학술논문

LIM-homeodomain proteins Lhxl and Lhx5, and their cofactor Ldb1, control Purkinje cell differentiation in the developing cerebellum
NEUROSCIENCE
Document Type
Clinical report
Source
Proceedings of the National Academy of Sciences of the United States. August 7, 2007, Vol. 104 Issue 32, p13182, 5 p.
Subject
United States
Language
English
ISSN
0027-8424
Abstract
Purkinje cells are one of the major types of neurons that form the neural circuitry in the cerebellum essential for fine control of movement and posture. During development, Purkinje cells also are critically involved in the regulation of proliferation of progenitors of granule cells, the other major type of neurons in the cerebellum. The process that controls differentiation of Purkinje cells from their early precursors is poorly understood. Here we report that two closely related LIM-homeobox genes, Lhx1 and Lhx5, were expressed in the developing Purkinje cells soon after they exited the cell cycle and migrated out of the cerebellar ventricular zone. Double-mutant mice lacking function of both Lhx1 and Lhx5 showed a severe reduction in the number of Purkinje cells. In addition, targeted inactivation of Ldb1, which encodes a cofactor for all LIM-homeodomain proteins, resulted in a similar phenotype. Our studies thus provide evidence that these transcription regulators are essential for controlling Purkinje cell differentiation in the developing mammalian cerebellum. CNS | development | embryo | mouse | transcription