Literature DB >> 9664900

Expression of the 'dead box' RNA helicase p68 is developmentally and growth regulated and correlates with organ differentiation/maturation in the fetus.

R J Stevenson1, S J Hamilton, D E MacCallum, P A Hall, F V Fuller-Pace.   

Abstract

The human DEAD box protein p68 is an established RNA-dependent ATPase and RNA helicase, p68 has been highly conserved in evolution and appears to be essential for normal growth, suggesting that this protein plays an important role in the cell. Although the biochemical activities of p68 are fairly well characterized, little is known about its biological function. This report shows that p68 is detectable in quiescent cell lines, but its expression is induced by serum, suggesting that this protein may play a role in cell growth. It is also shown that both p68 mRNA and protein are differentially expressed in adult tissues; in this case, however, the levels do not always correlate with proliferation status, suggesting that the regulation of expression in the animal may be different from that in cell lines. Finally, it is shown that p68 expression is developmentally regulated and appears to correlate with organ differentiation/maturation. These findings suggest that p68 expression may not simply reflect proliferation/differentiation status and that it appears to be regulated in a more complex way.

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Year:  1998        PMID: 9664900     DOI: 10.1002/(SICI)1096-9896(199804)184:4<351::AID-PATH1235>3.0.CO;2-C

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  36 in total

1.  Structure and expression of the human p68 RNA helicase gene.

Authors:  O G Rössler; P Hloch; N Schütz; T Weitzenegger; H Stahl
Journal:  Nucleic Acids Res       Date:  2000-02-15       Impact factor: 16.971

2.  Rearrangement of structured RNA via branch migration structures catalysed by the highly related DEAD-box proteins p68 and p72.

Authors:  O G Rössler; A Straka; H Stahl
Journal:  Nucleic Acids Res       Date:  2001-05-15       Impact factor: 16.971

3.  The highly related DEAD box RNA helicases p68 and p72 exist as heterodimers in cells.

Authors:  V C Ogilvie; B J Wilson; S M Nicol; N A Morrice; L R Saunders; G N Barber; F V Fuller-Pace
Journal:  Nucleic Acids Res       Date:  2003-03-01       Impact factor: 16.971

4.  Reduced levels of DEAD-box proteins DBP-RB and p72 in fetal Down syndrome brains.

Authors:  Susanne G Kircher; Seong Hwan Kim; Michael Fountoulakis; Gert Lubec
Journal:  Neurochem Res       Date:  2002-10       Impact factor: 3.996

5.  Tobacco VDL gene encodes a plastid DEAD box RNA helicase and is involved in chloroplast differentiation and plant morphogenesis.

Authors:  Y Wang; G Duby; B Purnelle; M Boutry
Journal:  Plant Cell       Date:  2000-11       Impact factor: 11.277

6.  p68 RNA helicase is an essential human splicing factor that acts at the U1 snRNA-5' splice site duplex.

Authors:  Zhi-Ren Liu
Journal:  Mol Cell Biol       Date:  2002-08       Impact factor: 4.272

Review 7.  RNA helicases: emerging roles in viral replication and the host innate response.

Authors:  Arnaz Ranji; Kathleen Boris-Lawrie
Journal:  RNA Biol       Date:  2010-11-01       Impact factor: 4.652

8.  The expression of RNA helicase DDX5 is transcriptionally upregulated by calcitriol through a vitamin D response element in the proximal promoter in SiHa cervical cells.

Authors:  Ramiro José González-Duarte; Verna Cázares-Ordoñez; Lorenza Díaz; Víctor Ortíz; Fernando Larrea; Euclides Avila
Journal:  Mol Cell Biochem       Date:  2015-08-28       Impact factor: 3.396

9.  The DEAD box protein p68: a novel transcriptional coactivator of the p53 tumour suppressor.

Authors:  Gaynor J Bates; Samantha M Nicol; Brian J Wilson; Anne-Marie F Jacobs; Jean-Christophe Bourdon; Julie Wardrop; David J Gregory; David P Lane; Neil D Perkins; Frances V Fuller-Pace
Journal:  EMBO J       Date:  2005-01-20       Impact factor: 11.598

10.  The DEAD-box protein p72 regulates ERalpha-/oestrogen-dependent transcription and cell growth, and is associated with improved survival in ERalpha-positive breast cancer.

Authors:  N C Wortham; E Ahamed; S M Nicol; R S Thomas; M Periyasamy; J Jiang; A M Ochocka; S Shousha; L Huson; S E Bray; R C Coombes; S Ali; F V Fuller-Pace
Journal:  Oncogene       Date:  2009-08-31       Impact factor: 9.867

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