Expression profiles of urbilaterian genes uniquely shared between honey bee and vertebrates

Background Large-scale comparison of metazoan genomes has revealed that a significant fraction of genes of the last common ancestor of Bilateria (Urbilateria) is lost in each animal lineage. This event could be one of the underlying mechanisms involved in generating metazoan diversity. However, the...

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Veröffentlicht in:BMC Genomics Jg. 10; H. 1; S. 17
Hauptverfasser: Matsui, Toshiaki, Yamamoto, Toshiyuki, Wyder, Stefan, Zdobnov, Evgeny M, Kadowaki, Tatsuhiko
Format: Journal Article
Sprache:Englisch
Veröffentlicht: London Springer Science and Business Media LLC 12.01.2009
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ISSN:1471-2164, 1471-2164
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Abstract Background Large-scale comparison of metazoan genomes has revealed that a significant fraction of genes of the last common ancestor of Bilateria (Urbilateria) is lost in each animal lineage. This event could be one of the underlying mechanisms involved in generating metazoan diversity. However, the present functions of these ancient genes have not been addressed extensively. To understand the functions and evolutionary mechanisms of such ancient Urbilaterian genes, we carried out comprehensive expression profile analysis of genes shared between vertebrates and honey bees but not with the other sequenced ecdysozoan genomes (honey bee-vertebrate specific, HVS genes) as a model. Results We identified 30 honey bee and 55 mouse HVS genes. Many HVS genes exhibited tissue-selective expression patterns; intriguingly, the expression of 60% of honey bee HVS genes was found to be brain enriched, and 24% of mouse HVS genes were highly expressed in either or both the brain and testis. Moreover, a minimum of 38% of mouse HVS genes demonstrated neuron-enriched expression patterns, and 62% of them exhibited expression in selective brain areas, particularly the forebrain and cerebellum. Furthermore, gene ontology (GO) analysis of HVS genes predicted that 35% of genes are associated with DNA transcription and RNA processing. Conclusion These results suggest that HVS genes include genes that are biased towards expression in the brain and gonads. They also demonstrate that at least some of Urbilaterian genes retained in the specific animal lineage may be selectively maintained to support the species-specific phenotypes.
AbstractList Large-scale comparison of metazoan genomes has revealed that a significant fraction of genes of the last common ancestor of Bilateria (Urbilateria) is lost in each animal lineage. This event could be one of the underlying mechanisms involved in generating metazoan diversity. However, the present functions of these ancient genes have not been addressed extensively. To understand the functions and evolutionary mechanisms of such ancient Urbilaterian genes, we carried out comprehensive expression profile analysis of genes shared between vertebrates and honey bees but not with the other sequenced ecdysozoan genomes (honey bee-vertebrate specific, HVS genes) as a model. We identified 30 honey bee and 55 mouse HVS genes. Many HVS genes exhibited tissue-selective expression patterns; intriguingly, the expression of 60% of honey bee HVS genes was found to be brain enriched, and 24% of mouse HVS genes were highly expressed in either or both the brain and testis. Moreover, a minimum of 38% of mouse HVS genes demonstrated neuron-enriched expression patterns, and 62% of them exhibited expression in selective brain areas, particularly the forebrain and cerebellum. Furthermore, gene ontology (GO) analysis of HVS genes predicted that 35% of genes are associated with DNA transcription and RNA processing. These results suggest that HVS genes include genes that are biased towards expression in the brain and gonads. They also demonstrate that at least some of Urbilaterian genes retained in the specific animal lineage may be selectively maintained to support the species-specific phenotypes.
