Signal Recognition Particle RNA in Dinoflagellates and the Perkinsid Perkinsus marinus

• In dinoflagellates and perkinsids, the molecular structure of the protein translocating machinery is unclear. Here, we identified several types of full-length signal recognition particle (SRP) RNA genes from Karenia brevis (dinoflagellate) and Perkinsus marinus (perkinsid). We also identified the four SRP S-domain proteins, but not the two Alu domain proteins, from P. marinus and several dinoflagellates. We mapped both ends of SRP RNA transcripts from K. brevis and P. marinus, and obtained the 3' end from four other dinoflagellates. The lengths of SRP RNA are predicted to be similar to 260-300 nt in dinoflagellates and 280-285 nt in P. marinus. Although these SRP RNA sequences are substantially variable, the predicted structures are similar. The genomic organization of the SRP RNA gene differs among species. In K. brevis, this gene is located downstream of the spliced leader (SL) RNA, either as SL RNA-SRP RNA-tRNA gene tandem repeats, or within a SL RNA-SRP RNA-tRNA-U6-5S rRNA gene cluster. In other dinoflagellates, SRP RNA does not cluster with SL RNA or 5S rRNA genes. The majority of P. marinus SRP RNA genes array as tandem repeats without the above-mentioned small RNA genes. Our results capture a snapshot of a potentially complex evolutionary history of SRP RNA in alveolates. (c) 2013 Elsevier GmbH. All rights reserved.

Ämnesord

NATURVETENSKAP  -- Biologi (hsv//swe)

NATURAL SCIENCES  -- Biological Sciences (hsv//eng)

Nyckelord

Dinoflagellates

Perkinsus marinus

SRP RNA

protein translocation

SPLICED LEADER RNA

TRYPANOSOMA-BRUCEI

ENDOPLASMIC-RETICULUM

PROTEIN

TRANSLOCATION

ALU-DOMAIN

GENE

IDENTIFICATION

PURIFICATION

PHYLOGENIES

SEQUENCES

CHAELI S

1992

MOLECULAR AND BIOCHEMICAL PARASITOLOGY

V51

P55

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