Xenbase Image ID: 153343
Fig. 2. Tissue distribution of mRNAs for corticotropin-releasing factor system components in juvenile Xenopus laevis tissues analyzed by RT-PCR. RNA
isolation and RT-PCR is described by Boorse et al. (2005a) and the PCR primer sequences are given in Table 1. (A) Expression analysis in brain and pituitary.
(B) Expression analysis in diverse peripheral tissues. Corticotropin-releasing factor (CRF), urocortin 1 (UCN1), urocortin 3 (UCN3), CRF binding
protein (CRF-BP), CRF receptor 1 (CRF1) and CRF receptor 2 (CRF2). Ribosomal L8 (rpL8) was used as a housekeeping gene to control for RNA quality
and loading. Shown are representative ethidium bromide-stained gels of RT-PCR products; RNA was harvested from tissues of three females and similar
results were obtained with each. PCR reactions conducted on reverse transcription reactions in which the reverse transcriptase was omitted (minus RT
reactions) produced no bands, thus conWrming the absence of genomic DNA contamination + and ¡ on the Wgure. RT-PCR reactions conducted on RNA
isolated from whole blood or packed blood cells produced no bands, which shows that the positive results that we obtained in other tissues are not due to
contamination from blood cells. However, we cannot rule out the possibility that some blood cell types express CRF system signaling components but
their abundance was below the level of detection of our assay.
Image published in: Boorse GC and Denver RJ (2006)
Copyright © 2006. This image is reproduced with permission of the publisher and the copyright holder. This is an Open Access article distributed under the terms of the Creative Commons Attribution License.
Image source: Published
Printer Friendly View