RNase P RNA from the Recently Evolved Plastid of Paulinella and from Algae

International Journal of Molecular Sciences

Pilar Bernal-Bayard²  Leonor Puerto-Galán²  Agustín Vioque¹ 

[1] Instituto de Bioquímica Vegetal y Fotosíntesis, Universidad de Sevilla and CSIC, Américo Vespucio 49, 41092 Sevilla, Spain;

关键词: chloroplast evolution;    chromatophore;    cyanobacteria;    RNase P;    tRNA processing;   

DOI  :  10.3390/ijms151120859

来源: mdpi

【 摘 要 】

The RNase P RNA catalytic subunit (RPR) encoded in some plastids has been found to be functionally defective. The amoeba Paulinella chromatophora contains an organelle (chromatophore) that is derived from the recent endosymbiotic acquisition of a cyanobacterium, and therefore represents a model of the early steps in the acquisition of plastids. In contrast with plastid RPRs the chromatophore RPR retains functionality similar to the cyanobacterial enzyme. The chromatophore RPR sequence deviates from consensus at some positions but those changes allow optimal activity compared with mutated chromatophore RPR with the consensus sequence. We have analyzed additional RPR sequences identifiable in plastids and have found that it is present in all red algae and in several prasinophyte green algae. We have assayed in vitro a subset of the plastid RPRs not previously analyzed and confirm that these organelle RPRs lack RNase P activity in vitro.

【 授权许可】

CC BY   
© 2014 by the authors; licensee MDPI, Basel, Switzerland.