Alternative splicing of the human luteal LH receptor during luteolysis and maternal recognition of pregnancy
Deletion of exon 10 of the human LH receptor impairs LH but not hCG action. Other splice variants of the LH receptor impair both LH and hCG action in other species. We hypothesized that alternatively spliced LH receptors are involved in luteolysis and luteal rescue with hCG in women. mRNA was extrac...
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Published in: | Molecular human reproduction Vol. 10; no. 8; pp. 599 - 603 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Oxford
Oxford University Press
01-08-2004
Oxford Publishing Limited (England) |
Subjects: | |
Online Access: | Get full text |
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Summary: | Deletion of exon 10 of the human LH receptor impairs LH but not hCG action. Other splice variants of the LH receptor impair both LH and hCG action in other species. We hypothesized that alternatively spliced LH receptors are involved in luteolysis and luteal rescue with hCG in women. mRNA was extracted from human luteinized granulosa cells and from corpora lutea from across the luteal phase and after luteal rescue in vivo with exogenous hCG. Splice variants were detected by RT–PCR using carefully designed primer pairs. Products were visualized on agarose gels, extracted, purified and sequenced. Three splice variants of the human LH receptor were detected and characterized. These demonstrate a region of multiple splicing between exons 8 and 11 of the receptor. A naturally occurring splice variant with exon 10 alone removed was not identified. There was no obvious change in the pattern of splice variants across the luteal phase in the presence or absence of hCG. These data do not support the hypothesis that qualitative changes in LH receptor splicing have a role in luteolysis or that a naturally occurring LH receptor lacking exon 10 has a role in maternal recognition of pregnancy. |
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Bibliography: | 3To whom correspondence should be addressed at: Obstetrics and Gynaecology, Department of Reproductive and Developmental Sciences, University of Edinburgh, Royal Infirmary of Edinburgh – Little France, 49 Little France Crescent, Old Dalkeith Road, Edinburgh EH16 4SB, UK. Email: W.C.Duncan@ed.ac.uk local:gah076 ark:/67375/HXZ-K6B1DD8W-C istex:00B002F662EF5D1EDFA65C88FCDE70541D2B1CCD ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1360-9947 1460-2407 1460-2407 |
DOI: | 10.1093/molehr/gah076 |