Abstract

Major intrinsic proteins (MIPs) also called aquaporins form pores in membranes to facilitate the permeation of water and certain small polar solutes across membranes. MIPs are present in virtually every organism but are uniquely abundant in land plants. To elucidate the evolution and function of MIPs in terrestrial plants, the MIPs encoded in the genome of the spikemoss Selaginella moellendorffii were identified and analyzed. In total 19 MIPs were found in S. moellendorffii belonging to 6 of the 7 MIP subfamilies previously identified in the moss Physcomitrella patens. Only three of the MIPs were classified as members of the conserved water specific plasma membrane intrinsic protein (PIP) subfamily whereas almost half were found to belong to the diverse NOD26-like intrinsic protein (NIP) subfamily permeating various solutes. The small number of PIPs in S. moellendorffii is striking compared to all other land plants and no other species has more NIPs than PIPs. Similar to moss, S. moellendorffii only has one type of tonoplast intrinsic protein (TIP). Based on ESTs from non-angiosperms we conclude that the specialized groups of TIPs present in higher plants are not found in primitive vascular plants but evolved later in a common ancestor of seed plants. We also note that the silicic acid permeable NIP2 group that has been reported from angiosperms appears at the same time. We suggest that the expansion of the number MIP isoforms in higher plants is primarily associated with an increase in the different types of specialized tissues rather than the emergence of vascular tissue per se and that the loss of subfamilies has been possible due to a functional overlap between some subfamilies.

Highlights

  • The major intrinsic proteins (MIPs) constitute an ancient protein family and representatives can be found in virtually all types of organisms (Preston et al, 1992; Heymann and Engel, 1999)

  • MOELLENDORFFII MIPs The diploid genome of S. moellendorffii available at Joint Genome Institute was searched using the complete set of Physcomitrella patens MIPs as queries

  • Two sequences clustered with the tonoplast intrinsic protein (TIP) and eight with the NOD26-like intrinsic protein (NIP)

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Summary

Introduction

The major intrinsic proteins (MIPs) constitute an ancient protein family and representatives can be found in virtually all types of organisms (Preston et al, 1992; Heymann and Engel, 1999). Several structural features are conserved throughout the protein family such as the six transmembrane helices (H1–H6) connected by five loops (LA–LE) as well as two conserved NPA motifs (Asn-Pro-Ala) at the N-terminal end of two short helices in LB and LE (Fu et al, 2000; Sui et al, 2001). These oppositely oriented short helices connected by the two NPAmotifs facing each other in the middle of the membrane form a seventh helical transmembrane structure. Known as the aromatic/arginine-filter (ar/R filter), located toward the extracellular entrance form the narrowest part of the pore and are thought to determine the substrate selectivity (Fu et al, 2000; Beitz et al, 2006)

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