The endosymbiotic origin of the protein import machinery of chloroplastic envelope membranes

被引:92
作者
Reumann, S [1 ]
Keegstra, K [1 ]
机构
[1] Michigan State Univ, Dept Energy, Plant Res Lab, E Lansing, MI 48824 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/S1360-1385(99)01449-1
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Chloroplasts have evolved a complex proteinaceous machinery to import nuclear-encoded proteins. The origin of this machinery, following the endosymbiotic events leading to chloroplasts, is an intriguing, unresolved problem. Given that cyanobacteria are the probable ancestors of chloroplasts, the genome sequence of Synechocystis sp. PCC 6803 offers a valuable resource to identify putative homologs for components of this protein import machinery and to gain insights into its possibly endosymbiotic origin. Detailed computational sequence analysis reveals that Synechocystis sp, PCC 6803 has homologs of three of the known membrane proteins of the chloroplastic translocon, namely Toc75, Tic20 and Tic22, as well as a homolog of the putative component Tic55. Thus, the chloroplastic protein import machinery is mainly derived from the endosymbiotic cyanobacterium, but, interestingly, not from any of the four main protein secretion systems of prokaryotes. The relatively high sequence variability between chloroplastic and Synechocystis proteins suggests that the ancestral proteins had different physiological roles and were modified significantly to fulfill the new demand of importing proteins into the evolving chloroplast, The fact that some chloroplastic protein import components are not related to any Synechocystis proteins (Toc159, Tic110 and Toc34) indicates that the chloroplastic protein import apparatus is of a dual evolutionary origin.
引用
收藏
页码:302 / 307
页数:6
相关论文
共 27 条
[1]   Identification of protein transport complexes in the chloroplastic envelope membranes via chemical cross-linking [J].
Akita, M ;
Nielsen, E ;
Keegstra, K .
JOURNAL OF CELL BIOLOGY, 1997, 136 (05) :983-994
[2]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[3]   A protein import receptor in pea chloroplasts, Toc86, is only a proteolytic fragment of a larger polypeptide [J].
Bölter, B ;
May, T ;
Soll, J .
FEBS LETTERS, 1998, 441 (01) :59-62
[4]   Origin of a chloroplast protein importer [J].
Bölter, B ;
Soll, J ;
Schulz, A ;
Hinnah, S ;
Wagner, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (26) :15831-15836
[5]   The chloroplastic protein import machinery contains a Rieske-type iron-sulfur cluster and a mononuclear iron-binding protein [J].
Caliebe, A ;
Grimm, R ;
Kaiser, G ;
Lübeck, J ;
Soll, J ;
Heins, L .
EMBO JOURNAL, 1997, 16 (24) :7342-7350
[6]   The protein translocation apparatus of chloroplast envelopes [J].
Heins, L ;
Collinson, I ;
Soll, J .
TRENDS IN PLANT SCIENCE, 1998, 3 (02) :56-61
[7]   Reconstitution of a chloroplast protein import channel [J].
Hinnah, SC ;
Hill, K ;
Wagner, R ;
Schlicher, T ;
Soll, J .
EMBO JOURNAL, 1997, 16 (24) :7351-7360
[8]   A RECEPTOR COMPONENT OF THE CHLOROPLAST PROTEIN TRANSLOCATION MACHINERY [J].
HIRSCH, S ;
MUCKEL, E ;
HEEMEYER, F ;
VONHEIJNE, G ;
SOLL, J .
SCIENCE, 1994, 266 (5193) :1989-1992
[9]  
Kaneko T, 1996, DNA Res, V3, P109
[10]   Protein import and routing systems of chloroplasts [J].
Keegstra, K ;
Cline, K .
PLANT CELL, 1999, 11 (04) :557-570