Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1989 Dec;9(12):5273-80.
doi: 10.1128/mcb.9.12.5273-5280.1989.

Multiple splicing factors are released from endogenous complexes during in vitro pre-mRNA splicing

Affiliations

Multiple splicing factors are released from endogenous complexes during in vitro pre-mRNA splicing

G C Conway et al. Mol Cell Biol. 1989 Dec.

Abstract

Pre-mRNA splicing occurs in a macromolecular complex called the spliceosome. Efforts to isolate spliceosomes from in vitro splicing reactions have been hampered by the presence of endogenous complexes that copurify with de novo spliceosomes formed on added pre-mRNA. We have found that removal of these large complexes from nuclear extracts prevents the splicing of exogenously added pre-mRNA. We therefore examined these complexes for the presence of splicing factors and proteins known or thought to be involved in RNA splicing. These fast-sedimenting structures were found to contain multiple small nuclear ribonucleoproteins (snRNPs) and a fragmented heterogeneous nuclear ribonucleoprotein complex. At least two splicing factors other than the snRNPs were also associated with these large structures. Upon incubation with ATP, these splicing factors as well as U1 and U2 snRNPs were released from these complexes. The presence of multiple splicing factors suggests that these complexes may be endogenous spliceosomes released from nuclei during preparation of splicing extracts. The removal of these structures from extracts that had been preincubated with ATP yielded a splicing extract devoid of large structures. This extract should prove useful in the fractionation of splicing factors and the isolation of native spliceosomes formed on exogenously added pre-mRNA.

PubMed Disclaimer

References

    1. Cell. 1983 Jun;33(2):509-18 - PubMed
    1. J Biol Chem. 1983 Jun 10;258(11):7181-9 - PubMed
    1. Cell. 1983 Nov;35(1):101-7 - PubMed
    1. EMBO J. 1983;2(7):1129-35 - PubMed
    1. Biol Cell. 1983;49(1):1-10 - PubMed

Publication types

MeSH terms

LinkOut - more resources