Abstract
Assigning functions to genes is one of the major challenges of the post-genomic era. Usually, functions are assigned based on similarity of the coding sequences to sequences of known genes, or by identification of transcriptional cis-regulatory elements that are known to be associated with specific pathways or conditions. In trypanosomatids, where regulation of gene expression takes place mainly at the post-transcriptional level, new approaches for function assignment are needed. Here we demonstrate the identification of novel S-phase expressed genes in Leishmania major, based on a post-transcriptional control element that was recognized in Crithidia fasciculata as involved in the cell cycle-dependent expression of several nuclear and mitochondrial S-phase expressed genes. Hypothesizing that a similar regulatory mechanism is manifested in L.major, we have applied a computational search for similar control elements in the genome of L.major. Our computational scan yielded 132 genes, of which 33% are homologues of known DNA metabolism genes and 63% lack any annotation. Experimental testing of seven of these genes revealed that their mRNAs cycle throughout the cell cycle, reaching a maximum level during S-phase or just prior to it. It is suggested that screening for post-transcriptional control elements associated with a specific function provides an efficient method for assigning functions to trypanosomatid genes.
Original language | English |
---|---|
Pages (from-to) | 4235-4242 |
Number of pages | 8 |
Journal | Nucleic Acids Research |
Volume | 33 |
Issue number | 13 |
DOIs | |
State | Published - 2005 |
Externally published | Yes |
Bibliographical note
Funding Information:This study was supported, in parts, by grant No. 623 from the Israel Science Foundation (ISF) and by grant No. 2001006 from the United State-Israel Binational Science Foundation (BSF), Jerusalem, Israel. I.O. was supported by a Yeshaya Horowitz Fellowship. Funding to pay the Open Access publication charges for this article was provided by grant No. 623 from the Israel Science Foundation.
Funding
This study was supported, in parts, by grant No. 623 from the Israel Science Foundation (ISF) and by grant No. 2001006 from the United State-Israel Binational Science Foundation (BSF), Jerusalem, Israel. I.O. was supported by a Yeshaya Horowitz Fellowship. Funding to pay the Open Access publication charges for this article was provided by grant No. 623 from the Israel Science Foundation.
Funders | Funder number |
---|---|
United States-Israel Binational Science Foundation | |
Israel Science Foundation | 2001006 |