Differential expression of vitelline membrane outer layer protein 1: Hormonal regulation of expression in the oviduct and in ovarian carcinomas from laying hens. (5th January 2015)

• Record Type: Journal Article
• Authors: Lim, Whasun; Song, Gwonhwa
• Is Part Of: Molecular and cellular endocrinology. Volume 399(2015)
• Page Start: 250
• Page End: 258
• Publication Date: 2015-01-05
• Subjects: VMO1 -- Hen -- Estrogen -- Molting -- Oviduct -- Ovarian cancer; Endocrinology -- Periodicals; Molecular biology -- Periodicals; Cytology -- Periodicals; Endocrinology -- Periodicals; Hormones -- Periodicals; Endocrinologie -- Périodiques; Cytology; Endocrinology; Molecular biology; Periodicals; 573.4
• DOI: 10.1016/j.mce.2014.10.015
• Languages: English
• ISSNs: 0303-7207

Abstract

Highlights: VMO1 is a novel estrogen-responsive gene expressed during oviductal recrudenscence. VMO1 is regulated by specific microRNAs during during the molting period. VMO1 is abundantly expressed in ovarian carcinomas of laying hens. Abstract: Vitelline membrane outer layer protein 1 (VMO1), a basic protein present in the outer layer of the vitelline membrane of eggs, plays essential roles in separating the yolk from the egg white and preventing infection from bacteria by forming a barrier of fibrous layers in avian eggs. Although VMO1 is expressed in the oviduct of hens, little is known about endocrine regulation of transcription of VMO1 in the oviduct and its expression in cancerous ovaries of laying hens. Results of present study indicated that expression of VMO1 mRNA increased in the chick oviduct in response to diethylstilbestrol (DES, a synthetic non-steroidal estrogen). VMO1 mRNA and protein were particularly abundant in the glandular epithelium (GE) and luminal epithelium (LE) of the magnum of the oviducts of chicks treated with DES. Also, during the regression and recrudescence phases of the oviduct during induced molting with zinc feeding, VMO1 expression decreased as the oviduct regressed and increased with remodeling and recrudescence of the oviduct in laying hens. In addition, changes in relative expression of specific microRNAs ( miR-1623, miR-1552-3p, miR-1573, miR-22-3p, miR-124a and miR-1764 ) regulating VMO1 gene were detected in the oviducts during the molting period. Moreover, abundant expression of VMO1 was found in GE of cancerous, but not normal ovaries of laying hens. Results of the present study suggest that VMO1 is regulated by estrogen and target microRNAs in the chicken oviduct and that it is a potential diagnostic marker of ovarian cancer in laying hens.