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1

Expression of alpha and beta estrogen receptors in the chicken ovary

100%
Hrabia A., Wilk M., Rzasa J.
Folia Biologica
|
2008
|
vol. 56
|
issue 3-4
187-191
EN
The role of estrogens in hen reproduction is well established. However, the distribution of estrogen receptors in the chicken ovary is unknown. Therefore, the mRNA expression of alpha (ERalpha) and beta (ERbeta) estrogen receptors was examined within the ovaries of laying hens. Expression of ERs was determined by RT-PCR analysis. The presence of ERalpha and ERbeta mRNAs was found in the ovarian stroma and white, yellowish, small yellow and the largest preovulatory (F3-F1) follicles. ERalpha and ERbeta mRNAs were detected in the granulosa and theca layers of the walls of preovulatory follicles. The expression of ERalpha mRNA was markedly higher than ER? mRNA in all examined ovarian compartments. Within the ovary, the relative expression of both ER mRNAs depends on the follicular diameter and the layer of the follicular wall. The results demonstrate the expression of both ERalpha mRNA and ERbeta mRNA in all compartments of the chicken ovary, suggesting different pathways of estrogen action in the avian ovary. Much higher expression of ERalpha mRNA indicates that this form of estrogen receptor is predominant in the chicken ovary. The clarification of the mechanism of ER? and ER? participation in the ovarian functions of birds necessitates further experiments examining ERs at the protein level.
2

Relation between Ava I polymorphism within the estrogen receptor gene (ESR) and meatiness in Polish Large White boars

100%
Kaminski S., Rusc A., Brym P.
Journal of Applied Genetics
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2003
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vol. 44
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issue 4
521-524
EN
It is currently debated whether identification of ESR (estrogen receptor) genotypes should be introduced into breeding programs of Large White pigs. The aim of this study was to evaluate the possible relations between ESR/Ava I polymorphism and carcass performance traits in Polish Large White boars. We examined 103 boars originating from one herd in NE Poland. ESR/Ava I genotypes were determined by the PCR-RFLP method. By the use of the Duncan test, we found highly significant differences (P < 0.01) between WW and MW genotypes, as well as significant differences (P < 0.05) between WW and MM genotypes for meatiness. No significant differences were found for daily gain and selection index.
3

Polymorphism within the bovine estrogen receptor-a gene 5?-region

100%
Szreder T., Zwierzchowski L.
Journal of Applied Genetics
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2004
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vol. 45
|
issue 2
225-236
EN
Due to the functions that estrogens play in the regulation of reproduction, development of the mammary gland, growth and differentiation of cells, estrogen receptors and their genes are considered candidates for the markers of production and functional traits in farm animals, including cattle. In the present study, on the basis of the sequences of the human, ovine, and porcine ER genes, available in the GenBank database, sets of PCR primers were designed and used to amplify the bovine ERa gene 5?-region. Seven overlapping fragments of the 5? region of the bovine ERa gene were amplified and then sequenced. Altogether, these fragments were composed in the 2853-bp sequence which was deposited in the GenBank database under accession no. AY340597. The sequenced fragment included the noncoding exons A, B, C, their putative promoters, and a part of the coding exon 1. A polymorphism within the 5? region of the bovine ERa gene ? A/G transition, which could be recognized with RFLP-BglI, lying upstream to the exon C, was identified for the first time using this sequence.
4

Simultaneous identification of ryanodine receptor 1 (RYR1) and estrogen receptor (ESR) genotypes with the multiplex PCR-RFLP method in Polish Large White and Polish Landrace pigs

75%
Kaminska S., Rusc A., Wojtasik K.
Journal of Applied Genetics
|
2002
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vol. 43
|
issue 3
331-335
EN
A method allowing simultaneous genotyping of two loci: ryanodine receptor 1 (RYR1) and estrogen receptor (ESR) is presented. In multiplex PCR amplification, two amplicons were simultaneously produced: a 272 bp fragment of RYR1 gene and a 185 bp fragment of ESR gene and were then subjected to ?one-tube? restriction enzyme digestion with Hin6 I and Ava I, respectively. A total of 122 Polish Large White and Polish Landrace pigs were genotyped by this method, demonstrating its reliability, convenience and lower costs. This method may be useful in the wide-scale genotyping of both loci in pig breeding programmes.
5

Hormonal regulation of oestrogen formation by Leydig cells in vitro: immunocytochemical approach

75%
Gancarczyk M., Tworzydlo W., Szlachta A., Sadowska J., Bilinska B.
Folia Biologica
|
2003
|
vol. 51
|
issue 3-4
181-188
EN
The ability of the testis to convert androgens into oestrogens is related to the presence of a microsomal enzyme, aromatase, in testicular cells. The aim of this study was to show whether the supplementation of culture media with LH or an aromatase inhibitor could affect the process of aromatisation in Leydig cells of the bank vole in vitro. This was investigated by means of immunocytochemistry and radioimmunological assays. In control cultures of Leydig cells, both steroid hormones secretion as well as immunoreactivities for aromatase and oestrogen receptor were weaker than in those treated with LH. On the contrary, the addition of aromatase inhibitor into the culture medium resulted in a decreased intensity of immunocytochemical stainings in comparison with the control. Concomitantly, the androgen level was slightly higher, whereas that of oestrogen significantly lower than in the control cultures. Additionally, to check whether steroid hormones are able to regulate aromatase or oestrogen receptor immunoexpressions, some of the Leydig cell cultures were enriched with testosterone or oestradiol, respectively. Strong immunoreactivities for both aromatase and oestrogen receptor were observed. This suggests that Leydig cells in vitro are able to regulate directly the secretion of oestrogens by active aromatase. Finally, it is concluded that oestrogen formation in bank vole Leydig cells in vitro can be influenced by various factors. It should be stressed, however, that the effect of hormone stimulation or aromatase inhibitor action appeared to be dependent on the length of light cycles that bank voles were exposed prior to the isolation of Leydig cells.
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