Complete nucleotide sequence of the chlorarachniophyte nucleomorph: Nature's smallest nucleus

被引:156
作者
Gilson, Paul R.
Su, Vanessa
Slamovits, Claudio H.
Reith, Michael E.
Keeling, Patrick J.
McFadden, Geoffrey I. [1 ]
机构
[1] Univ Melbourne, Sch Bot, Melbourne, Vic 3010, Australia
[2] Walter & Eliza Hall Inst Med Res, Infect & Immun Div, Parkville, Vic 3050, Australia
[3] CNR, Inst Marine Biosci, Halifax, NS B3H 3Z1, Canada
[4] Univ British Columbia, Dept Bot, Vancouver, BC V6T 1Z4, Canada
关键词
plastid; secondary endosymbiosis; intron; endosymbiosis;
D O I
10.1073/pnas.0600707103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The introduction of plastids into different heterotrophic protists created lineages of algae that diversified explosively, proliferated in marine and freshwater environments, and radically altered the biosphere. The origins of these secondary plastids are usually inferred from the presence of additional plastid membranes. However, two examples provide unique snapshots of secondary-endosymbiosis-in-action, because they retain a vestige of the endosymbiont nucleus known as the nucleomorph. These are chlorarachniophytes and cryptomonads, which acquired their plastids from a green and red alga respectively. To allow comparisons between them, we have sequenced the nucleomorph genome from the chlorarachniophyte Bigelowiella natans: at a mere 373,000 by and with only 331 genes, the smallest nuclear genome known and a model for extreme reduction. The genome is eukaryotic in nature, with three linear chromosomes containing densely packed genes with numerous overlaps. The genome is replete with 852 introns, but these are the smallest introns known, being only 18, 19, 20, or 21 nt in length. These pygmy introns are shown to be miniaturized versions of normal-sized introns present in the endosymbiont at the time of capture. Seventeen nucleomorph genes encode proteins that function in the plastid. The other nucleomorph genes are housekeeping entities, presumably underpinning maintenance and expression of these plastid proteins. Chlorarachniophyte plastids are thus serviced by three different genomes (plastid, nucleomorph, and host nucleus) requiring remarkable coordination and targeting. Although originating by two independent endosymbioses, chlorarachniophyte and cryptomonad nucleomorph genomes have converged upon remarkably similar architectures but differ in many molecular details that reflect two distinct trajectories to hypercompaction and reduction.
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页码:9566 / 9571
页数:6
相关论文
共 41 条
[1]   The function of genomes in bioenergetic organelles [J].
Allen, JF .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2003, 358 (1429) :19-37
[2]   Jumping genes and shrinking genomes - Probing the evolution of eukaryotic photosynthesis with genomics [J].
Archibald, JM .
IUBMB LIFE, 2005, 57 (08) :539-547
[3]   Lateral gene transfer and the evolution of plastid-targeted proteins in the secondary plastid-containing alga Bigelowiella natans [J].
Archibald, JM ;
Rogers, MB ;
Toop, M ;
Ishida, K ;
Keeling, PJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (13) :7678-7683
[4]   The genome of the diatom Thalassiosira pseudonana:: Ecology, evolution, and metabolism [J].
Armbrust, EV ;
Berges, JA ;
Bowler, C ;
Green, BR ;
Martinez, D ;
Putnam, NH ;
Zhou, SG ;
Allen, AE ;
Apt, KE ;
Bechner, M ;
Brzezinski, MA ;
Chaal, BK ;
Chiovitti, A ;
Davis, AK ;
Demarest, MS ;
Detter, JC ;
Glavina, T ;
Goodstein, D ;
Hadi, MZ ;
Hellsten, U ;
Hildebrand, M ;
Jenkins, BD ;
Jurka, J ;
Kapitonov, VV ;
Kröger, N ;
Lau, WWY ;
Lane, TW ;
Larimer, FW ;
Lippmeier, JC ;
Lucas, S ;
Medina, M ;
Montsant, A ;
Obornik, M ;
Parker, MS ;
Palenik, B ;
Pazour, GJ ;
Richardson, PM ;
Rynearson, TA ;
Saito, MA ;
Schwartz, DC ;
Thamatrakoln, K ;
Valentin, K ;
Vardi, A ;
Wilkerson, FP ;
Rokhsar, DS .
SCIENCE, 2004, 306 (5693) :79-86
[5]   Economy, speed and size matter: Evolutionary forces driving nuclear genome miniaturization and expansion [J].
Cavalier-Smith, T .
ANNALS OF BOTANY, 2005, 95 (01) :147-175
[6]   PROTOZOA AS HOSTS FOR ENDOSYMBIOSES AND THE CONVERSION OF SYMBIONTS INTO ORGANELLES [J].
CAVALIERSMITH, T ;
LEE, JJ .
JOURNAL OF PROTOZOOLOGY, 1985, 32 (03) :376-379
[7]   LIMITATIONS TO IN-VIVO IMPORT OF HYDROPHOBIC PROTEINS INTO YEAST MITOCHONDRIA - THE CASE OF A CYTOPLASMICALLY SYNTHESIZED APOCYTOCHROME-B [J].
CLAROS, MG ;
PEREA, J ;
SHU, YM ;
SAMATEY, FA ;
POPOT, JL ;
JACQ, C .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 228 (03) :762-771
[8]   Intracellular gene transfer:: Reduced hydrophobicity facilitates gene transfer for subunit 2 of cytochrome c oxidase [J].
Daley, DO ;
Clifton, R ;
Whelan, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (16) :10510-10515
[9]   Evidence for nucleomorph to host nucleus gene transfer: Light-harvesting complex proteins from cryptomonads and chlorarachniophytes [J].
Deane, JA ;
Fraunholz, M ;
Su, V ;
Maier, UG ;
Martin, W ;
Durnford, DG ;
McFadden, GI .
PROTIST, 2000, 151 (03) :239-252
[10]   Intron-exon structures of eukaryotic model organisms [J].
Deutsch, M ;
Long, M .
NUCLEIC ACIDS RESEARCH, 1999, 27 (15) :3219-3228