Transcription of mouse Sp2 yields alternatively spliced and sub-genomic mRNAs in a tissue- and cell-type-specific fashion
The Sp-family of transcription factors is comprised by nine members, Sp1-9, that share a highly conserved DNA-binding domain. Sp2 is a poorly characterized member of this transcription factor family that is widely expressed in murine and human cell lines yet exhibits little DNA-binding or trans-acti...
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Published in | Biochimica et biophysica acta Vol. 1799; no. 7; pp. 520 - 531 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.07.2010
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Subjects | |
Online Access | Get full text |
ISSN | 1874-9399 0006-3002 1876-4320 |
DOI | 10.1016/j.bbagrm.2010.03.002 |
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Summary: | The Sp-family of transcription factors is comprised by nine members,
Sp1-9, that share a highly conserved DNA-binding domain.
Sp2 is a poorly characterized member of this transcription factor family that is widely expressed in murine and human cell lines yet exhibits little DNA-binding or
trans-activation activity in these settings. As a prelude to the generation of a “knock-out” mouse strain, we isolated a mouse
Sp2 cDNA and performed a detailed analysis of
Sp2 transcription in embryonic and adult mouse tissues. We report that (1) the 5′ untranslated region of
Sp2 is subject to alternative splicing, (2)
Sp2 transcription is regulated by at least two promoters that differ in their cell-type specificity, (3) one
Sp2 promoter is highly active in nine mammalian cell lines and strains and is regulated by at least five discrete stimulatory and inhibitory elements, (4) a variety of sub-genomic messages are synthesized from the
Sp2 locus in a tissue- and cell-type-specific fashion and these transcripts have the capacity to encode a novel partial-Sp2 protein, and (5) RNA
in situ hybridization assays indicate that
Sp2 is widely expressed during mouse embryogenesis, particularly in the embryonic brain, and robust
Sp2 expression occurs in neurogenic regions of the post-natal and adult brain. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 1874-9399 0006-3002 1876-4320 |
DOI: | 10.1016/j.bbagrm.2010.03.002 |