Quantitative reverse transcription and polymerase chain reaction analysis of oxytocin and vasopressin receptor mRNAs in the rat uterus near parturition

被引:11
|
作者
Clerget, MS
Elalouf, JM
Germain, G
机构
[1] INRA, Ctr Rech Jouy En Josas, Lab Neurobiol Fonct Vegetat, F-78352 Jouy En Josas, France
[2] CEA Saclay, Serv Biol Cellulaire, Dept Biol Cellulaire & Mol, F-91191 Gif Sur Yvette, France
关键词
quantitative reverse transcription-polymerase chain reaction; oxytocin receptors; vasopressin receptors; rat uterus; gestation;
D O I
10.1016/S0303-7207(97)00218-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Oxytocin receptors (OT-R) are known to be involved in the course of labor since a massive increase in OT-binding sites is observed in the uterus just before parturition. Vasopressin (AVP)-binding sites have also been observed and have been shown to mediate uterotonic responses. To determine exactly which subtypes of OT/AVP receptors are expressed in the rat uterus near parturition, we carried out absolute quantitations of the neurohypophysial hormone receptor (OT-R and the vasopressin receptors V-1a-R, V-1b-R and V-2-R) mRNAs with an assay based on reverse transcription-polymerase chain reaction (RT-PCR) using in vitro transcribed mutated cRNAs as internal standards. The number of mRNA molecules/ng of total RNA was 35 +/- 6, 220 +/- 33 and 39 +/- 9 for OT-R (P < 0.01) and 16 +/- 1, 25 +/- 8 and 31 +/- 5 for V-1a-R (P > 0.05) on day (D) 21, 22 and 23 of gestation (post-parturient), respectively. We did not detect V-1b-R and V-2-R mRNAs in the pregnant uterus. Therefore, the heterogeneity of OT and AVP receptors in the rat uterus can only be assigned to the presence of OT-R and V-1a-R neurohypophysial hormone receptor subtypes, whereas V-1b-R and V-2-R can not be invoked. Only OT-R mRNA levels change in the uterus near parturition. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:79 / 89
页数:11
相关论文
共 50 条
  • [31] Selection of internal reference gene for normalization of reverse transcription-quantitative polymerase chain reaction analysis in Mycoplasma hyopneumoniae
    Li, Shiyang
    Zhou, Yanqing
    Yuan, Ting
    Feng, Zhixin
    Zhang, Zhenzhen
    Wu, Yuzi
    Xie, Qingyun
    Wang, Jia
    Li, Quan
    Deng, Zhibang
    Yu, Yanfei
    Yuan, Xiaomin
    FRONTIERS IN VETERINARY SCIENCE, 2022, 9
  • [32] Comparison of reverse transcription-quantitative polymerase chain reaction methods and platforms for single cell gene expression analysis
    Fox, Bridget C.
    Devonshire, Alison S.
    Baradez, Marc-Olivier
    Marshall, Damian
    Foy, Carole A.
    ANALYTICAL BIOCHEMISTRY, 2012, 427 (02) : 178 - 186
  • [33] Simultaneous quantitation of cytokine mRNAs by reverse transcription-polymerase chain reaction using multiple internal standard cRNAs
    Alms, WJ
    BraunElwert, L
    James, SP
    Yurovsky, VV
    White, B
    DIAGNOSTIC MOLECULAR PATHOLOGY, 1996, 5 (02) : 88 - 97
  • [34] Reverse transcription-polymerase chain reaction products of alternatively spliced mRNAs form DNA heteroduplexes and heteroduplex complexes
    Eckhart, L
    Ban, J
    Ballaun, C
    Weninger, W
    Tschachler, E
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (05) : 2613 - 2615
  • [36] DIFFERENT LOCALIZATION AND REGULATION OF 2 TYPES OF VASOPRESSIN RECEPTOR MESSENGER-RNA IN MICRODISSECTED RAT NEPHRON SEGMENTS USING REVERSE TRANSCRIPTION-POLYMERASE CHAIN-REACTION
    TERADA, Y
    TOMITA, K
    NONOGUCHI, H
    YANG, TX
    MARUMO, F
    JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (05): : 2339 - 2345
  • [37] Differentiation of poaceae potyviruses by reverse transcription-polymerase chain reaction and restriction analysis
    Marie-Jeanne, V
    Ioos, R
    Peyre, J
    Alliot, B
    Signoret, P
    JOURNAL OF PHYTOPATHOLOGY, 2000, 148 (03) : 141 - 151
  • [38] Equivalence test in quantitative reverse transcription polymerase chain reaction:: confirmation of reference genes suitable for normalization
    Haller, F
    Kulle, B
    Schwager, S
    Gunawan, B
    von Heydebreck, A
    Sültmann, H
    Füzesi, L
    ANALYTICAL BIOCHEMISTRY, 2004, 335 (01) : 1 - 9
  • [39] Quantitative sense-specific determination of murine coronavirus RNA by reverse transcription polymerase chain reaction
    Schoenike, B
    Franta, AK
    Fleming, JO
    JOURNAL OF VIROLOGICAL METHODS, 1999, 78 (1-2) : 35 - 49
  • [40] Evaluation of synovial cytokine patterns in rheumatoid arthritis and osteoarthritis by quantitative reverse transcription polymerase chain reaction
    Wagner, S
    Fritz, P
    Einsele, H
    Sell, S
    Saal, JG
    RHEUMATOLOGY INTERNATIONAL, 1997, 16 (05) : 191 - 196