Transposable Element- driven Duplications during Hominoid Genome Evolution
نویسنده
چکیده
p0001 Akin to any large texts in a natural language, hominoid genomes appear as palimpsests ofmorphemes, lexemes and other lexical modules, each with its own structure, distribution and fluctuating copy numbers (Zhou and Mishra, 2004; Thomas et al., 2004). Duplication appears to be one of the main mechanisms in shaping and reshaping this genomic architecture. Duplication occurs at multiple scales, ranging at one end from small local tandem repeats that are the results of polymerase slippage or unequal crossing-over, to the duplication of a whole genome at the other extreme. Segmental duplication (SD)occurs at a scale between small repeats and thewhole genome.Duplications provide the genome with additional and (initially) redundant copies of genes and their regulatory elements, thus initiating gene family expansion and offering the species adequate freedom to explore new functionality and develop more refined regulations (Armengol, 2005; Cheng, 2005) AU:2 . Duplication promotes a faster and more complex dynamics during genome evolution – the duplicated sequences can serve as the homologous region for further recombination events, which can lead to further duplication, deletion and other rearrangement events (Zhou and Mishra, 2004). As was found in the subtelomeric and pericentromeric regions of the mammalian genomes, SDs in such regions generate a complicated pattern of recursively nested events and creates a fertile breeding ground for novel functional elements. Years before the genomic era tools had pinpointed the duplicatedmotifs in genomes, in a surprisingly prescient thesis, SOhno had already suggested a possible reciprocative roles between duplications and selections in the evolutionary dynamics, as he noted that ‘Natural selection merely modified while redundancy created’ (Ohno, 1970) AU:3 .
منابع مشابه
Serial segmental duplications during primate evolution result in complex human genome architecture.
The human genome is particularly rich in low-copy repeats (LCRs) or segmental duplications (5%-10%), and this characteristic likely distinguishes us from lower mammals such as rodents. How and why the complex human genome architecture consisting of multiple LCRs has evolved remains an open question. Using molecular and computational analyses of human and primate genomic regions, we analyzed the...
متن کاملHominoid fission of chromosome 14/15 and the role of segmental duplications.
Ape chromosomes homologous to human chromosomes 14 and 15 were generated by a fission event of an ancestral submetacentric chromosome, where the two chromosomes were joined head-to-tail. The hominoid ancestral chromosome most closely resembles the macaque chromosome 7. In this work, we provide insights into the evolution of human chromosomes 14 and 15, performing a comparative study between mac...
متن کاملIdentification and Characterisation of five novel Miniature Inverted-repeat Transposable Elements (MITEs) in amphioxus (Branchiostoma floridae)
As the sister group to vertebrates, amphioxus is consistently used as a model of genome evolution for understanding the invertebrate/vertebrate transition. The amphioxus genome has not undergone massive duplications like those in the vertebrates or disruptive rearrangements like in the genome of Ciona, a urochordate, making it an ideal evolutionary model. Transposable elements have been linked ...
متن کاملZBED Evolution: Repeated Utilization of DNA Transposons as Regulators of Diverse Host Functions
ZBED genes originate from domesticated hAT DNA transposons and encode regulatory proteins of diverse function in vertebrates. Here we reveal the evolutionary relationship between ZBED genes and demonstrate that they are derived from at least two independent domestication events in jawed vertebrate ancestors. We show that ZBEDs form two monophyletic clades, one of which has expanded through seve...
متن کاملRecurrent duplication-driven transposition of DNA during hominoid evolution.
The underlying mechanism by which the interspersed pattern of human segmental duplications has evolved is unknown. Based on a comparative analysis of primate genomes, we show that a particular segmental duplication (LCR16a) has been the source locus for the formation of the majority of intrachromosomal duplications blocks on human chromosome 16. We provide evidence that this particular segment ...
متن کامل