Hormonal and Molecular Regulation of the Cytochrome P450 Aromatase Gene Expression in the Ovary

2009 ◽  
pp. 257-269 ◽  
Author(s):  
Carlos Stocco
2013 ◽  
Vol 34 (5) ◽  
pp. 480-488 ◽  
Author(s):  
William J. Trickler ◽  
Xiaoqing Guo ◽  
Elvis Cuevas ◽  
Syed F. Ali ◽  
Merle G. Paule ◽  
...  

2014 ◽  
Vol 117 (1) ◽  
pp. 66-72 ◽  
Author(s):  
B.N.V. Lakshminarayana ◽  
V. Praveen Chakravarthi ◽  
K.V. Brahmaiah ◽  
V.H. Rao

2021 ◽  
Vol 38 (2) ◽  
pp. 247-252
Author(s):  
Guler Unal ◽  
Emily Marquez ◽  
Mara H. O'brien ◽  
Pericles Stavropoulos ◽  
Ian P. Callard

In this study, we aimed to clone brain-derived Cyp19b and ovary-derived Cyp19a the P450 aromatase gene isoforms and to indicate the expression levels of these genes in the hypothalamus and ovary tissues from reproductively arrested ovarian development (RA) and non-arrested ovarian development (RN) Alburnus tarichi from Lake Van, Turkey. The expression levels of Cyp19b and Cyp19a genes were predominant in the hypothalamus and ovary, respectively. The level of Cyp19b mRNA was significantly lower in the hypothalamus and ovary from RA fish than in the hypothalamus and ovary from RN fish (P<0.05). The expression level of Cyp19a was significantly lower in the ovary of RA fish (P<0.05) than RN fish while no difference was found in the hypothalamus of both RA and RN fish (P<0.05). According to these findings, we suggest that the RA fish represent a segment of the population and these fish may be more sensitive to endocrine disruption compound/s than others.


2013 ◽  
Vol 25 (1) ◽  
pp. 234
Author(s):  
E. K. N. Arashiro ◽  
S. Wohlres-Viana ◽  
M. P. Palhao ◽  
L. S. A. Camargo ◽  
M. Henry ◽  
...  

It is well documented that the size of the dominant follicle at deviation is smaller in Bos indicus compared with in Bos taurus breeds. The physiological mechanisms underlying this difference, however, are unknown. The aim of the present study was to evaluate the dynamic of oestradiol production during follicle development close to the expected moment of deviation in Bos taurus and Bos indicus dairy heifers. Intrafollicular concentration of oestradiol (E2) and P450 aromatase gene expression in granulosa cells (GC) were evaluated in Gir (n = 10) and Holstein (n = 10) heifers. Follicular waves were synchronized with an intravaginal progesterone device (1 g, Sincrogest, Ourofino Agropecuária, São Paulo, Brazil) and benzoate oestradiol (2 mg im, Sincrodiol, Ourofino Agropecuária). Ultrasonography evaluations (MyLab30 Vet Gold, Esaote, Genova, Italy, with a 7.5-MHz transducer) were performed every 24 h to detect the emergence of the new follicular waves. The largest follicle of each wave was individually aspirated by ovum pickup before, at the expected diameter, or after deviation in both Gir (4.6 ± 0.2, 6.3 ± 0.2, and 8.5 ± 0.6 mm, respectively) and Holstein heifers (6.0 ± 0.5, 8.6 ± 0.4, and 10.2 ± 0.2 mm, respectively), as previously described (Arashiro et al. 2012 Reprod. Fertil. Dev. 24, 175). Follicular fluid (FF) samples were centrifuged and the supernatant stored at –20°C until E2 and progesterone (P4) determination by RIA. The pellet of GCs was washed twice with PBS, kept in RNAlater, and frozen at –20°C until RNA extraction and reverse transcription. Relative transcript quantification was performed by real-time PCR. The β-actin gene was used as control. Samples of FF with E2:P4 ratio <1 or presenting contamination by theca cells (detected by the expression of 17α-hydroxylase) were not used for statistical analyses. Concentration of E2 in FF was evaluated between breeds and among follicle size classes by ANOVA and differences among means compared by Student t-test or Tukey’s test, respectively. Within breeds, relative gene expression was accessed by pair-wise fixed reallocation randomization test (software REST®). Results are shown as mean ± SEM. In both breeds, concentration of E2 in FF progressively increased with follicular diameter (P < 0.05). Intrafollicular concentration of E2 (ng mL–1) was greater (P < 0.05) in Holstein than in Gir before (58.5 ± 11.7 v. 8.8 ± 2.0), at expected (226.0 ± 49.9 v. 78.9 ± 21.0), and after follicle deviation (579.1 ± 45.0 v. 185.0 ± 34.9). Interestingly, however, follicles with similar diameters (~6 or 8 mm) showed similar (P > 0.05) E2 concentrations between Holstein and Gir. Moreover, in both breeds, the relative expression of P450 aromatase gene in GC first increased (3.9 ± 2.4 and 67.5 ± 52.8 for Holstein and Gir, respectively; P < 0.05) at the same stage of follicular development (8 mm). The present results suggest that the smaller size of follicles at deviation in Bos indicus is not related to an earlier increase in intrafollicular E2 production. CNPq, CAPES, and Fapemig (CVZ APQ 02863/09).


2005 ◽  
Vol 35 (3) ◽  
pp. 571-583 ◽  
Author(s):  
Y Kazeto ◽  
J M Trant

Cytochrome P450 aromatase (CYP19) converts androgens to estrogens. Unlike mammals, teleosts have two CYP19 genes, expressed differentially in ovary (CYP19A1) and neuronal tissues (CYP19A2). The primary purpose of this study was to demonstrate the potential involvement of CYP19A2 in the reproductive endocrinology of teleosts. Channel catfish CYP19A2 (ccCYP19A2) cDNAs were isolated from the brain using a PCR-based strategy. The ccCYP19A2 cDNA putatively encodes 500 amino acids which conferred aromatase activity in transfected COS-7 cells. Additionally, an alternatively spliced transcript was isolated which lacks the first 122 amino acids and is catalytically inactive. The brain and the pituitary were predominant sources of ccCYP19A2 transcript and the abundance in both tissues acutely increased prior to spawning. This preovulatory induction of ccCYP19A2 gene in the pituitary is remarkably similar to the pattern of gene expression for luteinizing hormone-β (LHβ). Estradiol-17β (E2) and testosterone enhanced the transcript abundance of ccCYP19A2 and LHβ in catfish pituitary cells cultured in vitro but the stimulatory effects of testosterone were abolished by an aromatase inhibitor, indicating an important role of E2, the product of CYP19A2 activity, in the regulation of CYP19A2 and LHβ. Structural and functional analysis of the 5′-flanking region of the gene suggested that the sequence from −1076 to − 435 bp is critical for the basal promoter activity in the pituitary. This report demonstrates that CYP19A2 functions as an important factor in the reproductive endocrinology of teleosts through the brain-pituitary-gonadal axis.


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