A database of PCR primers for the chloroplast genomes of higher plants
© Heinze; licensee BioMed Central Ltd. 2007
Received: 03 November 2006
Accepted: 27 February 2007
Published: 27 February 2007
Chloroplast genomes evolve slowly and many primers for PCR amplification and analysis of chloroplast sequences can be used across a wide array of genera. In some cases 'universal' primers have been designed for the purpose of working across species boundaries. However, the essential information on these primer sequences is scattered throughout the literature.
A database is presented here which assembles published primer information for chloroplast DNA. Additional primers were designed to fill gaps where little or no primer information could be found. Amplicons are either the genes themselves (typically useful in studies of sequence variation in higher-order phylogeny) or they are spacers, introns, and intergenic regions (for studies of phylogeographic patterns within and among species). The current list of 'generic' primers consists of more than 700 sequences. Wherever possible, we give the locations of the primers in the thirteen fully sequenced chloroplast genomes (Nicotiana tabacum, Atropa belladonna, Spinacia oleracea, Arabidopsis thaliana, Populus trichocarpa, Oryza sativa, Pinus thunbergii, Marchantia polymorpha, Zea mays, Oenothera elata, Acorus calamus, Eucalyptus globulus, Medicago trunculata).
The database described here is designed to serve as a resource for researchers who are venturing into the study of poorly described chloroplast genomes, whether for large- or small-scale DNA sequencing projects, to study molecular variation or to investigate chloroplast evolution.
In 1991, Pierre Taberlet published what was probably the first article recommending 'universal' polymerase chain reaction (PCR) primers for use across plant genera and species, with a view to analysing intra-specific variation . The approach has been favourably adopted by the scientific community: a recent search identified 855 citing papers for the original publication (Scholar Google, 25 October 2006; up from 678 in January 2006). New sets of primers have subsequently been published that reflect Taberlet's original intention to study molecular variation among closely related species, or among separate sets of populations within species, by analysing introns and spacers [e.g., [2–5]]. This can be done since chloroplast genes evolve slowly, and primers can be designed with the purpose of working across species. In chloroplast genomes, gene order is highly conserved [2, 3, 5], whereas some spacers show even intra-species variation. Amplified fragments can be analysed by restriction analysis or DNA sequencing. The author's experience is that small insertions/deletions (indels) are relatively frequent, when compared to point mutations that result in restriction site changes [6–8]. Exon sequences are generally highly conserved, but this depends on the gene in question. Molecular systematicists, starting with the highly conserved rbcL gene, and later expanding to e.g. matK, ndhF, rpl16, and atpB, have utilized PCR-amplified chloroplast gene sequences for establishing and verifying phylogenies. Sets of primers recommended for this purpose have also expanded in size [e.g., [9–12]]. We have published a core set of 38 primer pairs useful in the amplification of the large single copy region in angiosperms, but also for fragments of this region in other plants .
As more and more partial and complete chloroplast DNA genome sequences become available, it is apparent that a balanced view on chloroplast sequence variation depends on the choice of many different sites along the genome [10, 11]. It is interesting to notice that different groups of authors tend to work with alternative sets of primers. A central site for primer information should therefore help in making resources that are already there more widely known, and to encourage comparative studies across many laboratories.
Construction and content
Published primer sequences
The primers were initially ordered along the tobacco (Nicotiana tabaccum) chloroplast genome (GenBank:Z00044 and S54304), as this is the best characterised chloroplast genome to date. Orientation of the primers (F, forward; R, reverse) is given relative to the tobacco sequence. These manipulations were mainly done with the Omiga 1.1.3 software (Accelrys, Oxford, UK).
Filling the gaps
Together with Delphine Grivet and Remy Petit (then at INRA-Pierroton, France), primers were designed in order to close any remaining gaps along the large single copy region. As a result of this collaboration, a set of 38 primer pairs spanning this region of the chloroplast genome in angiosperms was published . The primer pairs described in this publication  amplify fragments of between 2000 and 5000 bp in most angiosperm species. Methods for identifying conserved primer binding sites included comparing and aligning chloroplast DNA sequences available in GenBank by eye, with the help of Omiga, by using BLAST , or by using a suite of DOS programs written by John Antoniw [20, 21]. Further primers were developed for this database following the same strategy, in order to fill remaining gaps, to decrease the size of amplicons, or to replace primers with poor performance in our lab. Sufficiently conserved potential primer sites in alignments were visually checked for abnormalities like biased GC/AT percentages, mononucleotide stretches, or apparent palindromes; sites with such features were avoided whenever possible. In some cases, alternative primer sites were designated in close proximity, so that the users can select the ones best matching their taxa of interest.
