RNA-Dependent Cysteine Biosynthesis in Archaea

Author:

Sauerwald Anselm12345,Zhu Wenhong12345,Major Tiffany A.12345,Roy Hervé12345,Palioura Sotiria12345,Jahn Dieter12345,Whitman William B.12345,Yates John R.12345,Ibba Michael12345,Söll Dieter12345

Affiliation:

1. Department of Molecular Biophysics and Biochemistry

2. Department of Chemistry, Yale University, New Haven, CT 06520–8114, USA.

3. Department of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.

4. Department of Microbiology, University of Georgia, Athens, GA 30602–2605, USA.

5. Department of Microbiology, The Ohio State University, Columbus, OH 43210–1292, USA.

Abstract

Several methanogenic archaea lack cysteinyl–transfer RNA (tRNA) synthetase (CysRS), the essential enzyme that provides Cys-tRNA Cys for translation in most organisms. Partial purification of the corresponding activity from Methanocaldococcus jannaschii indicated that tRNA Cys becomes acylated with O -phosphoserine (Sep) but not with cysteine. Further analyses identified a class II–type O -phosphoseryl-tRNA synthetase (SepRS) and Sep-tRNA:Cys-tRNA synthase (SepCysS). SepRS specifically forms Sep-tRNA Cys , which is then converted to Cys-tRNA Cys by SepCysS. Comparative genomic analyses suggest that this pathway, encoded in all organisms lacking CysRS, can also act as the sole route for cysteine biosynthesis. This was proven for Methanococcus maripaludis , where deletion of the SepRS-encoding gene resulted in cysteine auxotrophy. As the conversions of Sep-tRNA to Cys-tRNA or to selenocysteinyl-tRNA are chemically analogous, the catalytic activity of SepCysS provides a means by which both cysteine and selenocysteine may have originally been added to the genetic code.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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