Nucleic Acids Research, 1995, Vol. 23, No. 22 4583-4590
© 1995
Articles |
HMG box 4 is the principal determinant of species specificity in the RNA polymerase I transcription factor UBF
Biomedical Research Centre, Ninewells Hospital and Medical School, The University of Dundee Dundee DD1 9SY, UK
*To whom correspondence should be addressed
Received September 7, 1995. Accepted October 12, 1995.
Transcription of ribosomal genes requires, in addition to RNA polymerase I, the trans acting factors UBF and Rlb1 in Xenopus or SL1 in humans. RNA polymerase I transcription is remarkably species specific. Between closely related species SL1 Is the sole determinant of this specificity. Between more distantly related species, however, UBF is also a component of this species specificity. Xenopus UBF cannot function in human RNA polymerase I transcription and human UBF cannot function in Xenopus RNA polymerase I transcription. Xenopus and human UBFs are remarkably similar at the amino acid sequence level, both containing multiple HMG box DNA binding motifs. The only major difference between xUBF and hUBF is the lack of a HMG box 4 equivalent in xUBF. Utilizing a series of hybrid UBF molecules we have identified HMG box 4 as the principal determinant of species specificity. Addition of human HMG box 4 to xUBF converts it to a form that functions In human RNA polymerase I transcription. Deletion of HMG box 4 from hUBF converts it to a form that functions in Xenopus RNA polymerase I transcription. Furthermore, mutations within Xenopus UBF demonstrate that UBF requires a precise arrangement and number of HMG boxes to function in RNA polymerase I transcription.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
K. Gonda, J. Wudel, D. Nelson, N. Katoku-Kikyo, P. Reed, H. Tamada, and N. Kikyo Requirement of the Protein B23 for Nucleolar Disassembly Induced by the FRGY2a Family Proteins J. Biol. Chem., March 24, 2006; 281(12): 8153 - 8160. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. C. O'Sullivan, G. J. Sullivan, and B. McStay UBF Binding In Vivo Is Not Restricted to Regulatory Sequences within the Vertebrate Ribosomal DNA Repeat Mol. Cell. Biol., January 15, 2002; 22(2): 657 - 658. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Y. Stefanovsky, G. Pelletier, D. P. Bazett-Jones, C. Crane-Robinson, and T. Moss DNA looping in the RNA polymerase I enhancesome is the result of non-cooperative in-phase bending by two UBF molecules Nucleic Acids Res., August 1, 2001; 29(15): 3241 - 3247. [Abstract] [Full Text] [PDF] |
||||
![]() |
C Mais and U Scheer Molecular architecture of the amplified nucleoli of Xenopus oocytes J. Cell Sci., January 2, 2001; 114(4): 709 - 718. [Abstract] [PDF] |
||||
![]() |
H. M. Alzuherri and R. J. White Regulation of RNA Polymerase I Transcription in Response to F9 Embryonal Carcinoma Stem Cell Differentiation J. Biol. Chem., February 12, 1999; 274(7): 4328 - 4334. [Abstract] [Full Text] [PDF] |
||||
![]() |
P Bell, C Mais, B McStay, and U Scheer Association of the nucleolar transcription factor UBF with the transcriptionally inactive rRNA genes of pronuclei and early Xenopus embryos J. Cell Sci., January 9, 1997; 110(17): 2053 - 2063. [Abstract] [PDF] |
||||



