Skip Navigation


Hum. Reprod. Advance Access originally published online on August 25, 2005
Human Reproduction 2005 20(12):3360-3368; doi:10.1093/humrep/dei261
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF ) Freely available
Right arrow All Versions of this Article:
20/12/3360    most recent
dei261v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (4)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Rull, K.
Right arrow Articles by Laan, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rull, K.
Right arrow Articles by Laan, M.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author 2005. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oupjournals.org

Expression of {beta}-subunit of HCG genes during normal and failed pregnancy

Kristiina Rull1,2,3 and Maris Laan2

1 Department of Obstetrics and Gynecology, University of Tartu and 2 Department of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia

3 To whom correspondence should be addressed: Department of Obstetrics and Gynecology, University of Tartu, Lossi 36, Tartu, 51003 Estonia. E-mail: Kristiina.Rull{at}kliinikum.ee

BACKGROUND: One of the first proteins synthesized by a conceptus is HCG. The receptor-binding {beta}-subunit of HCG (HCG{beta}) is encoded by highly homologous CGB, CGB5, CGB7 and CGB8 genes. The function of two additional gene copies, CGB1 and CGB2, is still unknown. We aimed to compare the expression of individual CGB genes during normal pregnancy and in cases of recurrent miscarriage (RM) and ectopic pregnancy (EP). METHODS: A semiquantitative RT–PCR with fluorescent-labelled primers coupled with the gene-specific restriction and quantification was used. RESULTS: The summarized expression of HCG{beta} genes was high throughout the pregnancy, and moderately correlated with HCG in serum. In cases of RM, reduced hormone values were consistent with low mRNA levels, whereas for EP no reduction in transcriptional activity was detected. CGB1and CGB2 showed a considerable expression peak during the first trimester, both in normal and ectopic pregnancy, but not for RM. CONCLUSIONS: In cases of RM, low HCG could result from expression failure of HCG{beta} genes, whereas in EP the problems other than the transcriptional failure contribute to reduced hormone levels. The expression patterns of CGB1 and CGB2 suggest their putative role in the implantation stage.

Key words: CGB gene expression/ectopic pregnancy/HCG/implantation/recurrent miscarriage


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Mol Hum ReprodHome page
K. Rull, P. Hallast, L. Uuskula, J. Jackson, M. Punab, A. Salumets, R.K. Campbell, and M. Laan
Fine-scale quantification of HCG beta gene transcription in human trophoblastic and non-malignant non-trophoblastic tissues
Mol. Hum. Reprod., January 1, 2008; 14(1): 23 - 31.
[Abstract] [Full Text] [PDF]


Home page
LupusHome page
N Schwartz, Y Shoenfeld, O Barzilai, R Cervera, J Font, M Blank, S Yacobi, N Patlas, A Cohen, D Mevorach, et al.
Reduced placental growth and hCG secretion in vitro induced by antiphospholipid antibodies but not by anti-Ro or anti-La: studies on sera from women with SLE/PAPS
Lupus, February 1, 2007; 16(2): 110 - 120.
[Abstract] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.