Bacterial artificial chromosome

Bacterial artificial chromosome

A bacterial artificial chromosome (BAC) is a DNA construct, based on a functional fertility plasmid (or F-plasmid), used for transforming and cloning in bacteria, usually E. coli.[1][2] F-plasmids play a crucial role because they contain partition genes that promote the even distribution of plasmids after bacterial cell division. The bacterial artificial chromosome's usual insert size is 150-350 kbp, but can be greater than 700 kbp.[3] A similar cloning vector called a PAC has also been produced from the bacterial P1-plasmid.

BACs are often used to sequence the genome of organisms in genome projects, for example the Human Genome Project. A short piece of the organism's DNA is amplified as an insert in BACs, and then sequenced. Finally, the sequenced parts are rearranged in silico, resulting in the genomic sequence of the organism.


Common gene components

oriS, repE - F
for plasmid replication and regulation of copy number.
parA and parB
for partitioning F plasmid DNA to daughter cells during division and ensures stable maintenance of the BAC.
A selectable marker
for antibiotic resistance; some BACs also have lacZ at the cloning site for blue/white selection.
T7 & Sp6
phage promoters for transcription of inserted genes.

Contribution to models of disease

Inherited disease

BACs are now being utilized to a greater extent in modelling genetic diseases, often alongside transgenic mice. BACs have been useful in this field as complex genes may have several regulatory sequences upstream of the encoding sequence, including various promoter sequences that will govern a gene's expression level. BACs have been used to some degree of success with mice when studying neurological diseases such as Alzheimer's disease or as in the case of aneuploidy associated with Down syndrome. There have also been instances when they have been used to study specific oncogenes associated with cancers. They are transferred over to these genetic disease models by electroporation/transformation, transfection with a suitable virus or microinjection. BACs can also be utilised to detect genes or large sequences of interest and then used to map them onto the human chromosome using BAC arrays. BACs are preferred for these kind of genetic studies because they accommodate much larger sequences without the risk of rearrangement, and are therefore more stable than other types of cloning vectors.[citation needed]

Infectious disease

The genomes of several large DNA viruses and RNA viruses have been cloned as BACs. These constructs are referred to as "infectious clones", as transfection of the BAC construct into host cells is sufficient to initiate viral infection. The infectious property of these BACs has made the study of many viruses such as the herpesviruses, poxviruses and coronaviruses more accessible.[4][5][6] Molecular studies of these viruses can now be achieved using genetic approaches to mutate the BAC while it resides in bacteria. Such genetic approaches rely on either linear or circular targeting vectors to carry out homologous recombination.[7]

See also


  1. ^ O'Connor M, Peifer M, Bender W (1989). "Construction of large DNA segments in Escherichia coli". Science 244 (4910): 1307–1312. doi:10.1126/science.2660262. PMID 2660262. 
  2. ^ Shizuya H, Birren B, Kim U-J, Mancino V, Slepak T, Tachiiri Y, Simon M (1992). "Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coli using an F-factor-based vector". Proc Natl Acad Sci USA 89 (18): 8794–8797. doi:10.1073/pnas.89.18.8794. PMC 50007. PMID 1528894. 
  3. ^ Stone NE, Fan J-B, Willour V, Pennacchio LA, Warrington JA, Hu A, Chapelle A, Lehesjoki A-E, Cox DR, Myers RM (1996). "Construction of a 750-kb bacterial clone contig and restriction map in the region of human chromosome 21 containing the progressive myoclonus epilepsy gene". Genome Research 6 (3): 218–225. doi:10.1101/gr.6.3.218. PMID 8963899. 
  4. ^ Almazan F, Gonzalez JM, Penzes Z, Izeta A, Calvo E, Plana-Duran J, Enjuanes L (2000). "Engineering the largest RNA virus genome as an infectious bacterial artificial chromosome". Proc Natl Acad Sci USA 97 (10): 5516–5521. doi:10.1073/pnas.97.10.5516. PMC 25860. PMID 10805807. 
  5. ^ Domi A, Moss B (2002). "Cloning the vaccinia virus genome as a bacterial artificial chromosome in Escherichia coli and recovery of infectious virus in mammalian cells". Proc Natl Acad Sci USA 99 (19): 12415–12420. doi:10.1073/pnas.192420599. PMC 129459. PMID 12196634. 
  6. ^ Messerle M, Crnkovic I, Hammerschmidt W, Ziegler H, Koszinowski UH (1997). "Cloning and mutagenesis of a herpesvirus genome as an infectious bacterial artificial chromosome". Proc Natl Acad Sci USA 94 (26): 14759–14763. doi:10.1073/pnas.94.26.14759. PMC 25110. PMID 9405686. 
  7. ^ Feederle, Regina, Emmalene J. Bartlett, and Henri-Jacques Delecluse. "Epstein-Barr Virus Genetics: Talking about the BAC Generation." Herpesviridae. BioMed Central, 7 Dec. 2010. Web. <>.

External links

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  • P1-derived artificial chromosome — The P1 derived artificial chromosome are DNA constructs that are derived from the DNA of P1 bacteriophage. They can carry large amounts (about 100 300 kilobases) of other sequences for a variety of bioengineering purposes. It is one type of… …   Wikipedia

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