Literature DB >> 7337818

Eukaryote kingdoms: seven or nine?

T Cavalier-Smith.   

Abstract

The primary taxa of eukaryote classification should be monophyletic and based on fundamental cell structure rather than nutritional adaptive zones. The classical two kingdom classification into "plants" and "animals" and the newer four kingdom classifications into "protis", "fungi" "animals" and "plants" are therefore both unsatisfactory. Eukaryotes can be classified into nine kingdoms each defined in terms of a unique constellation of cell structures. Five kingdoms have plate-like mitochondrial cristae: (1) Eufungi (the non-ciliated fungi, which unlike the other eight kingdoms have unstacked Golgi cisternae), (2) Ciliofungi (the posteriorly ciliated fungi), (3) Animalia (Animals, sponges, mesozoa, and choanociliates; phagotrophs with basically posterior ciliation), (4) Biliphyta (Non-phagotrophic, phycobilisome-containing, algae; i.e. theGlaucophyceae and Rhodophyceae), (5) Viridiplantae (Non-phagotrophic green plants, with starch-containing plastids). Kingdom (6), the Euglenozoa, has disc-shaped cristae and an intraciliary dense rod and may be phagotrophic and/or phototrophic with plastids with three-membraned envelopes. Kingdom (7), the cryptophyta, has flattened tubular cristae, tubular mastigonemes on both cilia,m and starch in thecompartment between the plastid endoplasmic reticulum and the plastid envelope; their plastids, if present, have phycobilins inside the paired thylakoids and chlorophyll c2. Kingdom (8), the Chromophyta, has tubular cristae, together with tubular mastigonemes on one anterior cilum and/or a plastid endoplasmic reticulum and chlorophyll c1 + c2. Members of the ninth kingdom, the Protozoa, are mainly phagotrophic, and have tubular or vesicular cristae (or lack mitochondria altogether), and lack tubular mastigonemes on their (primitively anterior) cilia; plastids if present have three-envelop membranes, chlorophyll c2, and no internal starch, and a plastid endoplasmic reticulum is absent. Kingdoms 4-9 are primitively anteriorly biciliate. Detailed definitions of the new kingdoms and lists of the phyla comprising them are given. Advantages of the new system and its main phylogenetic implications are discussed. A simpler system of five kingdoms suitable for very elementary teaching is possible by grouping the photosynthetic and fungal kindoms in pairs. Various compromises are possible between the nine and five kingdoms systems; it is suggested that the best one for general scientific use is a system of seven kingdoms in which the Eufungi and Ciliofungi become subkingdoms of the Kingdom Fungi, and the Cryptophyta andChromophyta subkingdoms of th Kingdom Chromista; the Fungi, Viridiplantae, Biliphyta, and Chromista can be subject to the Botanical Code of Nomenclature, while the Zoological Code can govern the Kingdoms Animalia, Protozoa and Euglenozoa...

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Year:  1981        PMID: 7337818     DOI: 10.1016/0303-2647(81)90050-2

Source DB:  PubMed          Journal:  Biosystems        ISSN: 0303-2647            Impact factor:   1.973


  51 in total

1.  The tmRNA website: reductive evolution of tmRNA in plastids and other endosymbionts.

Authors:  Pulcherie Gueneau de Novoa; Kelly P Williams
Journal:  Nucleic Acids Res       Date:  2004-01-01       Impact factor: 16.971

2.  Broadly sampled multigene analyses yield a well-resolved eukaryotic tree of life.

Authors:  Laura Wegener Parfrey; Jessica Grant; Yonas I Tekle; Erica Lasek-Nesselquist; Hilary G Morrison; Mitchell L Sogin; David J Patterson; Laura A Katz
Journal:  Syst Biol       Date:  2010-07-23       Impact factor: 15.683

Review 3.  After the primary endosymbiosis: an update on the chromalveolate hypothesis and the origins of algae with Chl c.

Authors:  Beverley R Green
Journal:  Photosynth Res       Date:  2010-07-30       Impact factor: 3.573

4.  Photoreceptor for curling behavior in Peranema trichophorum and evolution of eukaryotic rhodopsins.

Authors:  Jureepan Saranak; Kenneth W Foster
Journal:  Eukaryot Cell       Date:  2005-10

5.  Substitutional bias confounds inference of cyanelle origins from sequence data.

Authors:  P J Lockhart; C J Howe; D A Bryant; T J Beanland; A W Larkum
Journal:  J Mol Evol       Date:  1992-02       Impact factor: 2.395

6.  Unique mitochondrial genome structure in diplonemids, the sister group of kinetoplastids.

Authors:  William Marande; Julius Lukes; Gertraud Burger
Journal:  Eukaryot Cell       Date:  2005-06

Review 7.  Protein targeting into plastids: a key to understanding the symbiogenetic acquisitions of plastids.

Authors:  Ken-ichiro Ishida
Journal:  J Plant Res       Date:  2005-07-26       Impact factor: 2.629

8.  Evidence for multiple xenogenous origins of plastids: comparison of psbA-genes with a xanthophyte sequence.

Authors:  S Scherer; G Herrmann; J Hirschberg; P Böger
Journal:  Curr Genet       Date:  1991-06       Impact factor: 3.886

9.  Eukaryotic origins: string analysis of 5S ribosomal RNA sequences from some relevant organisms.

Authors:  D L Nanney; D O Mobley; R M Preparata; E B Meyer; E M Simon
Journal:  J Mol Evol       Date:  1991-04       Impact factor: 2.395

10.  psbD sequences of Bumilleriopsis filiformis (Heterokontophyta, Xanthophyceae) and Porphyridium purpureum (Rhodophyta, Bangiophycidae): evidence for polyphyletic origins of plastids.

Authors:  S Scherer; S Lechner; P Böger
Journal:  Curr Genet       Date:  1993-11       Impact factor: 3.886

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