视蛋白
生物
视黄醇X受体
视网膜
细胞生物学
受体
感光色素
甲状腺激素受体
核受体
解剖
转录因子
神经科学
遗传学
基因
生物化学
视网膜
视紫红质
作者
Melanie R. Roberts,Anita E. Hendrickson,Christopher Roger McGuire,Thomas A. Reh
摘要
purpose. The retinoid X receptors (RXRs) are members of the family of ligand-dependent nuclear hormone receptors. One of these genes, RXRγ, is expressed in highly restricted regions of the developing central nervous system (CNS), including the retina. Although previous studies have localized RXRγ to developing cone photoreceptors in several species, its function in these cells is unknown. A prior study showed that thyroid hormone receptor β2 (TRβ2) is necessary to establish proper cone patterning in mice by activating medium-wavelength (M) cone opsin and suppressing short-wavelength (S) cone opsin. Thyroid hormone receptors often regulate gene transcription as heterodimeric complexes with RXRs. methods. To determine whether RXRγ cooperates with TRβ2 to regulate cone opsin patterning, the developmental expression of RXRγ was examined, and cone opsin expression in RXRγ-null mice was analyzed. results. RXRγ was expressed in postmitotic cones and was transiently downregulated at the time of S-opsin onset in both mouse and human cones. RXRγ-null mice expressed S-opsin in all cones, similar to the TRβ2-null mice. Unlike TRβ2-null mice, which did not express M-opsin, RXRγ-null mice had a normal pattern of M-opsin expression. conclusions. RXRγ is essential (along with TRβ2) for suppressing S-opsin in all immature cones and in dorsal cones in the mature retina, but it is not necessary for M-opsin regulation. These results demonstrate a critical role for RXRs in regulating cell differentiation in the CNS and highlight a remarkable conservation of opsin regulation from Drosophila to mammals.
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