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Zootermopsis nevadensis

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546:. There were identified four Vgs. Two of them seem to be recent tandem duplications pretty conserved. One of these duplications is closely related to Neofem3 a specific gene implied in reproduction in other termite species. Three of the Four Vgs are significantly expressed in reproductive queens. One of the Vgs genes is moderately expressed in nymphs and non-reproductive workers. Vgs seem to have acquired a role in the regulation of caste behaviour. Overexpression of Vgs plays an important role as antioxidant and this feature could participate in reproductive females' longevity. 135: 711:
Mitchell, Robert D.; Munoz-Torres, Monica C.; Mustard, Julie A.; Pan, Hailin; Reese, Justin T.; Scharf, Michael E.; Sun, Fengming; Vogel, Heiko; Xiao, Jin; Yang, Wei; Yang, Zhikai; Yang, Zuoquan; Zhou, Jiajian; Zhu, Jiwei; Brent, Colin S.; Elsik, Christine G.; Goodisman, Michael A. D.; Liberles, David A.; Roe, R. Michael; Vargo, Edward L.; Vilcinskas, Andreas; Wang, Jun; Bornberg-Bauer, Erich; Korb, Judith; Zhang, Guojie; Liebig, Jürgen (20 May 2014). "Molecular traces of alternative social organization in a termite genome".
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Homogeneous populations living in high density are perfect targets for infections. This termite concretely lives in a pathogen-rich environment. The genome was analyzed in order to establish the relationship between eusociality and disease resistance. There were found all the vias related to immunity
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Among gene families with a significant expansion, four of them exhibit overexpression on fertile males and they are linked to male spermatogenesis or cellular division: Kelch-like proteins 10 (KLHL10) and Seven-in-abstenia (SINA). The codified proteins are associated with E3-ubiquitine-ligase complex
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Terrapon, Nicolas; Li, Cai; Robertson, Hugh M.; Ji, Lu; Meng, Xuehong; Booth, Warren; Chen, Zhensheng; Childers, Christopher P.; Glastad, Karl M.; Gokhale, Kaustubh; Gowin, Johannes; Gronenberg, Wulfila; Hermansen, Russell A.; Hu, Haofu; Hunt, Brendan G.; Huylmans, Ann Kathrin; Khalil, Sayed M. S.;
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Terrapon, N.; Li, C.; Robertson, H. M.; Ji, L.; Meng, X.; Booth, W.; Chen, Z.; Childers, C. P.; Glastad, K. M.; Gokhale, K.; Gowin, J.; Gronenberg, W.; Hermansen, R. A.; Hu, H.; Hunt, B. G.; Huylmans, A. K.; Khalil, S. M. S.; Mitchell, R. D.; Munoz-Torres, M. C.; Mustard, J. A.; Pan, H.; Reese, J.
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are haeme-thiolate enzymes. In insects they contribute in endogenous and xenobiotics compound degradation. CYP4 and CYP5 families are implied in JH synthesis and degradation. CYP450 is involved with the JH-dependent differentiation from worker to soldier termites. There were found 55 CYP450 genes.
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The differentiation in castes and the reproductive division of labor is a marker of insect eusociality. Within Hymenoptera it has been proposed some regulators including vitelogenines (Vgs), juvenile hormone (JH), biogenic amines and other regulator like juvenile hormone binding proteins and some
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has a limited ability to discriminate odours. The majority of the termites live their lives within a single log. A colony rarely meet other termites outside the log. In the other hand eusocial insects like bees has a developed sense of smell. This feature provide bees a sophisticated weapon to
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shows expansion on genes implied in chemical communication, a crucial component in insects societies. It has approximately 280 functional chemoreceptor genes. This number is over the average of insects, but intermediate among ants or bees. Although the total number of genes is comparable, its
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are involved in insect development, reproduction, longevity and both solitary and social behaviour. In termites it is well known that JHs module caste differentiation and adult gonadal activity. JHs have different functions among development stages and a lot of different functions within a
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implicated in espermatide proteins degradation. There are other gene families which are not expanded but shows a differential expression pattern among developmental stages and castes. Collectively, the data suggest an expanded role around spermatogenesis regulation and termite evolution.
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is formed by glomeruli. The glomeruli are tightly packed and they are composed by terminal axons projected from receptor neurons to the antennae. The sensor neurons which express the same chemoreceptors extend their axons to the same glomeruli.
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genome was to find molecular traces of eusociality. The authors compared the whole sequenced and assembled genome and 25 transcriptomes from different development states and castes with the already sequenced genomes of eusocial
632:. Two of them are implicated in JH availability. Hexamerins reduce the JH availability in workers and nymphal stages. The overexpression during this plastic stages inhibits the differentiation to soldiers. 508:, more than in other insects. One of them is specific of insect and the rest are specific of termites. This feature means that this kind of genes were expanded early within the evolution of this species. 764:
Masuoka, Yudai; Yaguchi, Hajime; Suzuki, Ryutaro; Maekawa, Kiyoto (September 2015). "Knockdown of the juvenile hormone receptor gene inhibits soldier-specific morphogenesis in the damp-wood termite
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3 antimicrobian peptides (AMPs) (attacin, dipericine and a termicine ortologue). It was unexpected because the ant response against living in a pathogen rich environment is the expansion of AMPs.
