Identification and characterization of BC1 RNP particles

被引:45
作者
Cheng, JG
Tiedge, H
Brosius, J
机构
[1] UNIV MUNSTER, CTR MOL BIOL INFLAMMAT, INST EXPT PATHOL, D-48149 MUNSTER, GERMANY
[2] MT SINAI SCH MED, FISHBERG RES CTR NEUROBIOL, NEW YORK, NY 10029 USA
[3] MT SINAI SCH MED, BROOKDALE CTR MOL BIOL, NEW YORK, NY 10029 USA
[4] SUNY HLTH SCI CTR, DEPT PHARMACOL, BROOKLYN, NY 11203 USA
[5] SUNY HLTH SCI CTR, DEPT NEUROL, BROOKLYN, NY 11203 USA
关键词
D O I
10.1089/dna.1996.15.549
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Rodent brain-specific small cytoplasmic BC1 RNA is an unusual RNA in several respects, It is an RNA polymerase III transcript expressed specifically in neurons, with regional and developmental regulation, Moreover, it is one of a few RNAs actively transported into dendrites, Three findings indicate that BC1 RNA exists as a ribonucleoprotein complex in vivo. First, the buoyant density of fractions containing BC1 RNA from brain extract on CsCl and Cs2SO4 gradients is 1.45 g/ml and 1.55 g/ml, respectively; this is consistent with the density of RNA-protein complexes, Second, in sucrose gradients, the BC1 particle has a larger S value (8.7S) than naked RNA (6.1S). Third, BC1 RNA from brain extracts migrates with retarded mobility compared to naked BC1 RNA during agarose gel electrophoresis. Additionally, in comparison to the signal recognition particle (SRP), the BC1 RNP is more heat resistant and less Mg2+-dependent. The buoyant density of the BC1 RNP suggests the presence of protein(s) with a total mass of about 138kD.
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页码:549 / 559
页数:11
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