Abstract Background Large-scale comparison of metazoan genomes has revealed that a significant fraction of genes of the last common ancestor of Bilateria (Urbilateria) is lost in each animal lineage. This event could be one of the underlying mechanisms involved in generating metazoan diversity. However, the present functions of these ancient genes have not been addressed extensively. To understand the functions and evolutionary mechanisms of such ancient Urbilaterian genes, we carried out comprehensive expression profile analysis of genes shared between vertebrates and honey bees but not with the other sequenced ecdysozoan genomes (honey bee-vertebrate specific, HVS genes) as a model. Results We identified 30 honey bee and 55 mouse HVS genes. Many HVS genes exhibited tissue-selective expression patterns; intriguingly, the expression of 60% of honey bee HVS genes was found to be brain enriched, and 24% of mouse HVS genes were highly expressed in either or both the brain and testis. Moreover, a minimum of 38% of mouse HVS genes demonstrated neuron-enriched expression patterns, and 62% of them exhibited expression in selective brain areas, particularly the forebrain and cerebellum. Furthermore, gene ontology (GO) analysis of HVS genes predicted that 35% of genes are associated with DNA transcription and RNA processing. Conclusion These results suggest that HVS genes include genes that are biased towards expression in the brain and gonads. They also demonstrate that at least some of Urbilaterian genes retained in the specific animal lineage may be selectively maintained to support the species-specific phenotypes.
Large-scale comparison of metazoan genomes has revealed that a significant fraction of genes of the last common ancestor of Bilateria (Urbilateria) is lost in each animal lineage. This event could be one of the underlying mechanisms involved in generating metazoan diversity. However, the present functions of these ancient genes have not been addressed extensively. To understand the functions and evolutionary mechanisms of such ancient Urbilaterian genes, we carried out comprehensive expression profile analysis of genes shared between vertebrates and honey bees but not with the other sequenced ecdysozoan genomes (honey bee-vertebrate specific, HVS genes) as a model.BACKGROUNDLarge-scale comparison of metazoan genomes has revealed that a significant fraction of genes of the last common ancestor of Bilateria (Urbilateria) is lost in each animal lineage. This event could be one of the underlying mechanisms involved in generating metazoan diversity. However, the present functions of these ancient genes have not been addressed extensively. To understand the functions and evolutionary mechanisms of such ancient Urbilaterian genes, we carried out comprehensive expression profile analysis of genes shared between vertebrates and honey bees but not with the other sequenced ecdysozoan genomes (honey bee-vertebrate specific, HVS genes) as a model.We identified 30 honey bee and 55 mouse HVS genes. Many HVS genes exhibited tissue-selective expression patterns; intriguingly, the expression of 60% of honey bee HVS genes was found to be brain enriched, and 24% of mouse HVS genes were highly expressed in either or both the brain and testis. Moreover, a minimum of 38% of mouse HVS genes demonstrated neuron-enriched expression patterns, and 62% of them exhibited expression in selective brain areas, particularly the forebrain and cerebellum. Furthermore, gene ontology (GO) analysis of HVS genes predicted that 35% of genes are associated with DNA transcription and RNA processing.RESULTSWe identified 30 honey bee and 55 mouse HVS genes. Many HVS genes exhibited tissue-selective expression patterns; intriguingly, the expression of 60% of honey bee HVS genes was found to be brain enriched, and 24% of mouse HVS genes were highly expressed in either or both the brain and testis. Moreover, a minimum of 38% of mouse HVS genes demonstrated neuron-enriched expression patterns, and 62% of them exhibited expression in selective brain areas, particularly the forebrain and cerebellum. Furthermore, gene ontology (GO) analysis of HVS genes predicted that 35% of genes are associated with DNA transcription and RNA processing.These results suggest that HVS genes include genes that are biased towards expression in the brain and gonads. They also demonstrate that at least some of Urbilaterian genes retained in the specific animal lineage may be selectively maintained to support the species-specific phenotypes.CONCLUSIONThese results suggest that HVS genes include genes that are biased towards expression in the brain and gonads. They also demonstrate that at least some of Urbilaterian genes retained in the specific animal lineage may be selectively maintained to support the species-specific phenotypes.
