期刊文献+

仿刺参cytb和β-actin基因表达稳定性比较 被引量:29

Stability Comparison of cytb and β-actin Genes Expression in Sea Cucumber(Apostichopus japonicus)
下载PDF
导出
摘要 基因表达分析需要采用内参基因来校正目的基因的表达量。采用半定量RT-PCR的方法分析了cytb和β-actin基因在仿刺参(Apostichopus japonicus)未受精卵、受精卵、多细胞期、囊胚期、原肠期、小耳状幼体、中耳状幼体、大耳状幼体、樽型幼体、五触手幼体、稚参11个发育阶段和幼参的体壁、体腔细胞、肠道和呼吸树中的表达情况。结果表明:cytb在不同发育阶段和不同组织中稳定表达;β-actin基因在稚参之前不同发育阶段中表达水平有显著差异,在幼参的体壁、肠道和呼吸树中稳定表达。此外,cytb在lipopolysaccgarides(LPS)刺激前后的原肠胚、小耳状幼体、中耳状幼体、大耳状幼体、樽型幼体、稚参和幼参四种组织中表达量无显著差异;β-actin基因在LPS刺激前后的幼参体腔细胞、肠道和呼吸树中表达量无显著差异。本研究为仿刺参功能基因表达分析中,cytb与β-actin基因作为内参基因的可行性提供了依据。 Analysis of gene expression commonly uses internal control gene for normalization.The mRNA levels for cytb and β-actin genes were detected by using RT-PCR at 11 larval development stages of sea cucumber(Apostichopus japonicus)including unfertilized egg,fertilized egg,cellulous stages,blastula,gastrula,early auricularia,auricularia,late auricularia,doliolaria,pentactula,juvenile and in different tissues of young sea cucumbers including body walls,coelomocytes,intestines and respiratory trees.The results showed that cytb gene expression was stable at all development stages and in the four tissues.The mRNA levels for β-actin gene showed significant differences at different development stages,but were stable in the tissues of body walls,intestines and respiratory trees.Moreover,cytb mRNA showed no significant changes in expression after a LPS challenge at the stages of gastrula,early auricularia,auricularia,late auricularia,doliolaria and juvenile or in the four tissues of young sea cucumbers.The expression of β-actin gene was also stable in the tissues of coelomocytes,intestines and respiratory trees after a LPS challenge.This study provides information for the selection of cytb gene and β-actin gene as suitable internal control gene in target genes expressions research of sea cucumber.
出处 《中国农业科技导报》 CAS CSCD 2010年第1期79-84,共6页 Journal of Agricultural Science and Technology
基金 国家自然科学基金项目(30972272) 国家863计划项目(2006AA10A411) 国家海洋公益性行业科研专项(200705007) 辽宁省科技计划项目(2008203002)资助
关键词 仿刺参 CYTB基因 Β-ACTIN基因 LPS刺激 内参基因 sea cucumber(Apostichopus japonicus) cytb gene β-actin gene LPS challenge internal control gene
  • 相关文献

