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Photomorphogenesis

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484:) Exposure to UV- light in plants mediates biochemical pathways, photosynthesis, plant growth and many other processes essential to plant development. The UV-B photoreceptor, UV Resistance Locus8 (UVR8) detects UV-B rays and elicits photomorphogenic responses. These response are important for initiating hypocotyl elongation, leaf expansion, biosynthesis of flavonoids and many other important processes that affect the root-shoot system. Exposure to UV-B rays can be damaging to DNA inside of the plant cells, however, UVR8 induces genes required to acclimate plants to UV-B radiation, these genes are responsible for many biosynthesis pathways that involve protection from UV damage, oxidative stress, and photorepair of DNA damage. 191: 437:, an enzyme that carries out light-dependent repair of UV damaged DNA. There are two different forms of cryptochromes that have been identified in plants, CRY1 and CRY2, which regulate the inhibition of hypocotyl elongation in response to blue light. Cryptochromes control stem elongation, leaf expansion, circadian rhythms and flowering time. In addition to blue light, cryptochromes also perceive long wavelength 357:, an apoprotein combined with its prosthetic group, becomes sensitive to light. If it absorbs red light it will change conformation to the biologically active Pfr form. The Pfr form can absorb far red light and switch back to the Pr form. The Pfr promotes and regulates photomorphogenesis in response to FR light, whereas Pr regulates de-etiolation in response to R light. 374:. PHYA is involved in the regulation of photomorphogenesis in response to far-red light. PHYB is involved in regulating photoreversible seed germination in response to red light. PHYC mediates the response between PHYA and PHYB. PHYD and PHYE mediate elongation of the internode and control the time in which the plant flowers. 328:
to detect and respond to red and far-red wavelengths. Phytochromes are signaling proteins that promote photomorphogenesis in response to red light and far-red light. Phytochrome is the only known photoreceptor that absorbs light in the red/far red spectrum of light (600-750 nm) specifically and
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appears as the root becomes established. Later, with growth of the shoot (particularly when it emerges into the light) there is increased secondary root formation and branching. In this coordinated progression of developmental responses are early manifestations of correlative growth phenomena where
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and involves using red photoreceptors (phytochromes) to determine the daylength. As a result, photoperiodic plants only start making flowers when the days have reached a "critical daylength," allowing these plants to initiate their flowering period according to the time of year. For example, "long
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There are two forms of phytochromes: red light absorbing, Pr, and far-red light absorbing, Pfr. Pfr, which is the active form of phytochromes, can be reverted to Pr, which is the inactive form, slowly by inducing darkness or more rapidly by irradiation by far-red light. The phytochrome
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There is still much to be discovered about the mechanisms involved in UV-B radiation and UVR8. Scientists are working to understand the pathways responsible for plant UV receptors response to solar radiation in natural environments.
364:. The different forms of phytochrome control different responses but there is also redundancy so that in the absence of one phytochrome, another may take on the missing functions. There are five genes that encode phytochromes in the 291:
Photoperiodism also has an effect on vegetative growth, including on bud dormancy in perennial plants, though this is not as well-documented as the effect of photoperiodism on the switch to the flowering stage.
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to grow the plants. There are at least three stages of plant development where photomorphogenesis occurs: seed germination, seedling development, and the switch from the vegetative to the flowering stage
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it was the opposite, where far-red light exposure caused the root tips to adhere, and red light caused the roots to detach. This effect of red and far-red light on root tips is now known as the
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were the first blue light receptors to be isolated and characterized from any organism, and are responsible for the blue light reactions in photomorphogenesis. The proteins use a
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Typically, plants are responsive to wavelengths of light in the blue, red and far-red regions of the spectrum through the action of several different photosensory systems. The
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Some plants rely on light signals to determine when to switch from the vegetative to the flowering stage of plant development. This type of photomorphogenesis is known as
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Aphalo, Pedro J.; Tegelberg, Riitta; Lindfors, Anders V.; Strid, Åke; Sipari, Nina; Wargent, Jason J.; Jenkins, Gareth I.; Vainonen, Julia; Brosché, Mikael (2013-02-01).