Background Large-scale comparison of metazoan genomes has revealed that a significant fraction of genes of the last common ancestor of Bilateria (Urbilateria) is lost in each animal lineage. This event could be one of the underlying mechanisms involved in generating metazoan diversity. However, the present functions of these ancient genes have not been addressed extensively. To understand the functions and evolutionary mechanisms of such ancient Urbilaterian genes, we carried out comprehensive expression profile analysis of genes shared between vertebrates and honey bees but not with the other sequenced ecdysozoan genomes (honey bee-vertebrate specific, HVS genes) as a model. Results We identified 30 honey bee and 55 mouse HVS genes. Many HVS genes exhibited tissue-selective expression patterns; intriguingly, the expression of 60% of honey bee HVS genes was found to be brain enriched, and 24% of mouse HVS genes were highly expressed in either or both the brain and testis. Moreover, a minimum of 38% of mouse HVS genes demonstrated neuron-enriched expression patterns, and 62% of them exhibited expression in selective brain areas, particularly the forebrain and cerebellum. Furthermore, gene ontology (GO) analysis of HVS genes predicted that 35% of genes are associated with DNA transcription and RNA processing. Conclusion These results suggest that HVS genes include genes that are biased towards expression in the brain and gonads. They also demonstrate that at least some of Urbilaterian genes retained in the specific animal lineage may be selectively maintained to support the species-specific phenotypes.
ArticleNumber 17
Audience Academic
Author Toshiaki Matsui
Tatsuhiko Kadowaki
Stefan Wyder
Toshiyuki Yamamoto
Evgeny M. Zdobnov
AuthorAffiliation 3 Swiss Institute of Bioinformatics, 1 rue Michel-Servet, 1211 Geneva, Switzerland
1 Department of Applied Biological Sciences, School of Agricultural Sciences, Nagoya University, Chikusa, Nagoya 464-8601, Japan
2 Department of Genetic Medicine and Development, University of Geneva Medical School, 1 rue Michel-Servet, 1211 Geneva, Switzerland
4 Imperial College London, South Kensington Campus, SW7 2AZ, London, UK
5 Graduate School of Bioagricultural Sciences, Nagoya University, Chikusa, Nagoya 464-8601, Japan
AuthorAffiliation_xml – name: 5 Graduate School of Bioagricultural Sciences, Nagoya University, Chikusa, Nagoya 464-8601, Japan
– name: 3 Swiss Institute of Bioinformatics, 1 rue Michel-Servet, 1211 Geneva, Switzerland
– name: 4 Imperial College London, South Kensington Campus, SW7 2AZ, London, UK
– name: 1 Department of Applied Biological Sciences, School of Agricultural Sciences, Nagoya University, Chikusa, Nagoya 464-8601, Japan
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Cites_doi 10.1016/j.ydbio.2005.04.033
10.1016/S0092-8674(02)00932-7
10.1038/nature06784
10.1038/nature05260
10.1242/dev.00716
10.1126/science.1135213
10.1016/j.cell.2006.09.052
10.1016/j.cell.2008.01.003
10.1152/physiolgenomics.00040.2001
10.1016/S0092-8674(02)00933-9
10.1074/jbc.M205183200
10.1186/gb-2007-8-11-r242
10.1016/S1364-6613(00)01601-6
10.1016/j.tig.2005.09.007
10.1016/j.tig.2005.08.002
10.1101/gr.8.6.590
