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
. 1994 Nov;127(3):593-607.
doi: 10.1083/jcb.127.3.593.

Association of nuclear matrix antigens with exon-containing splicing complexes

Affiliations

Association of nuclear matrix antigens with exon-containing splicing complexes

B J Blencowe et al. J Cell Biol. 1994 Nov.

Abstract

mAbs raised against the human nuclear matrix (anti-NM)1 mAbs have been used to investigate the role of nuclear matrix antigens in pre-mRNA processing. The three anti-NM mAbs used in this study recognize antigens that are highly localized to nuclear matrix speckles. Surprisingly, all three of these mAbs preferentially immunoprecipitate splicing complexes containing exon sequences. The anti-NM mAbs efficiently immunoprecipitate the exon product complex but not complexes containing the lariat product after the second step of splicing. Two of the anti-NM mAbs completely inhibit pre-mRNA splicing in vitro. However, none of the anti-NM mAbs appear to recognize factors stably associated with splicing snRNPs. The three anti-NM mAbs predominantly react with distinct high molecular weight antigens, which belong to a class of nuclear proteins that selectively precipitate with Ser-Arg protein-splicing factors in the presence of high Mg2+ concentrations. Immunological, biochemical, and cell biological data indicate that two of the NM antigens are related to the defined set of Ser-Arg proteins. The results suggest the existence of an extended Ser-Arg family as a component of the nuclear matrix.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Cell Biol. 1978 Mar;76(3):675-91 - PubMed
    1. Genes Dev. 1987 Aug;1(6):532-43 - PubMed
    1. Cell. 1991 May 17;65(4):579-86 - PubMed
    1. J Cell Biol. 1990 Mar;110(3):569-80 - PubMed
    1. Cell. 1993 Jul 16;74(1):105-14 - PubMed

Publication types

MeSH terms