Positioning primers in sequenced chloroplast genomes
BLASTALL (obtained from NCBI, USA ), was used to search for homologies of the primers in 13 chloroplasts (from GenBank, December 2005, except Populus): Nicotiana tabacum (GenBank:NC_001879.1), Atropa belladonna (GenBank:NC_004561), Spinacia oleracea (GenBank:NC_002202.1), Arabidopsis thaliana (GenBank:NC_000932), Populus trichocarpa [Heinze et al. in preparation, and ], Oryza sativa NC_001320.1, Pinus thunbergii (GenBank:NC_001631.1), Marchantia polymorpha (GenBank:NC_001319.1), Zea mays (GenBank:X86563), Oenothera elata (GenBank:AJ2710796.2), Acorus calamus (GenBank:NC_007407.1), Eucalyptus globulus (GenBank:AY780259.1), and Medicago trunculata (GenBank:NC_003119.6) with an E value cut-off of 0.5. The position of the 5' nucleotide for each primer in the 13 full genome sequences is given whenever sufficient homology (E value below 0.5) was found. For primers with multiple binding sites (e.g., those in the inverted repeats), only the position of the first site is given. There are cases where BLAST returned spurious primer binding sites in some of the species (not in the expected position) and these indicate possible sources for PCR artefacts. Therefore, such primer positions are also included in the database. Different weights were not given to matches in the 5' or 3' ends of the primers in the BLAST search, because in a low-complexity template as the plant chloroplast, even sub-optimal priming may lead to amplification (and consequently, artefacts).
Statistics of database version 2.1
number of database entries*
total number of entries
anchored in Nicotiana tabacum
anchored in Atropa belladonna
anchored in Spinacia oleracea
anchored in Arabidopsis thaliana
anchored in Populus trichocarpa
anchored in Eucalyptus globulus
anchored in Medicago trunculata
anchored in Oenothera elata
anchored in Zea mays
anchored in Oryza sativa
anchored in Acorus
anchored in Pinus thunbergii
anchored in Marchantia polymorpha
present in all 13 chloroplast genomes
present in Nicotiana and Atropa
present in Nicotiana, Atropa and Spinacia
present in Arabidopsis, Populus and Eucalyptus
present in all dicots
present in monocots
present in all 13 but Pinus and Marchantia
present in all 13 but Marchantia
within trn genes
within photosystem genes (psa, psb)
within ribosomal proteins and RNA polymerase (rpl, rps, rpo)
within ATPase genes (atp)
within ycf genes
within NADH-specific dehydrogenase (ndh) genes
Utility and Discussion
Transferring PCR primers to new species has accelerated molecular research tremendously. However, it should be noted that from the early days of chloroplast genome research, when probes and blotting techniques were still in use, cross-species transfer of such gene probes was always possible [e.g., ]. Nevertheless, venturing into unknown species with primers is still a 'trial and error' experience. It is hoped that the availability of a database that includes alternative, tested primers for a number of species will reduce the efforts in such cases. The database can now easily be searched or filtered: a text field is included which allows for free-text searching in any of the fields. For example, this text may be a part of a gene or primer name, an author name in the references (column 'Ref_Src'), or even a part of a primer nucleotide sequence. Additionally, the data can be sorted for the values in any of the fields. Numerical values (e.g., primer length or position in any of the 13 genomes) will be sorted arithmetically, and text values alphabetically. For instance, a search and filter operation for all primers associated with transfer RNA (trn) genes would require typing 'trn' into the filter; the results can be sorted e.g. by species (by entering the column number 11 for e.g. Acorus) or by gene names (column 3). Positioning the mouse over the column headings will show the full name of the columns.
Furthermore, it is possible to combine primers from different publications into newly assembled pairs. 'Generic' PCR conditions that favour successful amplification with such new combinations are standard PCR conditions with the use of 2 mM Mg2+ and a PCR program with 10 cycles at 70°C annealing, followed by 32 cycles at 55°C or 50°C annealing . With these primers and methods, the chloroplast genomes of hitherto unexplored species can be scanned in detail, and regions specific for different purposes picked [e.g. [7, 8]].
