| Autor: |
LAPP, S. A., GERALDO, J. A., CHIEN, J.-T., AY, F., PAKALA, S. B., BATUGEDARA, G., HUMPHREY, J., DeBARRY, J. D., Le ROCH, K. G., GALINSKI, M. R., KISSINGER, J. C. |
| Předmět: |
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| Zdroj: |
Parasitology; Jan2018, Vol. 145 Issue 1, p71-84, 14p |
| Abstrakt: |
Plasmodium knowlesi has risen in importance as a zoonotic parasite that has been causing regular episodes of malaria throughout South East Asia. The P. knowlesi genome sequence generated in 2008 highlighted and confirmed many similarities and differences in Plasmodium species, including a global view of several multigene families, such as the large SICAvar multigene family encoding the variant antigens known as the schizont-infected cell agglutination proteins. However, repetitive DNA sequences are the bane of any genome project, and this and other Plasmodium genome projects have not been immune to the gaps, rearrangements and other pitfalls created by these genomic features. Today, long-read PacBio and chromatin conformation technologies are overcoming such obstacles. Here, based on the use of these technologies, we present a highly refined de novo P. knowlesi genome sequence of the Pk1(A+) clone. This sequence and annotation, referred to as the 'MaHPIC Pk genome sequence', includes manual annotation of the SICAvar gene family with 136 fulllength members categorized as type I or II. This sequence provides a framework that will permit a better understanding of the SICAvar repertoire, selective pressures acting on this gene family and mechanisms of antigenic variation in this species and other pathogens. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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