10.1186/gb-2006-7-5-r43
10.1126/science.1077061
10.1126/science.1080049
10.1111/j.1525-142X.2005.05022.x
10.1016/j.cub.2003.11.030
10.1146/annurev.ne.19.030196.002115
10.1126/science.1138878
10.1126/science.1102210
10.1186/1471-2148-6-5
10.1371/journal.pbio.0030314
10.1074/jbc.M308104200
10.1182/blood.V80.4.879.879
10.1126/science.1119089
10.1101/lm.2.5.199
10.1038/nature06341
10.1093/molbev/msh010
10.1101/gr.771603
10.1038/nature03158
10.1016/S1359-6101(03)00032-7
10.1126/science.1076181
10.1128/MCB.23.2.474-481.2003
10.1016/S0092-8674(00)81656-6
10.1038/nature05453
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Issue 1
Keywords Tumor Necrosis Factor Receptor Superfamily
Gene Network Interaction
TBLASTN Analysis
Metazoan Genome
Gene Ontology
Language English
License This is an Open Access article distributed under the terms of the Creative Commons Attribution License (), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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References EM Zdobnov (1901_CR39) 2002; 298
Tribolium genome sequencing consortium (1901_CR16) 2008; 452
AR Mushegian (1901_CR29) 1998; 8
N Kunert (1901_CR37) 2003; 130
LL Moroz (1901_CR5) 2006; 127
L Zhang (1901_CR32) 2004; 21
M Okano (1901_CR25) 1999; 99
P Dehal (1901_CR30) 2002; 298
CH Shin (1901_CR21) 2002; 110
U Technau (1901_CR3) 2005; 21
DJ Miller (1901_CR4) 2005; 21
Y Wang (1901_CR18) 2006; 314
R Menzel (1901_CR10) 2001; 5
A Beigneux (1901_CR23) 2002; 277
EM De Robertis (1901_CR7) 2008; 132
P Dehal (1901_CR33) 2005; 3
CF Ware (1901_CR34) 2003; 14
R Menzel (1901_CR9) 1996; 19
ES Lein (1901_CR28) 2007; 445
F Raible (1901_CR6) 2005; 310
RA Holt (1901_CR12) 2002; 298
The honeybee genome sequencing consortium (1901_CR15) 2006; 443
Biology analysis group (1901_CR14) 2004; 306
S Wyder (1901_CR17) 2007; 8
SJ Korsmeyer (1901_CR24) 1992; 80
T Blomme (1901_CR35) 2006; 7
RD Kortschak (1901_CR1) 2003; 13
S Muhlfriedel (1901_CR19) 2005; 283
A Kusserow (1901_CR2) 2005; 433
MA Salazar (1901_CR22) 2003; 278
F Chen (1901_CR20) 2002; 110
S Tateishi (1901_CR26) 2003; 23
SE Fahrbach (1901_CR8) 1995; 2
EGJ Danchin (1901_CR36) 2006; 6
H Mi (1901_CR27) 2003; 13
LL Hsiao (1901_CR38) 2001; 7
Drosophila 12 Genomes Consortium (1901_CR11) 2007; 450
V Nene (1901_CR13) 2007; 316
AL Hughes (1901_CR31) 2005; 7
12944428 - Development. 2003 Nov;130(21):5083-90
11166636 - Trends Cogn Sci. 2001 Feb 1;5(2):62-71
16128622 - PLoS Biol. 2005 Oct;3(10):e314
15967424 - Dev Biol. 2005 Jul 15;283(2):522-34
12151402 - J Biol Chem. 2002 Oct 11;277(41):38358-63
16098631 - Trends Genet. 2005 Oct;21(10):536-9
12509447 - Mol Cell Biol. 2003 Jan;23(2):474-81
12364791 - Science. 2002 Oct 4;298(5591):129-49
16311335 - Science. 2005 Nov 25;310(5752):1325-6
15591204 - Science. 2004 Dec 10;306(5703):1937-40
12364792 - Science. 2002 Oct 4;298(5591):149-59
18243095 - Cell. 2008 Jan 25;132(2):185-95
17190607 - Cell. 2006 Dec 29;127(7):1453-67
17510324 - Science. 2007 Jun 22;316(5832):1718-23
12481130 - Science. 2002 Dec 13;298(5601):2157-67
11773596 - Physiol Genomics. 2001 Dec 21;7(2):97-104
12297045 - Cell. 2002 Sep 20;110(6):713-23
1498330 - Blood. 1992 Aug 15;80(4):879-86
17151600 - Nature. 2007 Jan 11;445(7124):168-76
