Secreted and plasma membrane proteins play crucial roles in a variety of ph
ysiological and developmental processes of multicellular organisms. Systema
tic cloning of the genes encoding these proteins is therefore of general in
terest. An effective method of trapping signal sequences was first describe
d by Tashiro et al. (1993), and a similar yet more efficient method was rep
orted by Klein et al. (1996) and Jacobs et al. (1997). In this study, we ca
rried out the latter yeast-based signal sequence trap to clone genes from A
rabidopsis thaliana encoding secreted and plasma membrane proteins. Of 144
sequenced cDNA clones, 18% are identical to previously cloned Arabidopsis t
haliana genes, 12% are homologous to genes identified from various organism
s, and 46% are novel. All of the isolated genes identical or homologous to
previously reported genes are either secreted or plasma membrane proteins,
and the remaining novel genes appear to contain functional signal sequences
based on computer-aided sequence analysis. The full-length cDNA clones of
one homologous gene and another novel gene were isolated and sequenced. The
deduced amino acid sequences suggest that the former encodes a secreted pr
otein, and the latter encodes a type 1 membrane protein. These results indi
cate that the signal sequence trap method is effective and useful for the i
solation of plant genes encoding secreted and plasma membrane proteins.