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Little is known of transcriptional mechanisms underlying the development of the trigeminal (V) principal sensory nucleus (PrV), the brainstem nucleus responsible for the development of the whisker-to-barrel cortex pathway. Lmx1b, a LIM homeodomain transcription factor, is expressed in embryonic PrV. In Lmx1b knockout ((-)(/)(-)) mice, V primary afferent projections to PrV are normal, albeit reduced in number, whereas the PrV-thalamic lemniscal pathway is sparse and develops late. Excess cell death occurs in the embryonic Lmx1b(-)(/)(-) PrV, but not in Lmx1b/Bax double null mutants. Expression of Drg11, a downstream transcription factor essential for PrV development and pattern formation, is abolished in PrV, but not in the V ganglion. Consequently, whisker patterns fail to develop in PrV by birth. Rescued PrV cells in Lmx1b/Bax double (-)(/)(-)s failed to rescue whisker-related PrV pattern formation. Thus, Lmx1b and Drg11 may act in the same genetic signaling pathway that is essential for PrV pattern formation.
Homeodomain Proteins, Mice, Knockout, Afferent Pathways, Cell Death, LIM-Homeodomain Proteins, Nerve Tissue Proteins, Trigeminal Nuclei, Mice, Inbred C57BL, Mice, Animals, Newborn, Thalamus, Trigeminal Ganglion, Vibrissae, Animals, Body Patterning, Transcription Factors, bcl-2-Associated X Protein
Homeodomain Proteins, Mice, Knockout, Afferent Pathways, Cell Death, LIM-Homeodomain Proteins, Nerve Tissue Proteins, Trigeminal Nuclei, Mice, Inbred C57BL, Mice, Animals, Newborn, Thalamus, Trigeminal Ganglion, Vibrissae, Animals, Body Patterning, Transcription Factors, bcl-2-Associated X Protein
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