Leader sequences

The 5 leader in eukaryotic mRNA is defined as the sequence between the cap and the AUG initiation codon. The most striking 

Another common sequence of the leader of eukaryotic mRNA is CUUPyUG (Baralle and Brownlee, 1978), found in p-like globin mRNA at seven nucleotides downstream from the cap (Efstratiadis et al., 1980). Conserved sequences close to the cap may, however, form part of the promoter for transcription (Talkington and Leder, 1982). 

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The maturation of proteins into their final structural state often involves the cleavage or formation (or both) of covalent bonds, a process termed posttranslational modification. Many polypeptides are initially synthesized as larger precursors, called proproteins. The extra polypeptide segments in these proproteins often serve as leader sequences that target a polypeptide... 

Matrix proteins must pass from cytosolic polyribosomes through the outer and inner mitochondrial membranes to reach their destination. Passage through the two membranes is called translocation. They have an amino terminal leader sequence (presequence),... 

The capped leader sequence of the brome mosaic virus mRNA, an oligonucleotide 5 triphosphate, has been synthesized analogously by reaction of an oligoribonucleotide 5 -phosphoric imidazolide. 951... 

Foreign protein Culture type Plant species Transformation method Promoter Leader sequence Production level (maximum) Reference... 

Alterations to the proteins and pre-proteins expressed by cultured plant cells have been used to facilitate product recovery. A leader sequence is required for foreign protein secretion from plant cells into the apoplast and then into the culture medium. As indicated in Table 2.1, plant, mammalian and viral sequences have been employed to achieve the entry of transgenic proteins into the bulk-flow pathway in plant cultures. 

Human serum albumin CaMVenhanced 35S promoter/ A1MV RNA synthetic leader sequence/nos terminator Native or PR-S leader peptide S. tuberosum (leaves) 0.02% ofTSP 48... 

Based on the intrinsic mitochondriotropism of dequalinium and its unique self-assembly behavior, we have developed a strategy for direct mitochondrial transfection (47-49), which involves the transport of a DNA-mitochondrial leader sequence (MLS) peptide conjugate to mitochondria using DQAsomes, the liberation of this conjugate from the cationic vector upon contact with the mitochondrial outer membrane followed by DNA uptake via the mitochondrial protein import machinery. We have demonstrated that DQAsomes fulfill all essential prerequisites for a mitochondria-specific DNA delivery system they bind and condense pDNA (24), protect it from... 

Figure 4 The biosynthesis of nisin A as a representative example of the posttranslational maturation process of lantibiotics. Following ribosomal synthesis, NisB dehydrates serine and threonine residues in the structural region of the prepeptide NisA. NisC subsequently catalyzes intramolecular addition of cysteine residues onto the dehydro amino acids in a stereo- and regioselective manner. Subsequent transport of the final product across the cell membrane by NisT and proteolytic cleavage of the leader sequence by NisP produces the mature lantibiotic. For the sequence of the leader peptide, see Figure 6. Adapted with permission from J. M. Willey W. A. van der Donk, Annu. Rev. Microbiol. 2007, 61, 477-501.

Figure 6 Sequence alignment of lantibiotic and nonlantibiotic bacteriocin prepeptides. The residues in red indicate those positions that are fully conserved within that class, and those in blue are highly conserved. For the nonlantibiotic bacteriocins, only the leader sequences are shown. The site of proteolysis is indicated by the arrow. For cytolysin, the additional six residues removed by CylA are indicated in green.

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