Abstract
Leishmania differentiates from the promastigote to the amastigote stage during its digenetic life cycle. Characterization of the developmentally regulated genes during that process would help to elucidate the mechanisms of gene regulation. In this study, specific fragments of mRNAs from the amastigote stage of L. mexicana mexicana were discriminated from those of the promastigote and metacyclic stages by differential display. This technique combined with spliced-leader polymerase chain reaction allowed isolation of the complete gene VG7A5. The sequence of this gene did not align with any published L. mexicana sequence. More than one copy of this gene was identified in the genome by Southern-blot analysis and was transcribed exclusively in the amastigote stage. At 20 bp upstream from the splice AG site it has a trans-splicing polypyrimidine tract. The gene encodes the subcellular localization motifs 5′-GGACT and AAGCT-3′ in the 3′ untranslated region of the mRNA. The open reading frame of the gene VG7A5 predicts a polypeptide of 587 amino acid residues that has a KGRR amidation motif near its carboxyl terminus, suggesting that in the mammalian host this protein may be involved in the process of acute inflammation.
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Received: 24 June 1999 / Accepted: 10 September 1999
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Liu, K., Zinker, S., Argüello, C. et al. Isolation and analysis of a new developmentally regulated gene from amastigotes of Leishmania mexicana mexicana . Parasitol Res 86, 140–150 (2000). https://doi.org/10.1007/s004360050023
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DOI: https://doi.org/10.1007/s004360050023