cis-regulatory elements (CREs) are regions of non-coding DNA which regulate the transcription of nearby genes. The Latin prefix cis translates to “on this side”. CREs are found in the vicinity of the gene, or genes, they regulate. CREs typically regulate gene transcription by functioning as binding sites for transcription factors.
The genome of an organism contains anywhere from a few hundred to thousands of different genes, all encoding a singular product or more. For numerous reasons, including organizational maintenance, energy conservation, and generating phenotypic variance, it is important that genes are only expressed when they are needed. The most efficient way for an organism to regulate genetic expression is at the transcriptional level. CREs function to control transcription by acting nearby or within a gene. The most well characterized types of CREs are enhancers and promoters. Both of these sequence elements are structural regions of DNA that serve as transcriptional regulators.
Promoters are relatively short sequences of DNA, approximately 40 base pairs (bp), usually located upstream of a transcription start site. This regulatory region includes the site where transcription is initiated and the region approximately 35 bp upstream or downstream from the initiation site. Promoters usually have the following four components: the TATA box, a TFIIB recognition site, an initiator, and the downstream core promoter element. Interestingly, it has been found that a single gene can contain multiple promoter sites. In order to initiate transcription of the downstream gene, a host of DNA-binding proteins called transcription factors (TFs) must bind sequentially to this region. Only once this region has been bound with the appropriate set of TFs, and in the proper order, can RNA polymerase bind and begin transcribing the gene. Contrastingly, enhancers influence transcription of genes on the same molecule of DNA and can be found upstream, downstream, within the introns, or even relatively far away from the gene they regulate. Multiple enhancers can act in a coordinated fashion to regulate transcription of one gene.
CREs have an important evolutionary role. The coding regions of genes are often well conserved among organisms; yet different organisms display marked phenotypic diversity. It has been found that polymorphisms occurring within non-coding sequences have a profound effect on phenotype by altering gene expression. Mutations arising within a CRE can generate expression variance by changing the way TFs bind. Tighter or looser binding of regulatory proteins will lead to up- or down-regulated transcription.
An example of a cis-acting regulatory sequence is the operator in the lac operon. This DNA sequence is bound by the lac repressor, which, in turn, prevents transcription of the adjacent genes on the same DNA molecule. The lac operator is, thus, considered to "act in cis" on the regulation of the nearby genes. The operator itself does not code for any protein or RNA.
In contrast, trans-regulatory elements are diffusible factors, usually proteins, that may modify the expression of genes distant from the gene that was originally transcribed to create them. For example, a transcription factor that regulates a gene on chromosome 6 might itself have been transcribed from a gene on chromosome 11. The term trans-regulatory is constructed from the Latin root trans, which means "across from".
To summarize, cis-regulatory elements are present on the same molecule of DNA as the gene they regulate whereas trans-regulatory elements can regulate genes distant from the gene from which they were transcribed.
Examples in RNA
|Frameshift element||Regulates alternative frame use with messenger RNAs||Archaea, bacteria, Eukaryota, RNA viruses|||
|Internal ribosome entry site||IRES||Initiates translation in the middle of a messenger RNA||RNA virus, Eukaryota|||
|Iron response element||IRE||Regulates the expression of iron associated genes||Eukaryota|||
|Leader peptide||Regulates transcription of associated genes and/or operons||Bacteria|||
|Pyrrolysine insertion sequence||PYLIS||Directs the cell to translate immediately adjacent UAG stop codons into pyrrolysine||Archaea|||
|Riboswitch||Gene regulation||Bacteria, Eukaryota|||
|RNA thermometer||Gene regulation||Bacteria|||
|Selenocysteine insertion sequence||SECIS||Directs the cell to translate UGA stop-codons as selenocysteines||Metazoa|||
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