Temporal regulation of the expression of Syncytin (HERV-W), maternally imprinted PEG10, and SGCE in human placental

被引:71
作者
Smallwood, A
Papageorghiou, A
Nicolaides, K
Alley, MKR
Jim, A
Nargund, G
Ojha, K
Campbell, S
Banerjee, S
机构
[1] Kings Coll Hosp London, Sch Med, Harris Birthright Res Ctr Fetal Med, London SE5 9RS, England
[2] Univ London Imperial Coll Sci Technol & Med, Dept Biol Sci, London SW7 2AY, England
[3] St George Hosp, Sch Med, Dept Cellular Pathol, London SW17 0RE, England
[4] St George Hosp, Sch Med, Dept Obstet, London SW17 0RE, England
[5] St George Hosp, Sch Med, Dept Gynaecol, London SW17 0RE, England
关键词
gene regulation; placenta; pregnancy; syncytiotrophoblast; trophoblast;
D O I
10.1095/biolreprod.102.013078
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Maternally imprinted PEG10 and SGCE, separated by similar to2.15 Mb from Syncytin (HERV-W) gene at 7q21.3, are implicated in choriocarcinoma and Silver-Russell syndrome. Here we have analyzed the temporal regulation of mRNA expression of these genes in placenta and demonstrate that Syncytin gene activation is highest in term placenta, PEG10, downregulated at early hypoxic phase, and highly activated at 11-12 wk of gestation. In contrast, transcription from SGCE remained unchanged throughout pregnancy, suggesting two neighboring imprinted genes are differentially regulated at very early pregnancy. Additionally, accumulation of two major species of mRNA (8 kb and 3.1 kb) encoded by HERV-Win placenta is regulated: 3.1 kb mRNA level remained unchanged throughout pregnancy, whereas the production of 8 kb species was highest in term placenta. Western blot and immunohistochemical staining of placental tissues with monoclonal antibodies revealed a marked reduction of syncytin glycoprotein synthesis in late pregnancy. Therefore, the relative levels of 3.1 kb and 8 kb mRNAs in trophoblasts could regulate syncytin protein synthesis, possibly by competition of the two mRNA species for translational apparatus.
引用
收藏
页码:286 / 293
页数:8
相关论文
共 36 条
[1]   Comparative genomic hybridization studies in hydatidiform moles and choriocarcinoma: Amplification of 7q21-q31 and loss of 8p12-p21 in choriocarcinoma [J].
Ahmed, MN ;
Kim, K ;
Haddad, B ;
Berchuck, A ;
Qumsiyeh, MB .
CANCER GENETICS AND CYTOGENETICS, 2000, 116 (01) :10-15
[2]   Embryonic inheritance of the chromatin organisation of the imprinted H19 domain in mouse spermatozoa [J].
Banerjee, S ;
Singh, PB ;
Rasberry, C ;
Cattanach, BM .
MECHANISMS OF DEVELOPMENT, 2000, 90 (02) :217-226
[3]   Placental morphogenesis in pregnancies with Down's syndrome might provide a clue to pre-eclampsia [J].
Banerjee, S ;
Smallwood, A ;
Nargund, G ;
Campbell, S .
PLACENTA, 2002, 23 (2-3) :172-174
[4]   Does blastocyst culture eliminate paternal chromosomal defects and select good embryos? Inheritance of an abnormal paternal genome following ICSI [J].
Banerjee, S ;
Lamond, S ;
McMahon, A ;
Campbell, S ;
Nargund, G .
HUMAN REPRODUCTION, 2000, 15 (12) :2455-2459
[5]   A CHROMATIN MODEL OF IGF2/H19 IMPRINTING [J].
BANERJEE, S ;
SMALLWOOD, A .
NATURE GENETICS, 1995, 11 (03) :237-238
[6]  
BEECHEY CV, 2002, GENETIC PHYSICAL IMP
[7]   An envelope glycoprotein of the human endogenous retrovirus HERV-W is expressed in the human placenta and fuses cells expressing the type D mammalian retrovirus receptor [J].
Blond, JL ;
Lavillette, D ;
Cheynet, V ;
Bouton, O ;
Oriol, G ;
Chapel-Fernandes, S ;
Mandrand, B ;
Mallet, F ;
Cosset, FL .
JOURNAL OF VIROLOGY, 2000, 74 (07) :3321-3329
[8]   Vascular endothelial growth factor and placenta growth concentrations in Down's syndrome and control pregnancies [J].
Debieve, F ;
Moiset, A ;
Thomas, K ;
Pampfer, S ;
Hubinont, C .
MOLECULAR HUMAN REPRODUCTION, 2001, 7 (08) :765-770
[9]   Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy [J].
Eggermann, T ;
Wollmann, HA ;
Kuner, R ;
Eggermann, K ;
Enders, H ;
Kaiser, P ;
Ranke, MB .
HUMAN GENETICS, 1997, 100 (3-4) :415-419
[10]   Overexpression of copper zinc superoxide dismutase impairs human trophoblast cell fusion and differentiation [J].
Frendo, JL ;
Thérond, P ;
Bird, T ;
Massin, N ;
Muller, F ;
Guibourdenche, J ;
Luton, D ;
Vidaud, M ;
Anderson, WB ;
Evain-Brion, D .
ENDOCRINOLOGY, 2001, 142 (08) :3638-3648