Premium
Transpositional shuffling and quality control in male germ cells to enhance evolution of complex organisms
Author(s) -
Werner Andreas,
Piatek Monica J.,
Mattick John S.
Publication year - 2015
Publication title -
annals of the new york academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.712
H-Index - 248
eISSN - 1749-6632
pISSN - 0077-8923
DOI - 10.1111/nyas.12608
Subject(s) - shuffling , biology , dna shuffling , germ , quality (philosophy) , control (management) , evolutionary biology , genetics , computational biology , computer science , directed evolution , microbiology and biotechnology , artificial intelligence , gene , mutant , philosophy , epistemology , programming language
Complex organisms, particularly mammals, have long generation times and produce small numbers of progeny that undergo increasingly entangled developmental programs. This reduces the ability of such organisms to explore evolutionary space, and, consequently, strategies that mitigate this problem likely have a strategic advantage. Here, we suggest that animals exploit the controlled shuffling of transposons to enhance genomic variability in conjunction with a molecular screening mechanism to exclude deleterious events. Accordingly, the removal of repressive DNA‐methylation marks during male germ cell development is an evolved function that exploits the mutagenic potential of transposable elements. A wave of transcription during the meiotic phase of spermatogenesis produces the most complex transcriptome of all mammalian cells, including genic and noncoding sense–antisense RNA pairs that enable a genome‐wide quality‐control mechanism. Cells that fail the genomic quality test are excluded from further development, eventually resulting in a positively selected mature sperm population. We suggest that these processes, enhanced variability and stringent molecular quality control, compensate for the apparent reduced potential of complex animals to adapt and evolve.