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Resistance to S. turcica has mainly been characterized in maize.
So far, only seven ZmCPKs (ZmCK1, ZmCDPK1, ZmCDPK2, ZmCDPK7, ZmCDPK9, ZmCDPK10 and ZmCDPK11) have been characterized in maize.
Recently, a new semidominant liguleless mutant, Liguleless narrow (Lgn-R), has been characterized in maize that affects ligule and auricle development and results in a narrow leaf phenotype.
Although some Hsf genes have been characterized in maize, analysis of the entire Hsf gene family were not completed following Maize (B73) Genome Sequencing Project.
Although three NAS genes have been characterized in maize, there is still no systematic identification of maize NAS family by genomic mining.
Many families of transposons have been characterized in maize, and two of these, the Ac/ Ds system and Robertson's Mutator, have been harnessed to create sequence-indexed transposon insertion databases for mutant screening (Settles et al. 2007; Vollbrecht et al. 2010).
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Cell expansion in response to drought has been characterized in the maize (Zea mays) root system as an adaptation to low water potential [ 53].
In comparison with Arabidopsis and rice, less development-regulated genes and their functions in maize have been characterized in detail.
To date, numerous lesion mimic mutants (LMM) have been characterized in Arabidopsis thaliana, rice and maize [ 1, 2].
SNPs have been characterized in crop plant genomes such as maize, sugarbeet, barley, soybean, wheat, rice and grapevine [ 29].
The first draft of full maize genome assembly has recently been released, however, to our knowledge, the ARF gene family from maize (ZmARF genes) has not been characterized in detail.
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