参考文献15

  • 1Ramirez-Gomez F, Ortiz-Pineda P A, Rojas-Cartagena C, et al.. Immune-related genes associated with intestinal tissue in the sea cucumber Holothuria glaberrima [ J ]. Immunogenetics, 2008,60( 1 ) :57 -71.
  • 2Rojas-Cartagena C, Distinct profiles of regeneration in the Physiol. Genomics Ortiz-Pineda P, Ramirez-Gomez F, et al.. expressed sequence tags during intestinal sea cucumber Holothuria glaberrima [ J ]. 2007, 31(2) :203 -215.
  • 3Lin S, Zhang H. Mitogen-activated protein kinase in Pfiesteria piscicida and its growth rate-related expression [ J ]. Appl. Environ. Microbiol. , 2003,69( 1 ) :343 -349.
  • 4赵丽媛,于志刚,甄毓,米铁柱.东海原甲藻线粒体细胞色素b(Cytb)基因的定量检测[J].中国海洋大学学报(自然科学版),2009,39(3):448-452. 被引量:8
  • 5何闪英,于志刚,米铁柱.增殖细胞核抗原基因表达量与中肋骨条藻生长的关系[J].水生生物学报,2009,33(1):103-112. 被引量:4
  • 6Schmittgen T D, Zakrajsek B A. Effect of experimental treatment on housekeeping gene expression:validation by real- time quantitative RT-PCR [ J ]. J. Bioehem. Biophys. Methods ,2000,46( 1 - 2 ) :69 - 81.
  • 7Yang A F, Zhou Z C, He C B, et al.. Analysis of expressed sequence tags from body wall, intestine and respiratory tree of sea cucumber ( Apostichopus japonicus ) [ J ]. Aquaculture, 2009,296 ( 3 - 4 ) : 193 - 199.
  • 8Halford W P. The essential prerequisites for quantitative RT- PCR[JI. Nat. Biotechnol. ,1999,17(9):835.
  • 9Thellin O, Zorzi W, Lakaye B, et al.. Housekeeping genes as internal standards : use and limits[J].J. Biotechnol. , 1999,75 (2 -3) :291 -295.
  • 10Goidin D, Mamessier A, Staquet M I, et al.. Ribosomal 18S RNA prevails over glyceraldehydes-3-phosphate dehydrogenase and beta-actin genes as internal standard for quantitative comparison of mRNA levels in invasive and noninvasive human melanoma cell subpopulations [ J]. Anal. Biochem. , 2001, 295(1) :17 -21.

二级参考文献60

  • 1王桂兰,黄秀清,蒋晓山,洪君超.长江口中肋骨条藻赤潮的分布与特点[J].海洋科学,1993,17(3):51-55. 被引量:20
  • 2陈凤花,王琳,胡丽华.实时荧光定量RT-PCR内参基因的选择[J].临床检验杂志,2005,23(5):393-395. 被引量:58
  • 3Furnas M J. In situ growth rates of marine phytoplankton: approaches to measurement, community and species of growth rates [J]. Journal of Plankton Research, 1990, 12:1117--1151
  • 4Matthews M B, Bernstein R N, Franza B R, et al. Identity of the proliferating cell nuclear antigen and cyclin [J]. Nature, 1984, 309 : 374--376
  • 5Bravo R, Frank R, Blundell P A, et al. Cyclin/PCNA is the auxiliary protein of DNA polymerase [ J]. Nature, 1987, 326: 515--517
  • 6Sasaki K, Kurose A, Ishika Y, et al. Estimation of S-phase fraction in tumor tissue sections by immunohistochemical staining of PCNA [ J]. Journal of Histochemlstry and Cytochemistry , 1994, 42 : 957--960
  • 7Lee C S, Redshaw A, and Boag G. Assessment of cell proliferation in human laryngeal cancers using proliferating cell nuclear antigen and Ki-67 antigen immunostaining [J]. Cell Vision, 1995, 2:296--300
  • 8Kodama H, Ito M, Ohinishi N, et al. Molecular cloning of the gene for plant proliferating cell nuclear antigen and expression of this gene during the cell cycle in synchronized culture of Catharanthus roseus cells [ J ]. European Journal of Biochemistry, 1991, 197:495--503
  • 9Lin S, Carpenter E J. Growth characteristics of phytoplankton determined by cell cycle proteins : The cell cycle of Ethmodiscus rex in the southwestern North Atlantic Ocean and Caribbean Sea [J]. The Journal of Physiology, 1995, 31:778--785
  • 10Lin S. Chang J, Carpenter E J. Detection of proliferating cell nuclear antigen analog in four species of marine phytoplankton [ J]. The Journal of Physiology, 1994, 30 : 449-- 456

共引文献24

同被引文献425

引证文献29

二级引证文献102

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