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introduced the term "etiolement" to the scientific literature in 1754 when describing his experiments, commenting that the term was already in use by gardeners.
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adhered to the sides of a beaker with a negatively charged surface after being treated with red light, yet released after being exposed to far-red light. For
178:(dark development), which is characterized by etiolation. Upon exposure to light, the seedling switches rapidly to photomorphogenesis (light development). 175: 316:. The combination of phytochromes and cryptochromes mediate growth and the flowering of plants in response to red light, far-red light, and blue light. 1110:"Multiple Roles for UV Resistance Locus8 in Regulating Gene Expression and Metabolite Accumulation in Arabidopsis under Solar Ultraviolet Radiation" 243: 205: 423:
and molecular analyses, it has been determined that higher plants contain at least 4, and probably 5, different blue light photoreceptors.
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day" plants need long days to start flowering, and "short day" plants need to experience short days before they will start making flowers.
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A dicot seedling emerging from the ground displays an apical hook (in the hypocotyl in this case), a response to dark conditions
635: 581: 28:-mediated development, where plant growth patterns respond to the light spectrum. This is a completely separate process from 102:(371 to 287 BC) may have been the first to write about photomorphogenesis. He described the different wood qualities of 275:
The developmental changes characteristic of photomorphogenesis shown by de-etiolated seedlings, are induced by light.
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Light has profound effects on the development of plants. The most striking effects of light are observed when a
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only for photosensory purposes. Phytochromes are proteins with a light absorbing pigment attached called a
308:. There are at least 5 members of the phytochrome family of photoreceptors. There are several blue light 1185: 468:
has been shown to be a UV-B receptor. Plants undergo distinct photomorphogenic changes as a result of
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the root affects the growth of the shoot and vice versa. To a large degree, the growth responses are
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irradiation (UV-A). Since the cryptochromes were discovered in plants, several labs have identified
345:, a protein that together with a prosthetic group forms a particular biochemical molecule such as a 181:
There are differences when comparing dark-grown (etiolated) and light-grown (de-etiolated) seedlings
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Photobiological Sciences Online. Resources available from the American Society for Photobiology
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of the seedling causes it to become elongated, which may facilitate it emerging from the soil.
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Most research on photomorphogenesis is derived from plants studies involving several kingdoms:
784:"A Rapid Photoreversible Response of Barely Root Tips in the Presence of 3-Indoleacetic Acid" 472:
radiation. They have photoreceptors that initiate morphogenetic changes in the plant embryo (
381:(ferns, mosses, algae) and photosynthetic bacteria have shown that phytochromes evolved from 40:
are photochromic sensory receptors that restrict the photomorphogenic effect of light to the
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There are blue light photoreceptors that are not a part of photomorphogenesis. For example,
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genes and photoreceptors in a number of other organisms, including humans, mice and flies.
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Photomorphogenesis in Plants and Bacteria: Function and Signal Transduction Mechanisms
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Proceedings of the National Academy of Sciences of the United States of America
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grown in different levels of light, likely the result of the photomorphogenic "
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A seedling that emerges in darkness follows a developmental program known as
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seedling emerges from the soil and is exposed to light for the first time.
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as a chromophore. The cryptochromes have evolved from microbial DNA-
576:. Springer Science & Business Media. pp. 4, 178, 183–184. 477: 353:, is synthesized in the Pr form. Upon binding the chromophore, the 111: 84: 653:"From Darkness into Light: Factors Controlling Photomorphogenesis" 481: 420: 346: 190: 152: 143: 88: 377:
Molecular analyses of phytochrome and phytochrome-like genes in
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Most plants have multiple phytochromes encoded by different
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wrote "Historia Plantarum" which mentioned the effects of
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where light is used as a source of energy. Phytochromes,
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Taiz, Lincoln; Zeiger, Eduardo; Møller, Ian Max (2015).
