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Home >> Plant Biotechnology and Genomics >>Whole Genome Sequencing and Functional Genomics >> Maize (Zea Mays) Genome

Maize (Zea mays) Genome
The maize genome is almost as big in size as the human genome (~2.5 to 3.0 billion base pairs) and is highly repetitive with 65-80% of the genome consisting of retrotransposons, and another small fraction consisting of MITEs (miniature inverted transposable elements). Therefore, sequencing of this genome will be expensive and difficult. Nevertheless, a maize genome sequencing project is being initiated in USA. Since, maize genome differs from rice genome by as many as 15,000 rearrangements, it was believed that rice will be too distant to facilitate map based cloning in maize and other cereals like wheat, barley, sorghum, and oats.

The genome projects so far utilized either a minimal tiling approach or a whole genome shotgun (WGS) sequencing followed by computer assembly approach, the latter becoming difficult for maize genome due to its highly repetitive nature. None of these two approaches were considered suitable or desirable in case of maize genome. A third option, therefore, was considered desirable, which would involve identification, sequencing and assembly of all maize genes, which number approximately 50,000 and account for as little as 10-15% of the whole genome. Gene rich regions can be identified due to methylation patterns, since only the gene rich regions, and not the repetitive DNA, get methylated; DNA with high Cot values and regions adjoining the transposons will also be enriched in genes.

This strategy would involve sequencing of only the gene-rich regions and not the sequencing of large proportion of the genome involving the repetitive region, thus reducing the work substantially. It was also agreed that the inbred B73 should be utilized for genome sequencing, since it is already being used for developing a BAC physical map and the ESTs.

In the year 2001, data on complete sequence of about 150 maize genes and several BAC clones and the shotgun sequencing of about 5000 random maize genomic clones were already available. More BACs were being sequenced during 2001-02 under various genome projects that were being funded at that time. A physical map involving BAC clones and the corresponding contigs and the anchor markers was estimated to be ready by spring (March-April) of 2003, which was considered essential for the maize genome sequencing project. The complete genome (only the gene rich regions) is estimated to be completed by the year 2005.

 

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