Identification of nuclear proteins that are developmentally regulated in embryonic rat brain

• Published in: Journal of neurochemistry Vol. 64; no. 5; p. 1919
• Main Authors: Thormodsson, F R, Redmond, L, Hockfield, S
• Format: Journal Article
• Language: English
• Published: England 01.05.1995
• Subjects: Animals; Brain - embryology; Brain - metabolism; Brain - ultrastructure; Cell Fractionation; Cell Nucleus - chemistry; Electrophoresis, Gel, Two-Dimensional; Female; Fluorometry; Image Processing, Computer-Assisted; Liver - embryology; Liver - metabolism; Liver - ultrastructure; Nerve Tissue Proteins - analysis; Nerve Tissue Proteins - metabolism; Nuclear Proteins - analysis; Nuclear Proteins - metabolism; Pregnancy; Rats; Rats, Sprague-Dawley
• ISSN: 0022-3042
• DOI: 10.1046/j.1471-4159.1995.64051919.x

To identify nuclear proteins that might play a role in the acquisition of neuronal phenotype, two-dimensional polyacrylamide gel electrophoresis (2D-PAGE) was used to analyze nuclear proteins expressed over the course of embryonic rat brain development. Metabolically labeled rat brain nuclear proteins from embryonic day 14 (E14) were compared with proteins from embryonic day 20 (E20). Over this period, the rat brain develops from a collection of relatively homogeneous precursor cells into a complex structure containing many different classes of neurons. Computer-assisted analysis of 2D-PAGE fluorograms identified 11 proteins that show increases in their rate of synthesis between E14 and E20. Twenty proteins that consistently appear at E20 are not detectable on fluorograms of E14 nuclear proteins, even after long exposures, and thus may be considered to appear de novo. Fifty-eight proteins show consistent down-regulation between E14 and E20, and of these, 19 are not detectable on fluorograms of E20 nuclear proteins. The electrophoretic properties of many of these proteins suggest that they are previously unreported, developmentally regulated nuclear proteins. Some of the developmentally regulated, brain-enriched nuclear proteins identified here may play a role in regulating the expression of neural genes important for cellular differentiation in the mammalian CNS.