Literature DB >> 15085449

Sequence analysis of the long arm of rice chromosome 11 for rice-wheat synteny.

Nagendra K Singh1, Saurabh Raghuvanshi, Subodh K Srivastava, Anupama Gaur, Ajit K Pal, Vivek Dalal, Archana Singh, Irfan A Ghazi, Ashutosh Bhargav, Mahavir Yadav, Anupam Dixit, Kamlesh Batra, Kishor Gaikwad, Tilak R Sharma, Amitabh Mohanty, Arvind K Bharti, Anita Kapur, Vikrant Gupta, Dibyendu Kumar, Shubha Vij, Ravi Vydianathan, Parul Khurana, Sulabha Sharma, W Richard McCombie, Joachim Messing, Rod Wing, Takuji Sasaki, Paramjit Khurana, Trilochan Mohapatra, Jitendra P Khurana, Akhilesh K Tyagi.   

Abstract

The DNA sequence of 106 BAC/PAC clones in the minimum tiling path (MTP) of the long arm of rice chromosome 11, between map positions 57.3 and 116.2 cM, has been assembled to phase 2 or PLN level. This region has been sequenced to 10x redundancy by the Indian Initiative for Rice Genome Sequencing (IIRGS) and is now publicly available in GenBank. The region, excluding overlaps, has been predicted to contain 2,932 genes using different software. A gene-by-gene BLASTN search of the NCBI wheat EST database of over 420,000 cDNA sequences revealed that 1,143 of the predicted rice genes (38.9%) have significant homology to wheat ESTs (bit score >/= 100). Further BLASTN search of these 1,143 rice genes with the GrainGenes database of sequence contigs containing bin-mapped wheat ESTs allowed 113 of the genes to be placed in bins located on wheat chromosomes of different homoeologous groups. The largest number of genes, about one-third, mapped to the homoeologous group 4 chromosomes of wheat, suggesting a common evolutionary origin. The remaining genes were located on wheat chromosomes of different groups with significantly higher numbers for groups 3 and 5. Location of bin-mapped wheat contigs to chromosomes of all the seven homoeologous groups can be ascribed to movement of genes (transpositions) or chromosome segments (translocations) within rice or the hexaploid wheat genomes. Alternatively, it could be due to ancient duplications in the common ancestral genome of wheat and rice followed by selective elimination of genes in the wheat and rice genomes. While there exists definite conservation of gene sequences and the ancestral chromosomal identity between rice and wheat, there is no obvious conservation of the gene order at this level of resolution. Lack of extensive colinearity between rice and wheat genomes suggests that there have been many insertions, deletions, duplications and translocations that make the synteny comparisons much more complicated than earlier thought. However, enhanced resolution of comparative sequence analysis may reveal smaller conserved regions of colinearity, which will facilitate selection of markers for saturation mapping and sequencing of the gene-rich regions of the wheat genome.

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Year:  2004        PMID: 15085449     DOI: 10.1007/s10142-004-0109-y

Source DB:  PubMed          Journal:  Funct Integr Genomics        ISSN: 1438-793X            Impact factor:   3.410


  19 in total

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  25 in total

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Journal:  Funct Integr Genomics       Date:  2004-04-30       Impact factor: 3.410

Review 2.  Molecular markers from the transcribed/expressed region of the genome in higher plants.

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3.  Transcriptome analysis of salinity stress responses in common wheat using a 22k oligo-DNA microarray.

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Review 4.  The bioinformatics challenges in comparative analysis of cereal genomes-an overview.

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5.  The PDI genes of wheat and their syntenic relationship to the esp2 locus of rice.

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8.  Single-copy genes define a conserved order between rice and wheat for understanding differences caused by duplication, deletion, and transposition of genes.

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