Last Updated: 28/11/2025

Female-specific gene regulation in malaria parasites by an AP2-family transcription factor

Objectives

*Original title and text were machine translated from Japanese

This project aims to understand if the AP2-family transcription factor AP2-F is crucial for female-specific gene regulation in malaria parasites, specifically in Plasmodium berghei.

Principal Institution

Mie University, Japan

Principal Investigators / Focal Persons

Izumi Kaneko

Rationale and Abstract

The malarial gametocyte, the gamete precursor, is the parasite stage obligatory for malarial transmission to the mosquito vector. It is reported that an AP2-family transcription factor, AP2-F, is responsible for female-specific gene regulation. AP2-F expression in Plasmodium berghei was observed exclusively in female gametocytes. AP2-F disruption resulted in the arrest of female maturation, but did not affect the development of males. ChIP-seq analysis showed that AP2-FG directly regulates over 750 genes. Its targets include genes for female gametocyte-specific functions, such as gametogenesis, fertilization, and zygote development. AP2-F binding to target gene promoters was associated with a 10-bp sequence motif. These results indicate that AP2-F plays a role in the differentiation of early gametocytes into mature females by governing a female-specific gene expression repertoire.

Date

Apr 2016 — Mar 2019

Total Project Funding

$43,542

Funding Details
Country / Project Site(s)

Japan

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