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J Biol Chem, Vol. 274, Issue 15, 10293-10300, April 9, 1999
Regulation of DNA Binding Activity and Nuclear Transport of
B-Myb in Xenopus Oocytes
Graciela
Humbert-Lan and
Tomas
Pieler
From the Institut für Biochemie und Molekulare Zellbiologie
der Universität Göttingen, Humboldtallee 23, 37073 Göttingen, Germany
DNA binding activity and nuclear transport of
B-Myb in Xenopus oocytes are negatively regulated. Two
distinct sequence elements in the C-terminal portion of the protein are
responsible for these different inhibitory activities. A C-terminal
Xenopus B-Myb protein fragment inhibits the DNA binding
activity of the N-terminal repeats in trans, indicating
that intramolecular folding may result in masking of the DNA binding
function. Xenopus B-Myb contains two separate nuclear
localization signals (NLSs), which, in Xenopus oocytes,
function only outside the context of the full-length protein. Fusion of
an additional NLS to the full-length protein overcomes the inhibition
of nuclear import, suggesting that masking of the NLS function rather
than cytoplasmic anchoring is responsible for the negative regulation
of Xenopus B-Myb nuclear transfer. During
Xenopus embryogenesis, when inhibition of nuclear import is
relieved, Xenopus B-myb is preferentially
expressed in the developing nervous system and neural crest cells.
Within the developing neural tube, Xenopus B-myb
gene transcription occurs preferentially in proliferating,
non-differentiated cells.
Copyright © 1999 by The American Society for Biochemistry and Molecular Biology, Inc.

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Copyright © 1999 by the American Society for Biochemistry and Molecular Biology.
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