Reconstituted U1 small nuclear ribonucleoprotein complex restores 5′ splice site cleavage activity Academic Article Article uri icon

Overview

MeSH Major

  • Echocardiography
  • Electrocardiography
  • Electroconvulsive Therapy
  • Mood Disorders
  • Myocardial Contraction

abstract

  • Functional reconstitution of U1 small nuclear ribonucleoprotein particle (U1 snRNP) was performed using in vitro transcribed U1 snRNA. Hela cell nuclear extract was depleted of its constituent snRNPs by centrifugation at 100,000 X g. The supernatant was devoid of snRNAs and lacked cleavage activity in splicing reactions using in vitro transcribed beta-globin pre-mRNA as substrate. The resulting pellet which contained the snRNAs, retained 5' splice site cleavage activity in a similar splicing reaction. Supplementation of the inactive supernatant fraction with in vitro transcribed U1 snRNA, partially restored 5' splice site cleavage activity thereby demonstrating the specific requirement of U1 snRNP in the initial stage of pre-mRNA splicing.

publication date

  • August 15, 1988

Research

keywords

  • Academic Article

Identity

Digital Object Identifier (DOI)

  • 10.1016/0006-291X(88)90240-9

PubMed ID

  • 2970258

Additional Document Info

start page

  • 1010

end page

  • 7

volume

  • 154

number

  • 3