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Gene Arrays atPneumocystis cariniiTelomeres
Author(s) -
Scott P. Keely,
Hubert Renauld,
Ann E. Wakefield,
Melanie T. Cushion,
A. George Smulian,
Nigel Fosker,
Audrey Fraser,
David Harris,
Lee Murphy,
Claire Price,
Michael A. Quail,
Kathy Seeger,
Sarah Sharp,
Carolyn J. Tindal,
Tim Warren,
Eduard Zuiderwijk,
B. G. Barrell,
James R. Stringer,
Neil Hall
Publication year - 2005
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1534/genetics.105.040733
Subject(s) - biology , genetics , gene , subtelomere , pneumocystis carinii , gene family , gene conversion , gene duplication , antigenic variation , genome , gene cluster , virology , human immunodeficiency virus (hiv) , pneumocystis jirovecii
In the fungus Pneumocystis carinii, at least three gene families (PRT1, MSR, and MSG) have the potential to generate high-frequency antigenic variation, which is likely to be a strategy by which this parasitic fungus is able to prolong its survival in the rat lung. Members of these gene families are clustered at chromosome termini, a location that fosters recombination, which has been implicated in selective expression of MSG genes. To gain insight into the architecture, evolution, and regulation of these gene clusters, six telomeric segments of the genome were sequenced. Each of the segments began with one or more unique genes, after which were members of different gene families, arranged in a head-to-tail array. The three-gene repeat PRT1-MSR-MSG was common, suggesting that duplications of these repeats have contributed to expansion of all three families. However, members of a gene family in an array were no more similar to one another than to members in other arrays, indicating rapid divergence after duplication. The intergenic spacers were more conserved than the genes and contained sequence motifs also present in subtelomeres, which in other species have been implicated in gene expression and recombination. Long mononucleotide tracts were present in some MSR genes. These unstable sequences can be expected to suffer frequent frameshift mutations, providing P. carinii with another mechanism to generate antigen variation.

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