18362917 - Nature. 2008 Apr 24;452(7190):949-55
14680636 - Curr Biol. 2003 Dec 16;13(24):2190-5
12297046 - Cell. 2002 Sep 20;110(6):725-35
16420703 - BMC Evol Biol. 2006;6:5
10555141 - Cell. 1999 Oct 29;99(3):247-57
15650739 - Nature. 2005 Jan 13;433(7022):156-60
12952880 - Genome Res. 2003 Sep;13(9):2118-28
16226338 - Trends Genet. 2005 Dec;21(12):633-9
15876192 - Evol Dev. 2005 May-Jun;7(3):196-200
12787557 - Cytokine Growth Factor Rev. 2003 Jun-Aug;14(3-4):181-4
14506234 - J Biol Chem. 2003 Dec 5;278(49):49031-43
17073008 - Nature. 2006 Oct 26;443(7114):931-49
18021399 - Genome Biol. 2007;8(11):R242
17994087 - Nature. 2007 Nov 8;450(7167):203-18
10467576 - Learn Mem. 1995 Sep-Oct;2(5):199-224
14595094 - Mol Biol Evol. 2004 Feb;21(2):236-9
17068262 - Science. 2006 Oct 27;314(5799):645-7
8833448 - Annu Rev Neurosci. 1996;19:379-404
16723033 - Genome Biol. 2006;7(5):R43
9647634 - Genome Res. 1998 Jun;8(6):590-8
References_xml – volume: 283
  start-page: 522
  year: 2005
  ident: 1901_CR19
  publication-title: Dev Biol
  doi: 10.1016/j.ydbio.2005.04.033
– volume: 110
  start-page: 713
  year: 2002
  ident: 1901_CR20
  publication-title: Cell
  doi: 10.1016/S0092-8674(02)00932-7
– volume: 452
  start-page: 949
  year: 2008
  ident: 1901_CR16
  publication-title: Nature
  doi: 10.1038/nature06784
– volume: 443
  start-page: 931
  year: 2006
  ident: 1901_CR15
  publication-title: Nature
  doi: 10.1038/nature05260
– volume: 130
  start-page: 5083
  year: 2003
  ident: 1901_CR37
  publication-title: Development
  doi: 10.1242/dev.00716
– volume: 314
  start-page: 645
  year: 2006
  ident: 1901_CR18
  publication-title: Science
  doi: 10.1126/science.1135213
– volume: 127
  start-page: 1453
  year: 2006
  ident: 1901_CR5
  publication-title: Cell
  doi: 10.1016/j.cell.2006.09.052
– volume: 132
  start-page: 185
  year: 2008
  ident: 1901_CR7
  publication-title: Cell
  doi: 10.1016/j.cell.2008.01.003
– volume: 7
  start-page: 97
  year: 2001
  ident: 1901_CR38
  publication-title: Physiol Genomics
  doi: 10.1152/physiolgenomics.00040.2001
– volume: 110
  start-page: 725
  year: 2002
  ident: 1901_CR21
  publication-title: Cell
  doi: 10.1016/S0092-8674(02)00933-9
– volume: 277
  start-page: 38358
  year: 2002
  ident: 1901_CR23
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M205183200
– volume: 8
  start-page: R242
  year: 2007
  ident: 1901_CR17
  publication-title: Genome Biology
  doi: 10.1186/gb-2007-8-11-r242
– volume: 5
  start-page: 62
  year: 2001
  ident: 1901_CR10
  publication-title: Trends Cogn Sci
  doi: 10.1016/S1364-6613(00)01601-6
– volume: 21
  start-page: 633
  year: 2005
  ident: 1901_CR3
  publication-title: Trends Genet
  doi: 10.1016/j.tig.2005.09.007
– volume: 21
  start-page: 536
  year: 2005
  ident: 1901_CR4
  publication-title: Trends Genet
  doi: 10.1016/j.tig.2005.08.002
– volume: 8
  start-page: 590
  year: 1998
  ident: 1901_CR29
  publication-title: Genome Res
  doi: 10.1101/gr.8.6.590
– volume: 7
  start-page: R43
  year: 2006
  ident: 1901_CR35
  publication-title: Genome Biol
  doi: 10.1186/gb-2006-7-5-r43
– volume: 298
  start-page: 149
  year: 2002
  ident: 1901_CR39
  publication-title: Science
