Transfer gene
Transfer operon, commonly called tra operon, or tra genes, are some of the genes necessary for non-sexual transfer of genetic material in both gram-positive and gram-negative bacteria. The tra locus includes the pilin gene and regulatory genes, which together form pili on the cell surface, polymeric proteins that can attach themselves to the surface of F- bacteria and initiate the conjugation. The existence of the tra region of a plasmid genome was first discovered in 1979 by David H. Figurski and Donald R. Helinski[1] In the course of their work, Figurski and Helinski also discovered a second key fact about the tra region – that it can act in trans to the mobilization marker which it affects.[1]
This finding suggested that there were two basic aspects necessary for a plasmid to move from one cell to another:
- An origin of transfer – The oriT (or mob) site must be located on the plasmid itself to allow recognition of the plasmid and initiation of transfer.[2] A plasmid with no origin of transfer is non-mobilizable.
- The transfer genes – Though a functioning set of tra genes is necessary for plasmid transfer, they may be located in a variety of places including the plasmid in question, another plasmid in the same host cell, or even in the bacterial genome.[3]
The tra genes encode proteins which are useful for the propagation of the plasmid from the host cell to a compatible donor cell or maintenance of the plasmid. Not all transfer operons are the same. Some genes are only found in a few species or a single genus of bacteria while others (such as traL) are found in very similar forms in many bacterial species. Many of the transfer systems are incompatible. For example, oriT and mob are two origins of transfer which interact with different sets of transfer genes. A plasmid with a mob site (like many found in Rhodococcus species) cannot be transferred via transfer genes which normally interact with the oriT site (which is common in E. coli)[3]
| The roles of some tra-gene encoded proteins:[4] | |
| Pili Assembly and Production | traA, traB, traE, traC, traF, traG, traH, traK, traL, traQ, traU, traV, traW, |
| Inner Membrane Proteins | traB, traE, traG, traL, traP |
| Periplasmic Proteins | traC, traF, traH traK, traU, traW |
| DNA transfer | traC, traD, traI, traM, traY |
| Surface Exclusion Proteins | traS, traT |
| Mating Pair Stabilization | traN, traG |
Each of the individual genes in the tra operon codes for a different protein product. These products may perform a number of tasks including interaction with one another to perform mating pair functions and regulation of different regions of the tra operon itself,[5] or conjugative DNA metabolism and surface exclusion.[4] Also note that some proteins perform multiple functions or are associated closely with proteins which have non-similar functions.
References
- ↑ 1.0 1.1 Figurski D, Helinski D (1979). "Replication of an origin-containing derivative of plasmid RK2 dependent on a plasmid function in trans". PNAS 76 (4): 1648–1652. doi:10.1073/pnas.76.4.1648. PMC 383447. PMID 377280.
- ↑ Fu Y H, Tsai M M, Luo Y N, Deonier R C (1 February 1991). "Deletion analysis of the F plasmid oriT locus.". Journal of Bacteriology 173 (3): 1012–1020. PMC 207219. PMID 1991706.
- ↑ 3.0 3.1 Simon R, Priefer U, Puhler A (1983). "A Broad Host Range Mobilization System for In Vivo Genetic Engineering: Transposon Mutagenesis in Gram Negative Bacteria". Nature Biotechnology 1 (9): 784–791. doi:10.1038/nbt1183-784.
- ↑ 4.0 4.1 Clewell D, et al. (1993). Bacterial Conjugation. Plenum Press, New York. ISBN 0-306-44376-7.
- ↑ Grohmann E, Muth G, Espinosa M (2003). "Conjugative Plasmid Transfer in Gram-Positive Bacteria". Microbiology and Molecular Biology Reviews 67 (2): 277–301. doi:10.1128/MMBR.67.2.277-301.2003. PMC 156469. PMID 12794193.