Nucleotide sequence and promoter analysis of SPO13, a meiosis-specific gene of Saccharomyces cerevisiae

The SPO13 gene, required for meiosis I segregation in Saccharomyces cerevisiae, produces two developmentally regulated transcripts (1.0 and 1.4 kilobases) that differ in length at their 5' ends. The shorter transcript is sufficient to complement the spo13-1 mutation and contains a major open re...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 87; no. 23; pp. 9406 - 9410
Main Authors Buckingham, L.E. (University of Chicago, Chicago, IL), Wang, H.T, Elder, R.T, McCarroll, R.M, Slater, M.R, Esposito, R.E
Format Journal Article
LanguageEnglish
Published Washington, DC National Academy of Sciences of the United States of America 01.12.1990
National Acad Sciences
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Summary:The SPO13 gene, required for meiosis I segregation in Saccharomyces cerevisiae, produces two developmentally regulated transcripts (1.0 and 1.4 kilobases) that differ in length at their 5' ends. The shorter transcript is sufficient to complement the spo13-1 mutation and contains a major open reading frame encoding a highly basic protein of 33.4 kilodaltons. A fragment upstream (-170 to -8) of the open reading frame confers meiosis-specific transcription on a spo13-HIS3 fusion. Deletions at the 5' end of spo13-lacZ fusions define a region between -140 and -80 that is essential for meiosis-specific expression. This region acts in an orientation-independent manner and is responsive to the MAT-RME regulatory cascade. It contains a 10-base-pair sequence, TAGCCGCCGA, found in a number of meiosis-specific genes, that appears to be required for SPO13 expression. This sequence is identical to URS1, a ubiquitous mitotic repressor element.
Bibliography:F60
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9120179
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content type line 23
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.87.23.9406