NDLI: Exonuclease I of Saccharomyces cerevisiae functions in mitotic recombination in vivo and in vitro.

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Hormonal regulation of an islet-specific enhancer in the pancreatic homeobox gene STF-1.

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GRIP1, a transcriptional coactivator for the AF-2 transactivation domain of steroid, thyroid, retinoid, and vitamin D receptors.

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Exonuclease I of Saccharomyces cerevisiae functions in mitotic recombination in vivo and in vitro.

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Frameshift intermediates in homopolymer runs are removed efficiently by yeast mismatch repair proteins.

Microsatellite instability in yeast: dependence on repeat unit size and DNA mismatch repair genes.

Hypermutability of homonucleotide runs in mismatch repair and DNA polymerase proofreading yeast mutants.

The repeat organizer, a specialized insulator element within the intergenic spacer of the Xenopus rRNA genes.

DNA binding by MADS-box transcription factors: a molecular mechanism for differential DNA bending.

A yeast TATA-binding protein mutant that selectively enhances gene expression from weak RNA polymerase II promoters.

Analysis of the receptor binding domain of Gpa1p, the G(alpha) subunit involved in the yeast pheromone response pathway.

Evolutionary conservation of regulatory strategies for the sex determination factor transformer-2.

Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism.

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A minimal spliceosomal complex A recognizes the branch site and polypyrimidine tract.

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Conserved intron elements repress splicing of a neuron-specific c-src exon in vitro.

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Exonuclease I of Saccharomyces cerevisiae functions in mitotic recombination in vivo and in vitro.

Content Provider	PubMed Central
Author	Fiorentini, P. Huang, K. N. Kolodner, R. D. Symington, L. S. Tishkoff, D. X.
Abstract	We previously described a 5'-3' exonuclease required for recombination in vitro between linear DNA molecules with overlapping homologous ends. This exonuclease, referred to as exonuclease I (Exo I), has been purified more than 300-fold from vegetatively grown cells and copurifies with a 42-kDa polypeptide. The activity is nonprocessive and acts preferentially on double-stranded DNA. The biochemical properties are quite similar to those of Schizosaccharomyces pombe Exo I. Extracts prepared from cells containing a mutation of the Saccharomyces cerevisiae EXO1 gene, a homolog of S. pombe exo1, had decreased in vitro recombination activity and when fractionated were found to lack the peak of activity corresponding to the 5'-3' exonuclease. The role of EXO1 on recombination in vivo was determined by measuring the rate of recombination in an exo1 strain containing a direct duplication of mutant ade2 genes and was reduced sixfold. These results indicate that EXO1 is required for recombination in vivo and in vitro in addition to its previously identified role in mismatch repair.
Starting Page	2764
File Format	PDF
ISSN	10985549
e-ISSN	10985549
Journal	Molecular and Cellular Biology
Issue Number	5
Volume Number	17
Language	English
Publisher Date	1997-05-01
Access Restriction	Open
Subject Keyword	Research in Higher Education
Content Type	Text
Resource Type	Article
Subject	Cell Biology Molecular Biology

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