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which have different functions. Based on studies with
1057:"Photomorphogenic responses to ultraviolet-B light" 1007:"Photomorphogenic responses to ultraviolet-B light" 619: 617: 385:photoreceptors that predated the origin of plants. 333:. The chromophore is a linear tetrapyrrole called 1177: 766: 614: 125: 452:is the blue light photoreceptor that controls 304:for red and far-red wavelengths are known as 954:Ulm, Roman; Jenkins, Gareth I (2015-06-30). 146:(root) emerges first from the seed, and the 464:Plants show various responses to UV light. 163:In the absence of light, plants develop an 953: 565: 563: 561: 52:portions of the electromagnetic spectrum. 1141: 981: 971: 930: 874: 817: 799: 736: 684: 569: 541: 624:Eberhard Schc$ fer; Ferenc Nagy (2006). 189: 1054: 1004: 907:"The Cryptochrome Blue Light Receptors" 650: 558: 158: 1178: 840: 781: 762: 760: 758: 756: 296:Light receptors for photomorphogenesis 1103: 1101: 900: 898: 896: 894: 507: 706: 704: 702: 700: 698: 696: 510:"The Red Side of Photomorphogenesis" 503: 501: 319: 271:Lateral root development accelerated 753: 411:Plants contain multiple blue light 233:Limited production of lateral roots 130: 13: 1098: 904: 891: 713:"Phytochrome Signaling Mechanisms" 710: 59:is often studied by using tightly 14: 1197: 1162: 1055:Jenkins, Gareth I. (2017-11-01). 1005:Jenkins, Gareth I. (2017-11-01). 693: 498: 278: 905:Yu, Xuhong; et al. (2010). 769:Plant Physiology and Development 711:Li, Jigang; et al. (2011). 651:Eckardt, Nancy A. (2001-02-01). 227:Limited radial expansion of stem 118:(grow in the absence of light). 1048: 998: 947: 391:observed that the root tips of 834: 775: 644: 590: 573:Lectures on Photomorphogenesis 508:Parks, Brian M. (2003-12-01). 1: 1064:Plant, Cell & Environment 1014:Plant, Cell & Environment 782:Tanada, Takuma (1968-02-01). 570:Hans Mohr (6 December 2012). 491: 406: 238:De-etiolated characteristics: 126:Developmental stages affected 7: 459: 10: 1202: 262:Stem elongation suppressed 199:Etiolated characteristics: 183: 94: 55:The photomorphogenesis of 973:10.1186/s12915-015-0156-y 841:Tanada, T. (1972-01-01). 268:Root elongation promoted 265:Radial expansion of stem 230:Limited root elongation 195: 142:Normally the seedling 100:Theophrastus of Eresus 1126:10.1104/pp.112.211375 801:10.1073/pnas.59.2.376 526:10.1104/pp.103.029702 224:Rapid stem elongation 193: 18:developmental biology 911:The Arabidopsis Book 717:The Arabidopsis Book 669:10.1105/tpc.13.2.219 598:"Photomorphogenesis" 367:Arabidopsis thaliana 253:Leaf growth promoted 159:Seedling development 859:10.1104/pp.49.4.560 196: 176:skotomorphogenesis 22:photomorphogenesis 1186:Plant development 1076:10.1111/pce.12934 1070:(11): 2544–2557. 1026:10.1111/pce.12934 1020:(11): 2544–2557. 