Literature DB >> 1533223

The gene encoding the small nuclear ribonucleoprotein-associated protein N is expressed at high levels in neurons.

C Schmauss1, M L Brines, M R Lerner.   

Abstract

The highly homologous small nuclear ribonucleoprotein-associated proteins of the Sm group, human N and B/B', are derived from distinct, but similar genes. While the almost identical structural organization of the genes for N and B/B' suggests that they emerged from a common ancestral gene via a duplication event, they now reside on different chromosomes. In contrast to B (which is expressed in all tissues examined) and B' (which is widely expressed with the notable exception of the brain), results from in situ hybridization experiments showed that N is found predominantly in central neurons. Analysis of the transcriptional activity of the 5'-flanking sequences of the human N-encoded gene suggests that the cell-specific expression of N is achieved by selective repression of transcription by distal 5'-flanking sequences.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1533223

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  17 in total

1.  Sequencing and functional analysis of the SNRPN promoter: in vitro methylation abolishes promoter activity.

Authors:  A H Huq; J S Sutcliffe; M Nakao; Y Shen; R A Gibbs; A L Beaudet
Journal:  Genome Res       Date:  1997-06       Impact factor: 9.043

2.  The snRNP core protein SmB and tissue-specific SmN protein are differentially distributed between snRNP particles.

Authors:  J D Huntriss; D S Latchman; D G Williams
Journal:  Nucleic Acids Res       Date:  1993-08-25       Impact factor: 16.971

3.  Ubiquitous expression and imprinting of Snrpn in the mouse.

Authors:  J A Barr; J Jones; P H Glenister; B M Cattanach
Journal:  Mamm Genome       Date:  1995-06       Impact factor: 2.957

4.  Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient.

Authors:  Y Sun; R D Nicholls; M G Butler; S Saitoh; B E Hainline; C G Palmer
Journal:  Hum Mol Genet       Date:  1996-04       Impact factor: 6.150

5.  Imprinting-mutation mechanisms in Prader-Willi syndrome.

Authors:  T Ohta; T A Gray; P K Rogan; K Buiting; J M Gabriel; S Saitoh; B Muralidhar; B Bilienska; M Krajewska-Walasek; D J Driscoll; B Horsthemke; M G Butler; R D Nicholls
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

6.  Porcine circovirus type 2 ORF4 protein binds heavy chain ferritin.

Authors:  Qizhuang Lv; Kangkang Guo; Tao Wang; Chengcheng Zhang; Yanming Zhang
Journal:  J Biosci       Date:  2015-09       Impact factor: 1.826

7.  Mice lacking dopamine D2 and D3 receptors have spatial working memory deficits.

Authors:  Sara B Glickstein; Patrick R Hof; Claudia Schmauss
Journal:  J Neurosci       Date:  2002-07-01       Impact factor: 6.167

8.  Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.

Authors:  C C Glenn; S Saitoh; M T Jong; M M Filbrandt; U Surti; D J Driscoll; R D Nicholls
Journal:  Am J Hum Genet       Date:  1996-02       Impact factor: 11.025

9.  An imprinted, mammalian bicistronic transcript encodes two independent proteins.

Authors:  T A Gray; S Saitoh; R D Nicholls
Journal:  Proc Natl Acad Sci U S A       Date:  1999-05-11       Impact factor: 11.205

10.  Isoforms of U1-70k control subunit dynamics in the human spliceosomal U1 snRNP.

Authors:  Helena Hernández; Olga V Makarova; Evgeny M Makarov; Nina Morgner; Yutaka Muto; Daniel Pomeranz Krummel; Carol V Robinson
Journal:  PLoS One       Date:  2009-09-28       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.