Jm. Rey et al., EXPRESSION OF ESTROGEN RECEPTOR-ALPHA SPLICING VARIANTS AND ESTROGEN RECEPTOR-BETA IN ENDOMETRIUM OF INFERTILE PATIENTS, Molecular human reproduction (Print), 4(7), 1998, pp. 641-647
Endometrium is one of the main target tissues of oestrogens. Although
homozygous inactivation of oestrogen receptor-alpha leads to infertili
ty in transgenic mice, oestrogen receptor-alpha is detected in endomet
rium of patients with unexplained infertility. Oestrogen receptor-alph
a splicing variants and oestrogen receptor-beta have been studied in o
estrogen target tissues, but their expression in endometrium throughou
t the menstrual cycle and in unexplained infertility is unknown. Using
reverse transcription-polymerase chain reaction (RT-PCR), we studied
the expression of oestrogen receptor-alpha splicing variants and oestr
ogen receptor-beta in uterine biopsies from 12 patients with endometri
osis and 15 patients with unexplained infertility. A control group inc
luded 19 women who had had a previous pregnancy. Our study gave eviden
ce of exon 2, 3, 4 or 7 deleted oestrogen receptor-alpha variants co-e
xisting with the wild-type receptor. We did not find any exon 5 or 6-d
eleted variants. Exon 4 or 7-deleted variants were detected in all sam
ples. Exon 2 or 3-deleted variants were detected at a similar frequenc
y in fertile women (58 and 68% respectively), endometriotic patients (
67 and 83% respectively) and infertile patients (73 and 80% respective
ly). During the follicular phase, there was a non-significant trend to
wards a lower frequency of exon-2 deleted variants in the fertile grou
p when compared with the hypofertile group. Oestrogen receptor-beta wa
s detected in all samples. Our preliminary study showed that altered e
xpression of oestrogen receptor-alpha variants and oestrogen receptor-
beta may not explain the hypofertility state.