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Journal of Biological Chemistry
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Fundamental Cellular Processes Do Not Require Vertebrate-specific Sequences within the TATA-binding Protein

Authors: Schmidt, Edward E; Bondareva, Alla A; Radke, Jay R; Capecchi, Mario R;

Fundamental Cellular Processes Do Not Require Vertebrate-specific Sequences within the TATA-binding Protein

Abstract

The 180-amino acid core of the TATA-binding protein (TBPcore) is conserved from Archae bacteria to man. Vertebrate TBPs contain, in addition, a large and highly conserved N-terminal region that is not found in other phyla. We have generated a line of mice in which the tbp allele is replaced with a version, tbp(Delta N), which lacks 111 of 135 N-terminal amino acid residues. Most tbp(Delta N/Delta N) fetuses die in midgestation. To test whether a disruption of general cellular processes contributed to this fetal loss, primary fibroblast cultures were established from +/+, Delta N/+, and Delta N/Delta N fetuses. The cultures exhibited no genotype-dependent differences in proliferation or in expression of the proliferative markers dihydrofolate reductase (DHFR) mRNA (S phase-specific) and cdc25B mRNA (G(2)-specific). The mutation had no effect on transcription initiation site fidelity by either RNA polymerase II (pol II) or pol III. Moreover, the mutation did not cause differences in levels of U6 RNA, a pol III-dependent component of the splicing machinery, in mRNA splicing efficiency, in expression of housekeeping genes from either TATA-containing or TATA-less promoters, or in global gene expression. Our results indicated that general eukaryotic cell functions are unaffected by deletion of these vertebrate-specific sequences from TBP. Thus, all activities of this polypeptide domain must either be compensated for by redundant activities or be restricted to situations that are not represented by primary fibroblasts.

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Keywords

570, Fibroblasts - physiology, Embryo, Nonmammalian, Transcription, Genetic, Cells, Knockout, Fibroblasts - cytology, 610, Messenger - genetics, TATA-Box Binding Protein - chemistry, Mice, Genetic, Species Specificity, Animals, RNA, Messenger, Cells, Cultured, DNA Primers, Sequence Deletion, Mice, Knockout, Cultured, Nonmammalian, Reverse Transcriptase Polymerase Chain Reaction, Mammalian, Fibroblasts, Embryo, Mammalian, TATA-Box Binding Protein, Gene Expression Regulation, Embryo, Gene Expression Regulation - physiology, TATA-Box Binding Protein - genetics, Protein Biosynthesis, Vertebrates, RNA, Transcription, TATA-Box Binding Protein - metabolism

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
18
Average
Average
Top 10%
gold