Characterization of sams genes of Amoeba proteus and the endosymbiotic X-bacteria

被引:12
作者
Jeon, TJ [1 ]
Jeon, KW [1 ]
机构
[1] Univ Tennessee, Dept Biochem, Knoxville, TN 37996 USA
关键词
amoeba; endosymbionts; nucleotide sequence; S-adenosylmethionine synthetase; SAM; symbiosis;
D O I
10.1111/j.1550-7408.2003.tb00107.x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
As a result of harboring obligatory bacterial endosymbionts, the xD strain of Amoeba proteus no longer produces its own S-adenosylmethionine synthetase (SAMS). When symbiont-free D amoebae are infected with symbionts (X-bacteria), the amount of amoeba SAMS decreases to a negligible level within four weeks, but about 47% of the SAMS activity, which apparently comes from another source, is still detected. Complete nucleotide sequences of sams genes of D and xD amoebae are presented and show that there are no differences between the two. Long-established xD amoebae contain an intact sams gene and thus the loss of xD amoeba's SAMS is not due to the loss of the gene itself. The open reading frame of the amoeba's sams gene has 1,281 nucleotides, encoding SAMS of 426 amino acids with a mass of 48 kDa and pI of 6.5. The amino acid sequence of amoeba SAMS is longer than the SAMS of other organisms by having an extra internal stretch of 28 amino acids. The 5'-flanking region of amoeba sams contains consensus-binding sites for several transcription factors that are related to the regulation of sams genes in E. coli and yeast. The complete nucleotide sequence of the symbiont's sams gene is also presented. The open reading frame of X-bacteria sams is 1, 146 nucleotides long, encoding SAMS of 381 amino acids with a mass of 41 kDa and pI of 6.0. The X-bacteria SAMS has 45% sequence identity with that of A. Proteus.
引用
收藏
页码:61 / 69
页数:9
相关论文
共 29 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]  
Ausubel F.M., 1992, CURRENT PROTOCOLS MO
[3]   Met31p and Met32p, two related zinc finger proteins, are involved in transcriptional regulation of yeast sulfur amino acid metabolism [J].
Blaiseau, PL ;
Isnard, AD ;
SurdinKerjan, Y ;
Thomas, D .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (07) :3640-3648
[4]   WEIGHT MATRIX DESCRIPTIONS OF 4 EUKARYOTIC RNA POLYMERASE-II PROMOTER ELEMENTS DERIVED FROM 502 UNRELATED PROMOTER SEQUENCES [J].
BUCHER, P .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 212 (04) :563-578
[5]   Inhibition of liver methionine adenosyltransferase gene expression by 3-methylcolanthrene:: protective effect of S-adenosylmethionine [J].
Carretero, MV ;
Latasa, MU ;
Garcia-Trevijano, ER ;
Corrales, FJ ;
Wagner, C ;
Mato, JM ;
Avila, MA .
BIOCHEMICAL PHARMACOLOGY, 2001, 61 (09) :1119-1128
[6]   Evidence for symbiont-induced alteration of a host's gene expression: Irreversible loss of SAM synthetase from Amoeba proteus [J].
Choi, JY ;
Lee, TW ;
Jeon, KW ;
Ahn, TI .
JOURNAL OF EUKARYOTIC MICROBIOLOGY, 1997, 44 (05) :412-419
[7]  
Goldstein L, 1976, Methods Cell Biol, V13, P239, DOI 10.1016/S0091-679X(08)61805-1
[8]   In vitro evolution of the DNA binding sites of Escherichia coli methionine repressor, MetJ [J].
He, YY ;
Stockley, PG ;
Gold, L .
JOURNAL OF MOLECULAR BIOLOGY, 1996, 255 (01) :55-66
[9]   Expanding the TRANSFAC database towards an expert system of regulatory molecular mechanisms [J].
Heinemeyer, T ;
Chen, X ;
Karas, H ;
Kel, AE ;
Kel, OV ;
Liebich, I ;
Meinhardt, T ;
Reuter, I ;
Schacherer, F ;
Wingender, E .
NUCLEIC ACIDS RESEARCH, 1999, 27 (01) :318-322
[10]  
Hilti N, 2000, YEAST, V16, P1