MOLECULAR-CLONING AND ANALYSIS OF THE YEAST FLOCCULATION GENE FLO1

被引:126
作者
WATARI, J
TAKATA, Y
OGAWA, M
SAHARA, H
KOSHINO, S
ONNELA, ML
AIRAKSINEN, U
JAATINEN, R
PENTTILA, M
KERANEN, S
机构
[1] VTT, BIOTECH LAB, SF-02151 ESPOO, FINLAND
[2] SAPPORO BREWERIES LTD, BREWING RES LAB, SHIZUOKA 425, JAPAN
关键词
YEAST FLOCCULATION; FLO1; REPEATED SEQUENCES; LECTIN;
D O I
10.1002/yea.320100208
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The DNA sequence of the flocculation gene FLO1 of Saccharomyces cerevisiae, which is located on chromosome I (Watari et al., 1989) was determined. The sequence contains a large open reading frame (ORF) of 2586 bp and codes for a protein of 862 amino acids. However, further study (genomic Southern and polymerase chain reaction analyses) indicated that the gene we cloned was not the intact FLO1 gene but a form with an approximately 2 kb deletion in the ORF region. The intact FLO1 gene was then cloned and its nucleotide sequence determined. The sequence revealed that the ORF of the intact gene is composed of 4611 bp which code for a protein of 1537 amino acids. A remarkable feature of the putative Flo1 protein is that it contains four families of repeated sequences composed of 18, 2, 3 and 3 repeats and that it has a large number of serines and threonines. In the deleted FLO1 form, a large part of these repeated sequences was missing. The N- and C-terminal regions are hydrophobic and both contain a potential membrane-spanning region, suggesting that the Flo1 protein is an integral membrane protein and a cell wall component.
引用
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页码:211 / 225
页数:15
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