Photosynthetic Mutant Library (PML)

A genetic resource in maize that is tailored for studies of chloroplast biogenesis

PML is a library of Mu- induced non-photosynthetic maize mutants, corresponding DNA samples, and phenotypic data. Mutants contributed to PML exhibit either a seedling chlorophyll deficiency (e.g. pale green, yellow, virescent, albino, or striated leaves) or a high chlorophyll fluorescent (hcf) phenotype. Prior studies indicate that a disruption of most any step in the biogenesis of the chloroplast (i.e. chloroplast gene expression, lipid or pigment synthesis, light perception, membrane assembly, protein import) results in one of the phenotypes contributed to PML. The collection consists of ~2200 independently-arising mutants. We believe that it is near saturation for the screen that was used to assemble the collection, because multiple mutant alleles are invariably recovered for genes for which at least one mutant allele with a non-photosynthetic phenotype is recovered.

Researchers can use this resource in two distinct ways. The pooled DNA samples can be used as a "reverse genetic resource" to identify mutants with Mu insertions in genes of known sequence with a postulated role in chloroplast biogenesis. Alternatively, the phenotype database (a catalog of pigment deficiency, photosynthetic enzyme content and chloroplast RNA defects) can be searched for phenotypes of interest, and corresponding seed requested.

PML as a source of mutant alleles of genes of known sequence

The PML collection is anticipated to include mutations in the vast majority of genes that play non-redundant roles in the establishment of a photosynthetically-competent chloroplast. The relatively small number of DNA samples can be screened by PCR in a cost-effective manner for Mu insertions into genes of known sequence with proposed roles in chloroplast biogenesis. It can be used to obtain the first mutant alleles in genes of known sequence, or to provide additional alleles of genes for which one mutant allele is already available.

Which reverse genetic resource is best for my project?

Several resources related to PML are now available to all academic researchers: maize MTM Mutator lines, Arabidopsis T-DNA populations and transposon lines in Arabidopsis and maize for which sequence tags flanking transposon-insertions are being generated. Each has different attributes which suits it for distinct purposes.

Choice #1: Maize vs Arabidopsis

Factors to consider:

The large maize seed supports the robust growth of non-photosynthetic seedlings (see image of 10 day old albino seedling (~0.5gm leaf tissue) growing happily in soil ), facilitating biochemical analyses of mutant leaf tissue. Although non-photosynthetic Arabidopsis mutants can be grown on sterile sugar medium, this is costly and slow, and alters the physiology of the plant in ways that may confound the interpretation of mutant phenotypes.

Arabidopsis is much more easily transformed. Arabidopsis mutants are best suited for approaches that require the frequent generation of transgenic plants.

Mutations that cause severe and global defects in chloroplast gene expression (e.g. the complete loss of plastid ribosomes) can be recovered in maize but may not be recoverable in Arabidopsis due to the presence of genes in the Arabidopsis chloroplast genome that are required for cell viability.

The availability of the entire Arabidopsis genome sequence offers opportunities that are not yet available in maize. However, it is often possible to predict orthologous relationships between Arabidopsis genes and maize EST sequences, simplifying movement between the two organisms.

Bottom line: a combined approach will often be the best!

Choice #2: MTM vs PML vs RescueMu.

Advantages of MTM and RescueMu sequence tags: no presupposition about mutant phenotype, therefore hits may be recovered in genes whose disruption results in no obvious mutant phenotype or in an embryo lethal phenotype. Such mutants will not be recovered in PML.

RescueMu sequence tag screening has the advantage that screens are done in silico. However, the number of such sequence tags is currently rather limited.

For both these resources, as for PML, users need to establish whether hits detected represent germinal or somatic insertions, and whether they are genetically-linked to any mutant phenotype detected..

If a mutation in your gene does result in one of the phenotypes in the PML collection, it will be advantageous to screen PML. Less time will be spent sorting through useless alleles in which the Mu insertion does not disrupt gene function.

Bottom line: If you are confident that your protein is chloroplast-localized and have good reason to believe that it plays a role in chloroplast gene expression or the assembly or functioning of the photosynthetic apparatus, PML is probably the best place to start. It doesn't cost much and may get you useful mutants more easily than MTM. If PML comes up empty, try MTM!

 

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