  doi: 10.1126/science.1077061
– volume: 298
  start-page: 2157
  year: 2002
  ident: 1901_CR30
  publication-title: Science
  doi: 10.1126/science.1080049
– volume: 7
  start-page: 196
  year: 2005
  ident: 1901_CR31
  publication-title: Evol & Dev
  doi: 10.1111/j.1525-142X.2005.05022.x
– volume: 13
  start-page: 2190
  year: 2003
  ident: 1901_CR1
  publication-title: Current Biol
  doi: 10.1016/j.cub.2003.11.030
– volume: 19
  start-page: 379
  year: 1996
  ident: 1901_CR9
  publication-title: Annu Rev Neurosci
  doi: 10.1146/annurev.ne.19.030196.002115
– volume: 316
  start-page: 1718
  year: 2007
  ident: 1901_CR13
  publication-title: Science
  doi: 10.1126/science.1138878
– volume: 306
  start-page: 1937
  year: 2004
  ident: 1901_CR14
  publication-title: Science
  doi: 10.1126/science.1102210
– volume: 6
  start-page: 5
  year: 2006
  ident: 1901_CR36
  publication-title: BMC Evol Biol
  doi: 10.1186/1471-2148-6-5
– volume: 3
  start-page: e314
  year: 2005
  ident: 1901_CR33
  publication-title: PLoS Biol
  doi: 10.1371/journal.pbio.0030314
– volume: 278
  start-page: 49031
  year: 2003
  ident: 1901_CR22
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M308104200
– volume: 80
  start-page: 879
  year: 1992
  ident: 1901_CR24
  publication-title: Blood
  doi: 10.1182/blood.V80.4.879.879
– volume: 310
  start-page: 1325
  year: 2005
  ident: 1901_CR6
  publication-title: Science
  doi: 10.1126/science.1119089
– volume: 2
  start-page: 199
  year: 1995
  ident: 1901_CR8
  publication-title: Learn & Mem
  doi: 10.1101/lm.2.5.199
– volume: 450
  start-page: 203
  year: 2007
  ident: 1901_CR11
  publication-title: Nature
  doi: 10.1038/nature06341
– volume: 21
  start-page: 236
  year: 2004
  ident: 1901_CR32
  publication-title: Mol Biol Evol
  doi: 10.1093/molbev/msh010
– volume: 13
  start-page: 2118
  year: 2003
  ident: 1901_CR27
  publication-title: Genome Res
  doi: 10.1101/gr.771603
– volume: 433
  start-page: 156
  year: 2005
  ident: 1901_CR2
  publication-title: Nature
  doi: 10.1038/nature03158
– volume: 14
  start-page: 181
  year: 2003
  ident: 1901_CR34
  publication-title: Cytokine Growth Factor Rev
  doi: 10.1016/S1359-6101(03)00032-7
– volume: 298
  start-page: 129
  year: 2002
  ident: 1901_CR12
  publication-title: Science
  doi: 10.1126/science.1076181
– volume: 23
  start-page: 474
  year: 2003
  ident: 1901_CR26
  publication-title: Mol Cell Biol
  doi: 10.1128/MCB.23.2.474-481.2003
– volume: 99
  start-page: 247
  year: 1999
  ident: 1901_CR25
  publication-title: Cell
  doi: 10.1016/S0092-8674(00)81656-6
– volume: 445
  start-page: 168
  year: 2007
  ident: 1901_CR28
  publication-title: Nature
  doi: 10.1038/nature05453
– reference: 12297046 - Cell. 2002 Sep 20;110(6):725-35
– reference: 16420703 - BMC Evol Biol. 2006;6:5
– reference: 8833448 - Annu Rev Neurosci. 1996;19:379-404
– reference: 17190607 - Cell. 2006 Dec 29;127(7):1453-67
– reference: 16098631 - Trends Genet. 2005 Oct;21(10):536-9
– reference: 15967424 - Dev Biol. 2005 Jul 15;283(2):522-34
– reference: 11773596 - Physiol Genomics. 2001 Dec 21;7(2):97-104
– reference: 12364792 - Science. 2002 Oct 4;298(5591):149-59
