Several DNA-damage detection and repair mechanisms have evolved to repair double-strand breaks induced by mutagens. Later in evolutionary history, DNA single- and double-strand cuts made possible immune diversity by V(D)J recombination and recombination at meiosis. Such cuts are induced endogenously
The social evolution of somatic fusion
β Scribed by Duur K. Aanen; Alfons J.M. Debets; J. Arjan G.M. de Visser; Rolf F. Hoekstra
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 164 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0265-9247
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
The widespread potential for somatic fusion among different conspecific multicellular individuals suggests that such fusion is adaptive. However, because recognition of nonβkin (allorecognition) usually leads to a rejection response, successful somatic fusion is limited to close kin. This is consistent with kinβselection theory, which predicts that the potential cost of fusion and the potential for somatic parasitism decrease with increasing relatedness. Paradoxically, however, Crozier1 found that, in the short term, positiveβfrequencyβdependent selection eliminates the required genetic polymorphism at allorecognition loci. The βCrozier paradoxβ may be solved if allorecognition is based on extrinsically balanced polymorphisms, for example at immune loci. Alternatively, the assumption of most models that self fusion is mutually beneficial is wrong. If fusion is on average harmful, selection will promote unconditional rejection. However, we propose that fusion within individuals is beneficial, selecting for the ability to fuse, but fusion between individuals on average costly, selecting for nonβself recognition (rather than nonβkin recognition). We discuss experimental data on fungi that are consistent with this hypothesis. BioEssays 30:1193β1203, 2008. Β© 2008 Wiley Periodicals, Inc.
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