The author's recommendation for analysing uncharacterized chloroplast genomes is the following: (i) select a genome from the 13 listed which is phylogenetically close to the species of interest; (ii) sort the database for primer position in the selected genome (leaving the 'filter' field empty so that all primers will be displayed); (iii) select primer pairs in a suitable distance in the selected genome. In this last step, care must be taken to select primer pairs in the correct orientation. This can be done by comparing the gene order in the region of interest with the one in tobacco. In case of similar orientation of the genes, the 'F' and 'R' designations of the primers can be used as given in the database. In case of reverse orientation of the local gene order (relative to tobacco) in the species of interest, primer orientation is also reverse.
Recently, Dhingra and Folta  have suggested using overlapping PCR fragments for sequencing entire chloroplast genomes from total plant DNA preparations. While this approach holds some promise, it must be mentioned that a number of phenomena can interfere with it. Chloroplast DNA fragments are constantly transferred to the nucleus and to the mitochondrion , and extra-chloroplast DNA can lead to artefacts like apparent sequence polymorphisms. We have encountered such polymorphisms in shotgun sequencing of the black poplar (Populus trichocarpa) genomes [Heinze et al. in preparation; ]. The quality of the DNA preparation (relative amounts of nuclear, mitochondrial, and chloroplast DNA) is key to the success of the PCR sequencing strategy. Prior purification of chloroplasts, which has always been a speed-limiting step, will determine the success to a large degree. The advantage of using primers from this database, as opposed to a fixed set of primer pairs, is that it is easy to switch from unsuccessful primers to alternatives, as very often, alternative primer positions close to each other, and degenerate sequences, have been proposed by different authors. It is also easier to generate overlapping sequence when primers are employed in varying combinations.
This version of the database offers the following improvements compared to earlier ones : the database can now be searched, filtered, and sorted online; there are now more than 700 primers (up from 500+); and primer positions are now given in 13 genomes (previously only five). In comparison to the single article introducing the highest number of primers , this database contains almost 10 times as many primers.
We have analysed collections of wild cherry (Prunus avium) and common ash (Fraxinus excelsior) DNAs for variation in chloroplast sequence, using either the PCR-RFLP  or a denaturing high-performance liquid chromatography approach [Heinze in preparation; [8, 26]]. In both cases, it was possible to quickly screen the major part of the large single copy region for variation between samples collected from different sites across the species ranges. In our laboratory, agarose PCR-RFLP is still a first screening method with acceptable throughput, when large sample numbers are analysed. After PCR, samples are scanned on agarose gels for successful amplification. An aliquot of the PCR is treated with restriction enzymes. Restriction polymorphisms and major indels can be detected in high-percentage agarose gels.
Some problems with universal PCR include the more rapid sequence evolution in some parts of the chloroplast; the identification of polymorphisms between conserved primer sites (introns), and occasional rearrangements, deletions, duplications in some genera, families, or higher taxonomic groups. However, rearrangements often only affect one spacer, leaving large blocks of genes with their order conserved. It is often at the breakpoints between conserved blocks of gene order where more sequence variation at lower taxonomic levels can be found.
It is tempting to speculate about poorly characterised chloroplast DNA regions that nevertheless yield conserved primer binding sites. This happens in some introns, but also in a number of spacers, open reading frames (ORFs) or hypothetical conserved reading frames (ycfs).
Conserved 'universal' primers and markers are possible for chloroplast DNA. Polymorphisms can be identified with tested primer sequences from the database. 'Generic' PCR conditions make possible the use of many primers in new combinations. Several opportunities exist for efficient detection and analysis of polymorphisms. It is hoped that this database will prove useful for many diverse problems and that our knowledge of mutation and evolution processes in chloroplasts will subsquently be enhanced, making it possible in the future to postulate informed predictions for poorly characterized species. Additions to the database (by e-mail to the author) are welcome.
Availability and requirements
Bill Hahn, Delphine Grivet, Remy Petit, Kevin Livingstone and Kurt Weising are gratefully acknowledged for their communications. For additional laboratory work, the author thanks Elmar Kickingereder, Nigel Austin, Irena Nanista, and Aydin Türkeç. Hans Hauer has implemented the search/filter/sort version of the online database. Two anonymous reviewers have provided helpful comments.
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