– reference: 17510324 - Science. 2007 Jun 22;316(5832):1718-23
– reference: 15876192 - Evol Dev. 2005 May-Jun;7(3):196-200
– reference: 10467576 - Learn Mem. 1995 Sep-Oct;2(5):199-224
– reference: 12297045 - Cell. 2002 Sep 20;110(6):713-23
– reference: 15591204 - Science. 2004 Dec 10;306(5703):1937-40
– reference: 17073008 - Nature. 2006 Oct 26;443(7114):931-49
– reference: 18021399 - Genome Biol. 2007;8(11):R242
– reference: 9647634 - Genome Res. 1998 Jun;8(6):590-8
– reference: 12481130 - Science. 2002 Dec 13;298(5601):2157-67
– reference: 12944428 - Development. 2003 Nov;130(21):5083-90
– reference: 11166636 - Trends Cogn Sci. 2001 Feb 1;5(2):62-71
– reference: 16723033 - Genome Biol. 2006;7(5):R43
– reference: 15650739 - Nature. 2005 Jan 13;433(7022):156-60
– reference: 16128622 - PLoS Biol. 2005 Oct;3(10):e314
– reference: 12787557 - Cytokine Growth Factor Rev. 2003 Jun-Aug;14(3-4):181-4
– reference: 12509447 - Mol Cell Biol. 2003 Jan;23(2):474-81
– reference: 18362917 - Nature. 2008 Apr 24;452(7190):949-55
– reference: 14595094 - Mol Biol Evol. 2004 Feb;21(2):236-9
– reference: 18243095 - Cell. 2008 Jan 25;132(2):185-95
– reference: 14506234 - J Biol Chem. 2003 Dec 5;278(49):49031-43
– reference: 1498330 - Blood. 1992 Aug 15;80(4):879-86
– reference: 12952880 - Genome Res. 2003 Sep;13(9):2118-28
– reference: 14680636 - Curr Biol. 2003 Dec 16;13(24):2190-5
– reference: 17151600 - Nature. 2007 Jan 11;445(7124):168-76
– reference: 12364791 - Science. 2002 Oct 4;298(5591):129-49
– reference: 12151402 - J Biol Chem. 2002 Oct 11;277(41):38358-63
– reference: 17068262 - Science. 2006 Oct 27;314(5799):645-7
– reference: 10555141 - Cell. 1999 Oct 29;99(3):247-57
– reference: 16311335 - Science. 2005 Nov 25;310(5752):1325-6
– reference: 17994087 - Nature. 2007 Nov 8;450(7167):203-18
– reference: 16226338 - Trends Genet. 2005 Dec;21(12):633-9
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Snippet Background Large-scale comparison of metazoan genomes has revealed that a significant fraction of genes of the last common ancestor of Bilateria (Urbilateria)...
Large-scale comparison of metazoan genomes has revealed that a significant fraction of genes of the last common ancestor of Bilateria (Urbilateria) is lost in...
Abstract Background Large-scale comparison of metazoan genomes has revealed that a significant fraction of genes of the last common ancestor of Bilateria...
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StartPage 17
SubjectTerms Animal Genetics and Genomics
Animals
Bees
Bees - genetics
Bilateria
Biological diversity
Biological Evolution
Biomedical and Life Sciences
Biotechnology
Brain
Brain - metabolism
Evolution
Gene expression
Gene Expression Profiling
Genes, Insect
Genetic aspects
Genetics
Genomics
Honeybee
info:eu-repo/classification/ddc/576.5
Life Sciences
Mice
Mice - genetics
Microarrays
Microbial Genetics and Genomics
Plant Genetics and Genomics
Proteomics
QH426-470
Research Article
RNA
RNA - genetics
Species Specificity
TP248.13-248.65
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Title Expression profiles of urbilaterian genes uniquely shared between honey bee and vertebrates
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