» Articles » PMID: 4026804

Decreased Ovalbumin-gene Response to Oestrogen in the Prenatally Diethylstilboestrol-exposed Chick Oviduct

Overview
Journal Biochem J
Specialty Biochemistry
Date 1985 Jun 15
PMID 4026804
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Prenatal exposure of the female chick-embryo Müllerian duct to diethylstilboestrol (DES) decreases its future capacity for epithelial tubular-gland-cell differentiation and oviduct ovalbumin-gene expression. Chick Müllerian ducts after prenatal exposure to different concentrations of DES were tested after birth to determine the response of the oviduct toward the oestrogen induction. The quantity of DNA was biochemically determined, the differentiation of tubular-gland cells in the oviduct was studied by light microscopy, and the expression of the ovalbumin gene was detected by hybridization of the total RNA with radioactive ovalbumin cDNA. Comparisons among these three parameters revealed that the expression of the ovalbumin gene was affected most by DES exposure. Exposure to high doses of DES suppressed ovalbumin-gene expression by 75-78%, and inhibited tubular-gland-cell differentiation and thus decreased the DNA content by 29 and 32% respectively. Exposure to low doses of DES caused suppression of ovalbumin-gene expression by 47-53%, but it did not affect the other two parameters. Prenatal DES exposure has strong inhibitory effects on the Müllerian duct at the age (5-8-day-old embryos) when the organ is undifferentiated. Less inhibition is observed when the organ becomes differentiated (15-day-old embryos and older).

Citing Articles

Masculine epigenetic sex marks of the CYP19A1/aromatase promoter in genetically male chicken embryonic gonads are resistant to estrogen-induced phenotypic sex conversion.

Ellis H, Shioda K, Rosenthal N, Coser K, Shioda T Biol Reprod. 2012; 87(1):23, 1-12.

PMID: 22539680 PMC: 3406558. DOI: 10.1095/biolreprod.112.099747.


Histological changes in the uterus of the hens after embryonic exposure to bisphenol A and diethylstilbestrol.

Yigit F, Daglioglu S Protoplasma. 2010; 247(1-2):57-63.

PMID: 20393758 DOI: 10.1007/s00709-010-0140-x.


Purification and properties of an oestrogen-stimulated mouse uterine glycoprotein (approx. 70 kDa).

TENG C, Walker M, Bhattacharyya S, Klapper D, DiAugustine R, McLachlan J Biochem J. 1986; 240(2):413-22.

PMID: 3814091 PMC: 1147433. DOI: 10.1042/bj2400413.


Lectin bindings and diethylstilbestrol effects on the recognition of mullerian inhibiting substance (MIS) on chick mullerian ducts by MIS-antiserum.

Wang J, Yin C, Teng C Histochemistry. 1990; 95(1):55-61.

PMID: 2286533 DOI: 10.1007/BF00737228.

References
1.
McLachlan J, Newbold R, Bullock B . Long-term effects on the female mouse genital tract associated with prenatal exposure to diethylstilbestrol. Cancer Res. 1980; 40(11):3988-99. View

2.
Kaufman R, Adam E, Binder G, Gerthoffer E . Upper genital tract changes and pregnancy outcome in offspring exposed in utero to diethylstilbestrol. Am J Obstet Gynecol. 1980; 137(3):299-308. DOI: 10.1016/0002-9378(80)90913-8. View

3.
LOWRY O, ROSEBROUGH N, FARR A, RANDALL R . Protein measurement with the Folin phenol reagent. J Biol Chem. 1951; 193(1):265-75. View

4.
MASTER R . POSSIBLE SYNTHESIS OF POLYRIBONUCLEOTIDES OF KNOWN BASE-TRIPLET SEQUENCES. Nature. 1965; 206:93. DOI: 10.1038/206093b0. View

5.
MUNRO H . The determination of nucleic acids. Methods Biochem Anal. 1966; 14:113-76. DOI: 10.1002/9780470110324.ch5. View