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The Arabidopsis thaliana CUTA gene encodes an evolutionarily conserved copper binding chloroplast protein
Author(s) -
Burkhead Jason L.,
AbdelGhany Salah E.,
Morrill Jonathan M.,
PilonSmits Elizabeth A. H.,
Pilon Marinus
Publication year - 2003
Publication title -
the plant journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.058
H-Index - 269
eISSN - 1365-313X
pISSN - 0960-7412
DOI - 10.1046/j.1365-313x.2003.01769.x
Subject(s) - biology , chloroplast , arabidopsis thaliana , transit peptide , peptide sequence , conserved sequence , intron , rna splicing , arabidopsis , microbiology and biotechnology , gene , biochemistry , rna , plastid , mutant
Summary The Arabidopsis thaliana CUTA gene encodes a 182‐amino‐acid‐long putative precursor of a chloroplast protein with high sequence similarity to evolutionarily conserved prokaryotic proteins implicated in copper tolerance. Northern analysis indicates that AtCUTA mRNA is expressed in all major tissue types. Analysis of cDNA clones and RT‐PCR with total mRNA revealed alternative splicing of AtCUTA by retention of an intron. The intron‐containing mRNA encodes a truncated 156‐amino‐acid protein as a result of stop codons in the included intron. The sequence of AtCutAp encoded by the fully spliced transcript suggests that the precursor consists of three domains: an N‐terminal chloroplast transit sequence of 70 residues, followed by a domain with prokaryotic signal‐sequence‐like characteristics and finally the most conserved C‐terminal domain. The N‐terminal chloroplast transit sequence was functional to route a passenger protein into isolated pea chloroplasts with possible sorting to the envelope. Chloroplast localization was confirmed by Western blot analysis of isolated and fractionated chloroplasts. Recombinant AtCutA protein was expressed in Escherichia coli without the N‐terminal 70‐amino‐acid chloroplast transit sequence. This recombinant AtCutAp was routed to the bacterial periplasm of E. coli . Purified recombinant AtCutAp is tetrameric and selectively binds Cu(II) ions with an affinity comparable to that reported for mammalian prion proteins.