期刊文献+

肉鸡肠道PepT1 mRNA表达的肠段差异性与发育性变化 被引量:12

Regional and Ontogenetic Expression of PepT1 mRNA in Intestine of Broiler
下载PDF
导出
摘要 选用遗传背景相同的1日龄父母代雄性Arbor Acre(AA)鸡和父母代雄性岭南黄肉雏鸡各120羽,采用相对定量RT-PCR方法,以30 d时岭南黄鸡肠道样品为模板,研究肉鸡肠道寡肽转运载体1(Peptide transporter 1,PepT1)mRNA表达的肠段差异性;以AA肉鸡和岭南黄鸡十二指肠和空肠样品为模板,研究不同品种肉鸡肠道PepT1 mRNA表达的发育性变化.结果显示:(1)岭南黄肉鸡肠道PepT1 mRNA的表达丰度从十二指肠、空肠、回肠到结直肠依次降低,其中十二指肠显著高于结直肠(P<0.05);(2)AA鸡和岭南黄肉鸡PepT1 mRNA在十二指肠及空肠中的表达具有相同的发育模式,16 d表达丰度最高,16~44 d逐渐下降,58 d略微回升;不同基因型之间PepT1 mRNA丰度比较,AA鸡和岭南黄肉鸡两品种间PepT1 mRNA的表达没有显著差异(P>0.05).以上结果说明:(1)随着肠道空间位置的后移,岭南黄肉鸡肠道PepT1 mRNA的表达丰度逐渐降低,其中十二指肠的表达丰度显著高于结直肠(P<0.05);(2)不同品种肉鸡十二指肠及空肠PepT1 mRNA的表达具有相同的发育模式,且同日龄两品种间的表达丰度未见明显差异,表明PepT1 mRNA表达受到发育阶段的调控,但品种间具有稳定性. 120 1-day-old parental male Arbor Acre (AA) broiler and 120 1-day-old parental male Lingnan yellow broiler were randomly divided into 4 replicates, respectively. Regional expression of Peptide transporter 1 (PepT1) mRNA in different intestinal tract segments of Lingnan yellow broiler on 30 d and ontogeny of PepT1 mRNA in duodenum and jejunum of AA broiler and yellow broiler were determined by relative quantitative RT-PCR. The results showed that: (1) Regional expression of PepT1 mRNA in duodenum, jejunum, ileum and colorectum was declined gradually. The abundance of PepT1 mRNA in duodenum was higher than in colorectum (P〈 0.05); (2)Ontogeny patterns of PepT1 mRNA in duodenum and jejunum were consistent between AA broiler and Lingnan yellow broiler. The abundance of PepT1 mRNA in two strains was the highest on day 16, decreased from day 16 to day 44 and slightly increased again on day 58. While compared two breeds directly, the abundance of PepT1 mRNA in AA broiler was not significant difference than that in Lingnan yellow broiler from day 2 to day 58(P〉0.05). These results indicated that: (1) Regional expression of PepT1 mRNA in intestine of Lingnan yellow broiler was declined gradually along the downward intestine from duodenum, jejunum, and ileum to colorectum. The abundance of PepT1 mRNA in duodenum was higher than in colorectum (P 〈0.05) . (2) Ontogeny of PepT1 mRNA in two breeds had the same pattern in duodenum and jejunum, and there was no difference at same development stage between AA broiler and Lingnan yellow broiler, indicating that PeptT1 mRNA expression could be regulated by developmental stage but not breeds.
出处 《畜牧兽医学报》 CAS CSCD 北大核心 2007年第8期814-821,共8页 ACTA VETERINARIA ET ZOOTECHNICA SINICA
基金 "国家重点基础研究发展计划"(973)项目(2004CB117501) 国家自然科学基金(30671519)
关键词 肉鸡 肠道 PepT1 MRNA 肠道差异性表达 发育性表达 broiler intestine PepT1 mRNA intestinal regional expression ontogenetic expression
  • 相关文献

