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Abstract
Background: Transmission of the malaria parasite Plasmodium falciparum from humans to the mosquito vector
requires differentiation of a sub-population of asexual forms replicating within red blood cells into non-dividing male
and female gametocytes. The nature of the molecular mechanism underlying this key differentiation event required
for malaria transmission is not fully understood.
Methods: Whole genome sequencing was used to examine the genomic diversity of the gametocyte non-producing
3D7-derived lines F12 and A4. These lines were used in the recent detection of the PF3D7_1222600 locus (encoding
PfAP2-G), which acts as a genetic master switch that triggers gametocyte development.
Results: The evolutionary changes from the 3D7 parental strain through its derivatives F12 (culture-passage derived
cloned line) and A4 (transgenic cloned line) were identified. The genetic differences including the formation of chimeric
var genes are presented. Conclusion: A genomics resource is provided for the further study of gametocytogenesis or other phenotypes using
these parasite lines.
Original language | English |
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Number of pages | 10 |
Journal | Malaria Journal |
Volume | 15 |
Issue number | 229 |
DOIs | |
Publication status | Published - 21 Apr 2016 |
Keywords / Materials (for Non-textual outputs)
- Gametocytes
- Plasmodium falciparum
- A4
- F12
- ApiAP2 gene family
- Whole genome sequencing
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Dive into the research topics of 'Genomic variation in two gametocyte non-producing Plasmodium falciparum clonal lines'. Together they form a unique fingerprint.Projects
- 1 Finished
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THE MANAGEMENT OF METRICS : PERFORMANCE MEASURES IN THE PUBLIC SECTOR
Townley, B.
1/01/04 → 31/12/04
Project: Research