGHSR2a and 2b,eccoding 366 and 367 amino acids sharing 98% identity with each other,and 95% identity with Danio rerio GHSR2.Intron of jlGHSR2s is located at 793 bp after start codon,there are obvious differences in length and se-quences between 2a and 2b introns.We first report jlGHSR2a′,the variant of jlGHSR2a,which is selectively spliced last 57 bp of exon 1 and reserved last 28 bp of intron near exon 2.jlGHSR2a′encodes 350 amnio acids,missing the last two transmembrane region ,and two ends of splicing sequence are CT-AC.Fluorescent quantitative RT-PCR re-sults showed that the highest expression level of jlGHSRs is in brain and testis ,1s is expressed in all the tissues ex-amined in this experiment ,but2 s is rarely expressed in other tissues .The expression of variants 1 s′and 2 a′has cer-tain degree of positive correlation with 1s and 2s,but 1s/1s′is inconsistent among these tissues ,the highest ratio is
in the liver,followed by muscle,intestine and brain,testis and ovary are the minimum ones .Growth does no signifi-cant effect on the jlGHS R1s expression in brain,but jlGHSR1s expression in liver and intestine of slow growth is higher than fast growth ones, 1s/1s′is also increased obviously.It is opposite in muscle,1s/1s′in male muscle is obviously decreased.The growth speed or starvation could do no significantly effects on jlGHSR2 s expression in the brain.Our results show that the jlGHSR1s expression level is clearly correlated with growth .
出处
《华北农学报》
CSCD
北大核心
2013年第5期6-14,共9页
Acta Agriculturae Boreali-Sinica
基金
国家科技部"863"计划项目(2011AA100401)
公益性行业(农业)科研专项(200903045)
现代农业产业技术体系建设专项资金(CARS-46)
鲤肉质相关分子标记的挖掘项目(2013JBFM03)
关键词
建鲤
生长激素促泌素受体
转录变体
表达
Cyprinus carpio var. fian
Growth hormone secretagogue-receptor
Transcript variants
Expression