Yoshioka Y, Fujita Y, Ohtsubo E
Institute of Applied Microbiology, University of Tokyo, Japan.
J Mol Biol. 1990 Jul 5;214(1):39-53. doi: 10.1016/0022-2836(90)90145-C.
The nucleotide sequence of the promoter-distal region of the tra operon of R100 was determined. There are five open reading frames in the region between traT and finO, and their protein products were identified. Nucleotide sequences of plasmid F corresponding to the junction regions among the open reading frames seen in R100 were also determined. Comparison of these nucleotide sequences revealed strong homology in the regions containing traD, traI and an open reading frame (named orfD). The TraD protein (83,899 Da) contains three hydrophobic regions, of which two are located near the amino-terminal region. This protein also contains a possible ATP-binding consensus sequence at the amino-terminal region and a characteristic repeated peptide sequence (Gln-Gln-Pro)10 at the carboxy-terminal region. The TraI protein (191,679 Da) contains the sequence motif conserved in an ATP-dependent DNA helicase superfamily in its carboxy-terminal region. The protein product of orfD, which is probably a new tra gene (named traX), contains 65% hydrophobic amino acids, especially rich in alanine and leucine. There exist non-homologous regions between R100 and F that could be represented as four I-D (insertion or deletion) loops in heteroduplex molecules. Assignment of each loop to the strand of R100 or F was , however, found to be the reverse from that previously assumed. The three I-D loops that were located between traT and traD, between traD and traI, and between traI and finO had no terminal inverted repeat sequences nor had they any homology with known insertion sequences, while the fourth was IS3, located within the finO gene of F. The sequences in the I-D loops, except IS3, may also code for proteins that are, however, likely to be nonessential for transfer of plasmids.
测定了R100的tra操纵子启动子远端区域的核苷酸序列。在traT和finO之间的区域有5个开放阅读框,并鉴定了它们的蛋白质产物。还测定了质粒F中与R100中所见开放阅读框之间连接区域相对应的核苷酸序列。这些核苷酸序列的比较揭示了在包含traD、traI和一个开放阅读框(命名为orfD)的区域中有很强的同源性。TraD蛋白(83,899道尔顿)含有三个疏水区域,其中两个位于氨基末端区域附近。该蛋白在氨基末端区域还含有一个可能的ATP结合共有序列,在羧基末端区域含有一个特征性的重复肽序列(Gln-Gln-Pro)10。TraI蛋白(191,679道尔顿)在其羧基末端区域含有ATP依赖性DNA解旋酶超家族中保守的序列基序。orfD的蛋白产物可能是一个新的tra基因(命名为traX),含有65%的疏水氨基酸,尤其富含丙氨酸和亮氨酸。R100和F之间存在非同源区域,在异源双链分子中可表现为四个插入或缺失(I-D)环。然而,发现每个环在R100或F链上的归属与先前假设的相反。位于traT和traD之间、traD和traI之间以及traI和finO之间的三个I-D环没有末端反向重复序列,也与已知插入序列没有同源性,而第四个是IS3,位于F的finO基因内。I-D环中的序列(IS3除外)也可能编码蛋白质,然而这些蛋白质可能对质粒转移并非必需。