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only has 72 glomeruli, the majority of them are joined to the 63 ORs. As a result, only a few number of IRs and GRs are implied in olfaction, the rest may be implied in gustation. The termite
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signaling pathways like insulin/insulin growth factor and yellow/major royal jelly protein like genes. The main genes involved in the reproductive division of labor are:
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one of each group is highly expressed in reproductive forms. The reproductive co-expression of these genes makes them hydrocarbon signaling regulators candidates in
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there was found all the enzymes of the JHIII biosynthetic pathway and major regulators such as JH-binding proteins impact caste differentiation.
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mate repeatedly during the mature stage and need to increase sperm production. Moreover, males activate and deactivate their testes cyclically.
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Liebig, Jürgen; Eliyahu, Dorit; Brent, Colin S. (October 2009). "Cuticular hydrocarbon profiles indicate reproductive status in the termite
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take part in lifespan regulation. There was found two histone-deacetylases overexpressed in reproductive females, sirtuin 6 and sirtuin 7.
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genes copies, the smallest number of opsin genes known among the insects, as a result of living in the dark for tens of millions of years.
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Cornette, R.; Koshikawa, S.; Hojo, M.; Matsumoto, T.; Miura, T. (April 2006). "Caste-specific cytochrome P450 in the damp-wood termite
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Pathogens play an important role in eusocial insects, but the mechanisms improved to combat them differs in a taxon-specific manner.
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is directed by the abundance of four long chain polyunsaturated alkenes. From 16 elongases and 10 desaturases found in
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in Drosophila and other insects, including pattern recognition receptors, signaling pathways and regulatory genes.
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The great difference between ORs and IRs gives an opportunity to study the organization of the olfactive lobe. The
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T.; Scharf, M. E.; Sun, F.; Vogel, H.; Xiao, J.; Yang, W.; Yang, Z.; Yang, Z.; et al. (2014).
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The reproductive division of labor is associated with an increased longevity of reproductives and
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distribution within different gene families diverge from what has been observed in Hymenoptera.
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The Nevada termite lives in central and central-east California, and in central-west Nevada.
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are usually storage proteins in solitary insects. There were found 5 hexamerin genes in
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In eusocial insects and the reproductive division of labor is regulated by
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Male termites complete gamete maturation after their moult. Male
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Male reproductive soldier (top) and male soldier (bottom) of
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It is a 513:signaling pathway genes related to immune system 8: 894: 618:, but intermediate compared with eusocial 515:are overexpressed in reproductive females. 465:are implied in gustation and olfaction in 133: 122: 770:Insect Biochemistry and Molecular Biology 740: 686: 676: 606:are implicated in caste differentiation. 109:Learn how and when to remove this message 642: 538:are precursors of the egg yolk protein 614:This number is lower than in solitary 506:Gram-negative binding proteins (GNBPs) 7: 47:adding citations to reliable sources 817:Behavioral Ecology and Sociobiology 367:The Nevada termite is preyed on by 319:is subdivided into two subspecies, 14: 383:The main objective of sequencing 868:10.1111/j.1365-2583.2006.00632.x 598:Previous studies indicated that 491:identify their colony partners. 329:Zootermopsis nevadensis nuttingi 154: 23: 768:(Isoptera: Archotermopsidae)". 