Genetic Analysis of the Surface Protein Antigen Gene Expression in Streptococcus mutans

Author(s):  
Toshihiko Koga ◽  
Yoshihisa Yamashita ◽  
Yuichi Tsukioka ◽  
Yoshio Nakano ◽  
Yukie Shibata
1989 ◽  
Vol 3 (2) ◽  
pp. 221-228 ◽  
Author(s):  
N. Okahashi ◽  
C. Sasakawa ◽  
M. Yoshikawa ◽  
S. Hamada ◽  
T. Koga

1990 ◽  
Vol 58 (9) ◽  
pp. 2929-2934 ◽  
Author(s):  
M Iwaki ◽  
N Okahashi ◽  
I Takahashi ◽  
T Kanamoto ◽  
Y Sugita-Konishi ◽  
...  

1993 ◽  
Vol 61 (10) ◽  
pp. 4344-4349 ◽  
Author(s):  
M Nakai ◽  
N Okahashi ◽  
H Ohta ◽  
T Koga

Genetics ◽  
1992 ◽  
Vol 130 (1) ◽  
pp. 97-104
Author(s):  
D L Smith ◽  
F P Doerder

Abstract Genes at the SerH locus of the ciliated protist Tetrahymena thermophila specify the major (H) surface protein on cells grown at 20-36 degrees. Alternative proteins L, T, S and I are expressed under different conditions of temperature and culture media. Mutants unable to express SerH genes were examined for expression of these proteins, also called immobilization or i-antigens, at both H and non-H conditions. In all instances, one or more i-antigens were expressed in the absence of H, and, in most instances, expression of i-antigens under non-H conditions was also affected. Examples of the latter include both the continued expression of H-replacement antigens and the inability to express certain other i-antigens. Such multiple effects were observed in mutants with trans-acting (rseA, rseB, rseC, RseD) and cis-acting (H1-1 and H1-2) mutations, but not in mutants in which SerH is affected developmentally (B2092, B2101, B2103, B2107). These interactions suggest that the wild-type genes identified by mutation exert both positive and negative effects in the regulation of i-antigen gene expression.


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