Life Science and Technology News

Understanding the Regulation of Apicoplast Gene Expression in the Malaria Parasite

July 14, 2023

Gene expression within the apicoplast, an organelle in the malaria parasite Plasmodium falciparum, is regulated by melatonin (the circadian signaling hormone) in host blood, and intrinsic parasite cues, via a factor called ApSigma, as identified by a recent study aided by Tokyo Tech's World Research Hub Initiative. The regulatory system highlighted in this study might be a future target for malaria treatment.

Malaria is one of the biggest public health risks, with around 240 million people from across the globe contracting it every year. However, this life-threatening disease is not contagious. It is transmitted by the bite of a female Anopheles mosquito infected with the malaria parasite, Plasmodium falciparum (Figure 1)
. This parasite enters the human body through the mosquito bite and causes symptoms like fever, cold, fatigue, and headache, which are highly periodic. The periodicity of symptoms can be linked to the synchronization of the parasite's life cycle with the circadian rhythm—i.e., the 24-hour internal biological clock—of the infected person or the host.

Figure 1 A female Anopheles mosquito Malaria, transmitted by mosquito bites, is still a serious infectious disease that kills many people (image courtesy of Assistant Professor Kyoko Futami, Nagasaki University).

Figure 1. A female Anopheles mosquito

Malaria, transmitted by mosquito bites, is still a serious infectious disease that kills many people (image courtesy of Assistant Professor Kyoko Futami, Nagasaki University).

P. falciparum contains an apicoplast, a unique cellular organelle which contains its own genome and is crucial for the parasite's life cycle. Despite its importance, however, not much is known about the mechanisms regulating gene expression in apicoplasts and their potential role in modulating the observed periodicity of malaria symptoms, or the life cycle of P. falciparum. This is why recently, a team of scientists led by Professor Kan Tanaka, of Tokyo Institute of Technology (Tokyo Tech), undertook a joint research project to take a closer look at the underlying mechanisms that mediate apicoplast gene expression. The work, published in Proceedings of National Academy of Sciences of United States of America (PNAS), was a result of collaboration with co-authors Professor Kiyoshi Kita of Nagasaki University and Professor Antony N. Dodd, a group leader at the John Innes Centre in the UK—also a visiting professor at Tokyo Tech—facilitated by the institute's World Research Hub Initiative (WRHI), a project for interdisciplinary collaboration with leading researchers from across the world.

"Previous studies have shown that certain plant σ subunits participate in the circadian regulation of gene expression in plastids (i.e., organelles like the apicoplast). Therefore, the present study hypothesized that a nuclear-encoded σ subunit might coordinate apicoplast gene expression with the life cycle of P. falciparum or the circadian rhythm of its host," explains Prof. Tanaka.

The team cultured P. falciparum in a lab and studied it using phylogenetic analysis and immunofluorescence microscopy techniques. As a result, they identified ApSigma, a nuclear encoded apicoplast RNA polymerase σ subunit. It, along with the α subunit, likely mediates apicoplast transcript accumulation, whose periodicity is akin to that of the parasite's developmental control. In addition, apicoplast transcription and expression of the apicoplast subunit gene, apSig, increased in the presence of melatonin, the circadian signaling hormone present in host blood.

Based on the data collected from different tests, the scientists suggest that there is an evolutionarily preserved regulatory system in which the host's circadian rhythm is integrated with the parasite's intrinsic cues. Together, they coordinate genome transcription in the apicoplast of P. falciparum. This work lays solid groundwork for further studies in the field aiming to comprehensively explain the regulatory mechanisms of Plasmodium's cell cycle.

In conclusion, Prof. Tanaka highlights the future implications of the present research. "Malaria kills hundreds of thousands of people across the world, every year. This study identifies a regulatory system that might be a future target for malaria treatment."

Professor Dodd, adds to that, "It is amazing that a process we identified in plants has led to the discovery of an equivalent mechanism in a globally important pathogen. The new protein and mechanism identified could present a new target for the development of drugs for the treatment and or prevention of malaria, in both humans and farm animals."

Professor Kita signs off on a positive note. "This research demonstrates the value of international and interdisciplinary collaboration, and the power of plant sciences and microbiology to drive unusual and novel discoveries that could be of considerable global benefit," he says.

Here's hoping for efficient treatment of malaria!

Reference

Authors :	Yuki Kobayashi¹, Keisuke Komatsuya^2,3, Sousuke Imamura^1,4, Tomoyoshi Nozaki², Yoh-ichi Watanabe², Shigeharu Sato^1,5,6,7, Antony N. Dodd⁸, Kiyoshi Kita^2,7,9, and Kan Tanaka¹
Title :	Coordination of apicoplast transcription in a malaria parasite by internal and host cues
Journal :	Proceedings of National Academy of Sciences of United States of America (PNAS)
DOI :	10.1073/pnas.2214765120
Affiliations :	¹Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology ²Department of Biomedical Chemistry, Graduate School of Medicine, The University of Tokyo ³Laboratory of Biomembrane, Tokyo Metropolitan Institute of Medical Science ⁴Space Environment and Energy Laboratories, Nippon Telegraph and Telephone Corporation ⁵Department of Pathology and Microbiology, Faculty of Medicine and Health Sciences, Universiti Malaysia Sabah ⁶Borneo Medical and Health Research Centre, Faculty of Medicine and Health Sciences, Universiti Malaysia Sabah ⁷School of Tropical Medicine and Global Health, Nagasaki University ⁸Department of Cell and Developmental Biology, John Innes Centre ⁹Department of Host-Defense Biochemistry, Institute of Tropical Medicine, Nagasaki University