637:978-1-4020-3809-9 602:photobiology.info 583:978-3-642-65418-3 320:Red/far-red light 110:effect. In 1686, 1193: 1172: 1156: 1155: 1145: 1114:Plant Physiology 1105: 1096: 1095: 1061: 1052: 1046: 1045: 1011: 1002: 996: 995: 985: 975: 951: 945: 944: 934: 923:10.1199/tab.0135 902: 889: 888: 878: 847:Plant Physiology 838: 832: 831: 821: 803: 779: 773: 772: 764: 751: 750: 740: 729:10.1199/tab.0148 708: 691: 690: 688: 648: 642: 641: 621: 612: 611: 609: 608: 594: 588: 587: 567: 556: 555: 545: 520:(4): 1437–1444. 514:Plant Physiology 505: 335:phytochromobilin 167:growth pattern. 131:Seed germination 108:shade-avoidance" 1201: 1200: 1196: 1195: 1194: 1192: 1191: 1190: 1176: 1175: 1168: 1165: 1160: 1159: 1106: 1099: 1059: 1053: 1049: 1009: 1003: 999: 952: 948: 903: 892: 839: 835: 780: 776: 765: 754: 709: 694: 649: 645: 638: 622: 615: 606: 604: 596: 595: 591: 584: 568: 559: 506: 499: 494: 462: 409: 370:genetic model, 322: 298: 281: 188: 161: 133: 128: 97: 12: 11: 5: 1199: 1189: 1188: 1174: 1173: 1164: 1163:External links 1161: 1158: 1157: 1120:(2): 744–759. 1097: 1047: 997: 946: 890: 853:(4): 560–562. 833: 794:(2): 376–380. 774: 752: 692: 663:(2): 219–221. 657:The Plant Cell 643: 636: 613: 589: 582: 557: 496: 495: 493: 490: 461: 458: 417:action spectra 413:photoreceptors 408: 405: 321: 318: 310:photoreceptors 302:photoreceptors 297: 294: 285:photoperiodism 280: 279:Photoperiodism 277: 273: 272: 269: 266: 263: 260: 254: 251: 235: 234: 231: 228: 225: 222: 216: 215:No leaf growth 213: 160: 157: 132: 129: 127: 124: 120:Charles Bonnet 96: 93: 70:photoperiodism 30:photosynthesis 9: 6: 4: 3: 2: 1198: 1187: 1184: 1183: 1181: 1171: 1167: 1166: 1153: 1149: 1144: 1139: 1135: 1131: 1127: 1123: 1119: 1115: 1111: 1104: 1102: 1093: 1089: 1085: 1081: 1077: 1073: 1069: 1065: 1058: 1051: 1043: 1039: 1035: 1031: 1027: 1023: 1019: 1015: 1008: 1001: 993: 989: 984: 979: 974: 969: 965: 961: 957: 950: 942: 938: 933: 928: 924: 920: 916: 912: 908: 901: 899: 897: 895: 886: 882: 877: 872: 868: 864: 860: 856: 852: 848: 844: 837: 829: 825: 820: 815: 811: 807: 802: 797: 793: 789: 785: 778: 770: 763: 761: 759: 757: 748: 744: 739: 734: 730: 726: 722: 718: 714: 707: 705: 703: 701: 699: 697: 687: 682: 678: 674: 670: 666: 662: 658: 654: 647: 639: 633: 629: 628: 620: 618: 603: 599: 593: 585: 579: 575: 574: 566: 564: 562: 553: 549: 544: 539: 535: 531: 527: 523: 519: 515: 511: 504: 502: 497: 489: 485: 483: 479: 475: 471: 467: 457: 455: 451: 446: 444: 440: 436: 432: 428: 427:Cryptochromes 424: 422: 418: 414: 404: 402: 401:Tanada effect 398: 394: 390: 389:Takuma Tanada 386: 384: 380: 379:higher plants 375: 373: 369: 368: 363: 358: 356: 352: 348: 344: 338: 336: 332: 327: 317: 315: 314:cryptochromes 311: 307: 303: 293: 289: 286: 276: 270: 267: 264: 261: 258: 255: 252: 249: 245: 242: 241: 240: 239: 232: 229: 226: 223: 221: 217: 214: 211: 207: 203: 202: 201: 200: 192: 187: 182: 179: 177: 172: 170: 166: 156: 154: 149: 145: 140: 138: 123: 121: 117: 113: 109: 105: 101: 92: 90: 86: 82: 78: 73: 71: 66: 65:light sources 62: 58: 53: 51: 50:blue, and red 47: 43: 39: 35: 34:cryptochromes 31: 27: 23: 19: 1117: 1113: 1067: 1063: 1050: 1017: 1013: 1000: 963: 959: 949: 917:(8): e0135. 