34:needs additional citations for 526:Reproductive division of labor 1: 583:. The reproductive status in 568:Caste differentiation scheme 347:The Nevada termite lives in 1116: 854:(Isoptera, Termopsidae)". 790:10.1016/j.ibmb.2015.07.013 463:ionotropic receptors (IRs) 454:are similarly expanded in 399:This termite only has two 1100:Insects described in 1858 829:10.1007/s00265-009-0807-5 600:cytochromes P450 (CYP450) 574:histone-modifying enzymes 469:and they are expanded in 437:olfactive receptors (ORs) 331:that has been sequenced. 300:(Isoptera) in the family 266: 259: 151:Scientific classification 149: 141: 132: 125: 58:"Zootermopsis nevadensis" 1095:Insects of North America 856:Insect Molecular Biology 452:gustative receptor (GRs) 447:there are only 63 genes. 908:Zootermopsis nevadensis 852:Hodotermopsis sjostedti 813:Zootermopsis nevadensis 766:Zootermopsis nevadensis 467:Drosophila melanogaster 428:Zootermopsis nevadensis 385:Zootermopsis nevadensis 317:Zootermopsis nevadensis 285:Zootermopsis nevadensis 270:Zootermopsis nevadensis 127:Zootermopsis nevadensis 581:cuticular hydrocarbons 569: 556:development stage. In 327:. It is the genome of 713:Nature Communications 657:Nature Communications 567: 536:Vitellogenines (Vgs) 43:improve this article 782:2015IBMB...64...25M 725:2014NatCo...5.3636T 669:2014NatCo...5.3636T 473:too with 137 genes. 359:, and rural areas. 733:10.1038/ncomms4636 678:10.1038/ncomms4636 570: 252:Z. nevadensis 16:Species of termite 1077: 1076: 1062:Open Tree of Life 900:Taxon identifiers 823:(12): 1799–1807. 551:Juvenile hormones 281: 280: 119: 118: 111: 93: 1107: 1070: 1069: 1057: 1056: 1044: 1043: 1031: 1030: 1018: 1017: 1005: 1004: 992: 991: 979: 978: 966: 965: 953: 952: 940: 939: 927: 926: 925: 895: 888: 887: 847: 841: 840: 808: 802: 801: 761: 755: 754: 744: 707: 701: 700: 690: 680: 647: 611:Cytochromes P450 441:insect olfaction 321:Z. n. nevadensis 302:Archotermopsidae 272: 228:Archotermopsidae 159: 158: 144:Z. n. nevadensis 137: 123: 114: 107: 103: 100: 94: 92: 51: 27: 19: 1115: 1114: 1110: 1109: 1108: 1106: 1105: 1104: 1080: 1079: 1078: 1073: 1065: 1060: 1052: 1047: 1039: 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nevadensis 485: 484:Z. nevadensis 480: 479:antennal lobe 472: 471:Z. nevadensis 468: 464: 460: 457: 456:Z. nevadensis 453: 449: 446: 445:Z. nevadensis 442: 438: 434: 433: 432: 429: 422: 420: 418: 417:Z. nevadensis 413: 406: 404: 402: 397: 395: 391: 386: 378: 376: 374: 370: 362: 360: 358: 354: 350: 342: 340: 334: 332: 330: 326: 322: 318: 311: 309: 307: 303: 299: 295: 291: 287: 286: 273: 271: 265: 262: 261:Binomial name 258: 254: 253: 248: 245: 244: 241: 240: 236: 233: 232: 229: 226: 223: 222: 219: 216: 213: 212: 209: 206: 203: 202: 199: 196: 193: 192: 189: 186: 183: 182: 179: 176: 173: 172: 169: 166: 163: 162: 157: 152: 148: 145: 140: 136: 131: 128: 124: 121: 113: 110: 102: 91: 88: 84: 81: 77: 74: 70: 67: 63: 60: –  59: 55: 54:Find sources: 48: 44: 38: 37: 32:This article 30: 26: 21: 20: 907: 859: 855: 851: 845: 820: 816: 812: 806: 773: 769: 765: 759: 716: 712: 705: 660: 656: 645: 629: 625: 610: 603: 599: 597: 592: 588: 584: 580: 578: 573: 571: 557: 549: 543: 535: 529: 521: 512: 505: 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298:termite 292:, is a 234:Genus: 204:Order: 198:Insecta 194:Class: 83:scholar 1067:612406 1054:136037 1028:623965 1002:296482 976:ZOOTNE 963:472120 950:162746 937:201671 882:  874:  835:  796:  749:  695:  379:Genome 373:shrews 288:, the 85:  78:  71:  64:  56:  1010:IRMNG 880:S2CID 833:S2CID 553:(JHs) 401:opsin 335:Range 90:JSTOR 76:books 1049:NCBI 1023:ITIS 984:GBIF 971:EPPO 932:BOLD 872:PMID 794:PMID 747:PMID 693:PMID 602:and 461:The 450:The 435:The 394:ants 392:and 323:and 62:news 958:EoL 864:doi 825:doi 815:". 786:doi 737:hdl 729:doi 683:hdl 673:doi 45:by 1086:: 1064:: 1051:: 1038:: 1025:: 1012:: 999:: 986:: 973:: 960:: 947:: 934:: 919:: 878:. 870:. 860:15 858:. 831:. 821:63 819:. 792:. 784:. 774:64 772:. 745:. 735:. 727:. 715:. 691:. 681:. 671:. 659:. 655:. 595:. 511:5 504:6 396:. 371:, 355:, 351:, 886:. 866:: 839:. 827:: 800:. 788:: 780:: 753:. 739:: 731:: 723:: 717:5 699:. 685:: 675:: 667:: 661:5 622:. 112:) 106:( 101:) 97:( 87:· 80:· 73:· 66:· 39:.

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"Zootermopsis nevadensis"
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Scientific classification
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Eukaryota
Animalia
Arthropoda
Insecta
Blattodea
Isoptera
Archotermopsidae
Zootermopsis
Binomial name
eusocial
termite
Archotermopsidae
hemimetabolous
deserts
grasslands
prairies

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