Phylogenetic context and basal metazoan model systems

被引:37
作者
Collins, AG
Cartwright, P
McFadden, CS
Schierwater, B
机构
[1] ITZ, D-30559 Hannover, Germany
[2] Univ Kansas, Dept Ecol & Evolutionary Biol, Lawrence, KS 66045 USA
[3] Harvey Mudd Coll, Dept Biol, Claremont, CA 91711 USA
关键词
D O I
10.1093/icb/45.4.585
中图分类号
Q95 [动物学];
学科分类号
071002 ;
摘要
In comparative studies using model organisms, extant taxa are often referred to as basal. The term suggests that such taxa are descendants of lineages that diverged early in the history of some larger taxon. By this usage, the basal metazoans comprise just four phyla (Placozoa, Porifera, Cnidaria, and Cten-ophora) and the large clade Bilateria. We advise against this practice because basal refers to a region at the base or root of a phylogenetic tree. Thus, referring to an extant taxon or species as basal, or as more basal than another, can be misleading. While much progress has been made toward understanding some of the phylogenetic relationships within these groups, the relationships among them are still largely not known with certainty. Thus, sound inferences from comparative studies of model organisms demand continued illumination of phylogeny. Hypotheses about the mechanisms underlying metazoan evolution can be drawn from the study of model organisms in Cnidaria, Ctenophora, Placozoa, and Porifera, but it is clear that these model organisms are likely to be derived in many respects. Therefore, testing these hypotheses requires the study of yet additional model organisms. The most effective tests are those that investigate model organisms with phylogenetic positions among two sister groups comprising a larger clade of interest.
引用
收藏
页码:585 / 594
页数:10
相关论文
共 121 条
[41]  
Haeckl E., 1874, Q J Microscop Sci, P142, DOI DOI 10.1242/JCS.S2-14.54.142
[42]  
HARBISON GR, 1985, ORIGINS RELATIONSHIP
[43]   The level of expression of a protein kinase C gene may be an important component of the patterning process in Hydra [J].
Hassel, M ;
Bridge, DM ;
Stover, NA ;
Kleinholz, H ;
Steele, RE .
DEVELOPMENT GENES AND EVOLUTION, 1998, 207 (08) :502-514
[44]   Localized expression of a dpp/BMP2/4 ortholog in a coral embryo [J].
Hayward, DC ;
Samuel, G ;
Pontynen, PC ;
Catmull, J ;
Saint, R ;
Miller, DJ ;
Ball, EE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (12) :8106-8111
[45]  
Hayward DC, 2001, DEV GENES EVOL, V211, P10
[46]  
HAYWARD DC, 2004, DEV GENES EVOL
[47]   WNT signalling molecules act in axis formation in the diploblastic metazoan Hydra [J].
Hobmayer, B ;
Rentzsch, F ;
Kuhn, K ;
Happel, CM ;
von Laue, CC ;
Snyder, P ;
Rothbächer, U ;
Holstein, TW .
NATURE, 2000, 407 (6801) :186-189
[48]  
Hyman L. H., 1940, PROTOZOA CTENOPHORA
[49]   The Trox-2 Hox/ParaHox gene of Trichoplax (Placozoa) marks an epithelial boundary [J].
Jakob, W ;
Sagasser, S ;
Dellaporta, S ;
Holland, P ;
Kuhn, K ;
Schierwater, B .
DEVELOPMENT GENES AND EVOLUTION, 2004, 214 (04) :170-175
[50]   MODEL ORGANISMS IN EVOLUTIONARY STUDIES [J].
KELLOGG, EA ;
SHAFFER, HB .
SYSTEMATIC BIOLOGY, 1993, 42 (04) :409-414