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Turkish Journal of Biology

DOI

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Abstract

Expressed sequence tag (EST) technology has spurred targeting the functional portion of genomes for several organisms. Constructed redundant complementary DNA (cDNA) libraries have targeted a majority of constitutive and over-expressed genes. However, the majority of lowly expressed and un-induced genes have not been able to be easily tagged and cloned. The objective of this study was to clone low and rarely expressed transcripts in wheat. Using a combination of a polyacrylamide gel and a motif-based PCR amplification, we cloned 144 bands containing 189 wheat fragments. Sequence analysis revealed 74 contigs, of which only 22 being present in database. The remaining 52 were unique, and were not present in any public EST or non-redundant database. Compared to 5% efficiency in the public EST database, the efficiency of cloning of unique sequences was about 28%. Therefore, the approach we describe here is highly promising for targeting the rarely and lowly expressed genes in wheat and, probably, various other genomes.

First Page

7

Last Page

13

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