914: 910: 850: 846: 836: 791: 787: 777: 768: 720: 716: 660: 656: 646: 626: 605:. Retrieved 601: 592: 572: 517: 513: 486: 463: 454:phototropism 447: 425: 410: 387: 376: 371: 365: 359: 339: 323: 306:phytochromes 299: 290: 282: 274: 237: 236: 198: 197: 180: 173: 162: 141: 134: 98: 74: 63:-controlled 54: 38:phototropins 21: 15: 960:BMC Biology 450:phototropin 383:prokaryotic 355:holoprotein 331:chromophore 326:phytochrome 324:Plants use 257:Chlorophyll 250:splits open 244:Apical hook 220:chlorophyll 208:(dicot) or 206:apical hook 137:germinating 607:2018-12-07 492:References 443:homologous 435:photolyase 407:Blue light 343:apoprotein 248:coleoptile 210:coleoptile 186:Etiolation 184:See also: 169:Etiolation 155:mediated. 116:etiolation 1134:1532-2548 1084:1365-3040 1034:1365-3040 966:(1): 45. 810:0027-8424 723:: e0148. 677:1532-298X 534:1532-2548 474:hypocotyl 397:mung bean 372:PHYA-PHYE 312:known as 246:opens or 212:(monocot) 204:Distinct 165:etiolated 104:fir trees 61:frequency 1180:Category 1152:23250626 1092:28183154 1042:28183154 992:26123292 941:21841916 885:16658001 828:16591610 747:22303272 552:14681526 478:epicotyl 460:UV light 259:produced 112:John Ray 85:Protista 1143:3561016 983:4484705 932:3155252 867:4262772 738:3268501 686:1464706 543:1540344 482:radicle 421:mutants 347:hormone 153:hormone 144:radicle 95:History 89:Plantae 1150:  1140:  1132:  1090:  1082:  1040:  1032:  990:  980:  939:  929:  883:  876:366005 873:  865:  826:  819:224682 816:  808:  745:  735:  683:  675:  634:  580:  550:  540:  532:  431:flavin 393:barley 351:enzyme 87:, and 81:Monera 57:plants 36:, and 1060:(PDF) 1010:(PDF) 863:JSTOR 362:genes 148:shoot 77:Fungi 26:light 1148:PMID 1130:ISSN 1088:PMID 1080:ISSN 1038:PMID 1030:ISSN 988:PMID 937:PMID 881:PMID 824:PMID 806:ISSN 743:PMID 673:ISSN 632:ISBN 578:ISBN 548:PMID 530:ISSN 470:UV-B 466:UVR8 46:UV-B 42:UV-A 1138:PMC 1122:doi 1118:161 1072:doi 1022:doi 978:PMC 968:doi 927:PMC 919:doi 871:PMC 855:doi 814:PMC 796:doi 733:PMC 725:doi 681:PMC 665:doi 538:PMC 522:doi 518:133 349:or 218:No 72:). 24:is 16:In 1182:: 1146:. 1136:. 1128:. 1116:. 1112:. 1100:^ 1086:. 1078:. 1068:40 1066:. 1062:. 1036:. 1028:. 1018:40 1016:. 1012:. 986:. 976:. 964:13 962:. 958:. 935:. 925:. 913:. 909:. 893:^ 879:. 869:. 861:. 851:49 849:. 845:. 822:. 812:. 804:. 792:59 790:. 786:. 755:^ 741:. 731:. 719:. 715:. 695:^ 679:. 671:. 661:13 659:. 655:. 616:^ 600:. 560:^ 546:. 536:. 528:. 516:. 512:. 500:^ 480:, 476:, 456:. 439:UV 419:, 403:. 337:. 91:. 83:, 79:, 48:, 44:, 20:, 1154:. 1124:: 1094:. 1074:: 1044:. 1024:: 994:. 970:: 943:. 921:: 915:8 887:. 857:: 830:. 798:: 749:. 727:: 721:9 689:. 667:: 640:. 610:. 586:. 554:. 524:: 68:(

Index

developmental biology
light
photosynthesis
cryptochromes
phototropins
UV-A
UV-B
blue, and red
plants
frequency
light sources
photoperiodism
Fungi
Monera
Protista
Plantae
Theophrastus of Eresus
fir trees
shade-avoidance"
John Ray
etiolation
Charles Bonnet
germinating
radicle
shoot
hormone
etiolated
Etiolation
skotomorphogenesis
Etiolation

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