Floral variation and floral genetics in basal angiosperms
Recent advances in phylogeny reconstruction and floral genetics set the stage for new investigations of the origin and diversification of the flower. We review the current state of angiosperm phylogeny, with an emphasis on basal lineages. With the surprising inclusion of Hydatellaceae with Nymphaeal...
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Veröffentlicht in: | American journal of botany 2009, Vol.96 (1), p.110-128 |
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description | Recent advances in phylogeny reconstruction and floral genetics set the stage for new investigations of the origin and diversification of the flower. We review the current state of angiosperm phylogeny, with an emphasis on basal lineages. With the surprising inclusion of Hydatellaceae with Nymphaeales, recent studies support the topology of Amborella sister to all other extant angiosperms, with Nymphaeales and then Austrobaileyales as subsequent sisters to all remaining angiosperms. Notable modifications from most recent analyses are the sister relationships of Chloranthaceae with the magnoliids and of Ceratophyllaceae with eudicots. We review "trends" in floral morphology and contrast historical, intuitive interpretations with explicit character-state reconstructions using molecular-based trees, focusing on (1) the size, number, and organization of floral organs; (2) the evolution of the perianth; (3) floral symmetry; and (4) floral synorganization. We provide summaries of those genes known to affect floral features that contribute to much of floral diversity. Although most floral genes have not been investigated outside of a few model systems, sufficient information is emerging to identify candidate genes for testing specific hypotheses in nonmodel plants. We conclude with a set of evo-devo case studies in which floral genetics have been linked to variation in floral morphology. |
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We review the current state of angiosperm phylogeny, with an emphasis on basal lineages. With the surprising inclusion of Hydatellaceae with Nymphaeales, recent studies support the topology of Amborella sister to all other extant angiosperms, with Nymphaeales and then Austrobaileyales as subsequent sisters to all remaining angiosperms. Notable modifications from most recent analyses are the sister relationships of Chloranthaceae with the magnoliids and of Ceratophyllaceae with eudicots. We review "trends" in floral morphology and contrast historical, intuitive interpretations with explicit character-state reconstructions using molecular-based trees, focusing on (1) the size, number, and organization of floral organs; (2) the evolution of the perianth; (3) floral symmetry; and (4) floral synorganization. We provide summaries of those genes known to affect floral features that contribute to much of floral diversity. Although most floral genes have not been investigated outside of a few model systems, sufficient information is emerging to identify candidate genes for testing specific hypotheses in nonmodel plants. We conclude with a set of evo-devo case studies in which floral genetics have been linked to variation in floral morphology.</description><identifier>ISSN: 0002-9122</identifier><identifier>EISSN: 1537-2197</identifier><identifier>DOI: 10.3732/ajb.0800182</identifier><identifier>PMID: 21628179</identifier><identifier>CODEN: AJBOAA</identifier><language>eng</language><publisher>United States: Botanical Society of America</publisher><subject>ABC model ; Angiosperms ; basal angiosperms ; Biodiversity ; Botany ; Evolution ; Evolutionary biology ; Evolutionary genetics ; evo‐devo ; Flowers & plants ; Genes ; Genetics ; perianth evolution ; Perianths ; Petals ; Phylogenetics ; Phylogeny ; Plant reproduction ; Plants ; Special Invited Papers ; Stamens ; symmetry ; synorganization</subject><ispartof>American journal of botany, 2009, Vol.96 (1), p.110-128</ispartof><rights>Copyright 2009 Botanical Society of America, Inc.</rights><rights>2009 Botanical Society of America</rights><rights>Copyright Botanical Society of America, Inc. 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We review the current state of angiosperm phylogeny, with an emphasis on basal lineages. With the surprising inclusion of Hydatellaceae with Nymphaeales, recent studies support the topology of Amborella sister to all other extant angiosperms, with Nymphaeales and then Austrobaileyales as subsequent sisters to all remaining angiosperms. Notable modifications from most recent analyses are the sister relationships of Chloranthaceae with the magnoliids and of Ceratophyllaceae with eudicots. We review "trends" in floral morphology and contrast historical, intuitive interpretations with explicit character-state reconstructions using molecular-based trees, focusing on (1) the size, number, and organization of floral organs; (2) the evolution of the perianth; (3) floral symmetry; and (4) floral synorganization. We provide summaries of those genes known to affect floral features that contribute to much of floral diversity. Although most floral genes have not been investigated outside of a few model systems, sufficient information is emerging to identify candidate genes for testing specific hypotheses in nonmodel plants. We conclude with a set of evo-devo case studies in which floral genetics have been linked to variation in floral morphology.</description><subject>ABC model</subject><subject>Angiosperms</subject><subject>basal angiosperms</subject><subject>Biodiversity</subject><subject>Botany</subject><subject>Evolution</subject><subject>Evolutionary biology</subject><subject>Evolutionary genetics</subject><subject>evo‐devo</subject><subject>Flowers & plants</subject><subject>Genes</subject><subject>Genetics</subject><subject>perianth evolution</subject><subject>Perianths</subject><subject>Petals</subject><subject>Phylogenetics</subject><subject>Phylogeny</subject><subject>Plant reproduction</subject><subject>Plants</subject><subject>Special Invited Papers</subject><subject>Stamens</subject><subject>symmetry</subject><subject>synorganization</subject><issn>0002-9122</issn><issn>1537-2197</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kEFv1DAQRi1ERbeFE2cgqoQ4oJQZO4ntY1tRCqrEAXq2Jo6z9SqJF3uXqP--RllA4sDJ8sybN6OPsZcI50IK_oE27TkoAFT8CVthLWTJUcunbAUAvNTI-TE7SWmTv7rS_Bk75thwhVKvmL4eQqSh-EnR086HqaCpK_qluHaT23mbCj8VLaVcoWntQ9q6OKbn7KinIbkXh_eU3V1__H51U95-_fT56uK2tLVooMQOVd9B11Vt3bW6tb2wQE1rpcQWrNZkG6DOVVYQF2QzIlzNeaVVg7aT4pS9W7zbGH7sXdqZ0SfrhoEmF_bJqEZL3UClM3n2D7kJ-zjl4wzHWimpdJWh9wtkY0gput5sox8pPhgE8ytPk_M0hzwz_fqg3Lej6_6wvwPMAC7A7Af38D-XufhyyQER8syrZWaTdiH-dcrsA6ly_-3Sv_fr-9lHZ9JIw5BPQDPPs24MmsXzZuF6CobW0Sdz9y2vEIC11FwL8QjdTp6D</recordid><startdate>2009</startdate><enddate>2009</enddate><creator>Soltis, Pamela S</creator><creator>Brockington, Samuel F</creator><creator>Yoo, Mi-Jeong</creator><creator>Piedrahita, Ana</creator><creator>Latvis, Maribeth</creator><creator>Moore, Michael J</creator><creator>Chanderbali, Andre S</creator><creator>Soltis, Douglas E</creator><general>Botanical Society of America</general><general>Botanical Soc America</general><general>Botanical Society of America, Inc</general><scope>FBQ</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope></search><sort><creationdate>2009</creationdate><title>Floral variation and floral genetics in basal angiosperms</title><author>Soltis, Pamela S ; 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subjects | ABC model Angiosperms basal angiosperms Biodiversity Botany Evolution Evolutionary biology Evolutionary genetics evo‐devo Flowers & plants Genes Genetics perianth evolution Perianths Petals Phylogenetics Phylogeny Plant reproduction Plants Special Invited Papers Stamens symmetry synorganization |
title | Floral variation and floral genetics in basal angiosperms |
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