Quantification of inhibin/activin alpha and betaA subunit messenger ribonucleic acid by competitive reverse transcription-polymerase chain reaction in chicken granulosa cells during follicular development.

Abstract

The very sensitive quantitative competitive reverse transcription-polymerase chain reaction (RT-PCR) was used to investigate the expression of inhibin/activin subunits in the granulosa cells of developing ovarian follicles of the hen. Two competitors specific to inhibin alpha and betaA subunits were constructed. In one study, the expression of inhibin alpha and betaA genes was determined in the granulosa cells of the five largest yellow follicles (F1, F2, F3, F4/5), the small yellow follicles (SYF), and the large white follicles (LWF) of a layer strain of chickens. Competitive RT-PCR for inhibin alpha subunit revealed 10.35 +/- 2.15 pg/ microg total RNA in the LWF. The expression increased 40-fold in the SYF and remained at that level in the F4/5 but decreased markedly thereafter up to the F1 stage. Inhibin/activin betaA subunit was also detected in the LWF in low amounts and showed no significant increase until the F2 stage. The highest level was found in the F1. The pattern of the mRNA for alpha and betaA subunits in the five largest follicles (F1, F2, F3, F4/5) of a broiler breeder strain of chicken was compared with that in the layer strain. Expression of the alpha subunit was significantly higher in the three largest follicles (F1, F2, F3) of the broiler breeder hens, but only in the F2 for the betaA. The results suggest that inhibin alpha may play an important role in the recruitment and differentiation of follicles and that differences between broiler breeders and layers may have consequences at both the pituitary and ovarian levels.