Evolutionarily dynamic roles of a PUF RNA-binding protein in the somatic development of Caenorhabditis briggsae.
Evolutionarily dynamic roles of a PUF RNA-binding protein in the somatic development of Caenorhabditis briggsae.
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PUF RNA 结合蛋白在 Caenorhabditis briggsae 体细胞发育中的进化动态作用。
DOI:
10.1002/jez.b.22550
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发表时间:
2014
期刊:
影响因子:
--
通讯作者:
Haag,EricS
中科院分区:
文献类型:
--
作者:
Liu,Qinwen;Haag,EricS
Gene duplication and divergence has emerged as an important aspect of developmental evolution. The genomes ofCaenorhabditisnematodes encode an ancient family of PUF RNA‐binding proteins. Most have been implicated in germline development, and are often redundant with paralogs of the same sub‐family. An exception isCbr‐puf‐2(one of threeCaenorhabditis briggsaePUF‐2 sub‐family paralogs), which is required for development past the second larval stage. Here, we provide a detailed functional characterization ofCbr‐puf‐2. The larval arrest ofCbr‐puf‐2mutant animals is caused by inefficient breakdown of bacterial food, which leads to starvation.Cbr‐puf‐2is required for the normal grinding cycle of the muscular terminal bulb during early larval stages, and is transiently expressed in this tissue. In addition, rescue of larval arrest reveals thatCbr‐puf‐2also promotes normal vulval development. It is expressed in the anchor cell (which induces vulval fate) and vulval muscles, but not in the vulva precursor cells (VPCs) themselves. This contrasts with the VPC‐autonomous repression of vulval development described for theCaenorhabditis eleganshomologsfbf‐1/2. These different roles for PUF proteins occur even as the vulva and pharynx maintain highly conserved anatomies acrossCaenorhabditis, indicating pervasive developmental system drift (DSD). Because Cbr‐PUF‐2 shares RNA‐binding specificity with its paralogs and withC. elegansFBF, we suggest that functional novelty of RNA‐binding proteins evolves through changes in the site of their expression, perhaps in concert withcis‐regulatory evolution in target mRNAs.J. Exp. Zool. (Mol. Dev. Evol.) 322B: 129–141, 2014. © 2013 Wiley Periodicals, Inc.