参考文献27

  • 1Barrett K E,Donowitz M.Gastrointestinal transport[M].New York:Academic Press,2001.379-402.
  • 2Daniel H.Molecular and integrative physiology of intestinal peptide transport[J].Annu Rev Physiol,2004,66:361-384.
  • 3Matthias B,Ilka K,Frederick H L.The intestinal H^+/peptide symporter PEPT1:structure-affinity relationships[J].European Journal of Pharmaceutical Sciences,2004,21:53-60.
  • 4Nicholas C Z,Ming T,Mark D.Molecular physiology of intestinal Na^+/H^+ exchange[J].Annu Rev Physiol,2005,67:411-443.
  • 5Fei Y J,Kanal Y,Nussberger S,et al.Expression cloning of a mammalian proton-coupled oligopeptide transporter[J].Nature,1994,368:563-566.
  • 6Liang R,Fei Y J,Prasad P D,et al.Human intestinal H^+/peptide cotransporter cloning,functional expression,and chromosomal localiztion[J].J Biol Chem,1995,270:6 456-6 463.
  • 7Satio H,Okudu M,Terada T,et al.Cloning and characterization of a rat H^+/peptide cotransporter mediating absorption of β-lactam antibiotics in the intestine and kidney[J].J Pharmacol Exp Ther,1995,275:1 631-1 637.
  • 8Fei Y J,Sugawara M,Liu J C,et al.cDNA structure,genomic organization,and promoter analysis of the mouse intestine peptide transporter PepT1[J].Biochim Biophys Acta,2000,1942:145-154.
  • 9Pan Y X,Wong E A,Bloomquist J R,et al.Expression of a cloned ovine gastro-intestinal peptide trans porter (oPepT1) in Xenopus oocytes induces uptake of oligo-peptides in vitro[J].J Nutr,2001,131:1 264-1 270.
  • 10Chen H,Pan Y X,Wong E A,et al.Molecular cloning and functional expression of a chicken intestinal peptide transporter (cPepT1) in Xenopus oocytes and Chinese hamster ovary cells[J].J Nutr,2002a,132:387-393.

二级参考文献15

  • 1王修启,张兆敏,张磊,陈杰,赵茹茜.日粮添加木聚糖酶对肉鸡小肠葡萄糖吸收及其转运载体基因表达影响[J].农业生物技术学报,2005,13(4):497-502. 被引量:16
  • 2Barfull A,Garriga C,Mitjans M and Planas J M.Ontogenetic expression and regulation of Na^+-D-glucose cotransporter in jejunum of domestic chicken (J).American Journal of Physiology,2002,282:G559~564
  • 3Cherbuy C,Darcy-Vrillon B,Posho L,Vaugelade P,Morel M T,Bernard F,Leturque A,Penicaud L and Duee P H.GLUT2and hexokinase control proximodistal gradient of intestinal glucose metabolism in the newborn pig (J).American Journal of Physiology,1997,272(6 Pt 1):G1530~539
  • 4Cui X L,Jiang L and Ferraris R P.Regulation of rat intestinal GLUT2 mRNA abundance by luminal and systemic factors (J).Biochemistry Biophysiology Acta,2003,1612(2):178~85
  • 5Dieffenbach C W (chief-editor).PCR Primer:A Laboratory Manual (2nd edition) (M).Cold Spring Harbor,New York:Cold Spring Harbor Laboratory Press,2003.
  • 6Ferraris R P.Dietary and developmental regulation of intestinal sugar transport (J).Biochemistry Journal,2001,360:265~276
  • 7Garriga C,Moreto M and Planas J M.Effects of resalination on intestinal glucose transport in chickens adapted to low Na+intakes (J).Experimental Physiology,2000,85(4):371~378
  • 8Kaput J and Rodriguez R L.Nutritional genomics:The next frontier in the postgenomic era (J).Physiological Genomics,2004,16:166~177
  • 9Kellett G L.The facilitated component of intestinal glucose absorption (J).Journal of Physiology,2001,531 (3):585~595
  • 10Khan J M,Wingertzahn M A,Teichberg S,Vancurova I,Harper R G and Wapnir R A.Development of the intestinal SGLT1transporter in rats (J).Molecular Genetics and Metabolism,2000,69:233~2399.O'Connor T P and Diamond J.Ontogeny of intestinal safety factors:Lactase capacities and lactose loads (J).American Journal Physiology Regulatory Integrative Compare Physiology,1999,276:753 ~ 765

共引文献8

同被引文献210

引证文献12

二级引证文献34

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部