Knockdown of the Plasmodium falciparum SURFIN4.1 antigen leads to an increase of its cognate transcript

PLoS One. 2017 Aug 11;12(8):e0183129. doi: 10.1371/journal.pone.0183129. eCollection 2017.

Abstract

The genome of the malaria parasite Plasmodium falciparum contains the surf gene family which encodes large transmembrane proteins of unknown function. While some surf alleles appear to be expressed in sexual stages, others occur in asexual blood stage forms and may be associated to virulence-associated processes and undergo transcriptional switching. We accessed the transcription of surf genes along multiple invasions by real time PCR. Based on the observation of persistent expression of gene surf4.1, we created a parasite line which expresses a conditionally destabilized SURFIN4.1 protein. Upon destabilization of the protein, no interference of parasite growth or morphological changes were detected. However, we observed a strong increase in the transcript quantities of surf4.1 and sometimes of other surf genes in knocked-down parasites. While this effect was reversible when SURFIN4.1 was stabilized again after a few days of destabilization, longer destabilization periods resulted in a transcriptional switch away from surf4.1. When we tested if a longer transcript half-life was responsible for increased transcript detection in SURFIN4.1 knocked-down parasites, no alteration was found compared to control parasite lines. This suggests a specific feedback of the expressed SURFIN protein to its transcript pointing to a novel type of regulation, inedited in Plasmodium.

MeSH terms

  • Alleles
  • Antigens, Protozoan / genetics*
  • Antigens, Protozoan / metabolism
  • Cloning, Organism
  • Erythrocytes / parasitology
  • Feedback, Physiological*
  • Gene Expression Regulation
  • Gene Knockdown Techniques
  • Half-Life
  • Humans
  • Life Cycle Stages / genetics*
  • Morpholines / pharmacology
  • Plasmodium falciparum / genetics*
  • Plasmodium falciparum / growth & development
  • Plasmodium falciparum / metabolism
  • Protein Isoforms / antagonists & inhibitors
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • RNA Stability
  • RNA, Messenger / agonists
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism
  • Transfection

Substances

  • Antigens, Protozoan
  • Morpholines
  • Protein Isoforms
  • RNA, Messenger
  • Shield-1 compound

Grants and funding

This work was supported by FAPESP grant 2012/23306-5 and 2015/17174-7 (GW), a FAPESP master fellowship to TMS (2013/12439-7) and grants to MFA (2009/51026-4, 2015/19316-3). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.