{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,2]],"date-time":"2025-11-02T10:37:45Z","timestamp":1762079865536,"version":"build-2065373602"},"reference-count":34,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2007,5,16]],"date-time":"2007-05-16T00:00:00Z","timestamp":1179273600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["resjournals.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Insect Molecular Biology"],"published-print":{"date-parts":[[2007,8]]},"abstract":"Abstract<\/jats:title>\n \n Tango<\/jats:italic>\n is a transposon of the\n Tc1<\/jats:italic>\n family and was originally discovered in the African malaria mosquito,\n Anopheles gambiae.<\/jats:italic>\n Here we report a systematic analysis of the genome sequence of the yellow fever mosquito,\n Aedes aegypti<\/jats:italic>\n , which uncovered three distinct\n Tango<\/jats:italic>\n transposons. We name the only\n An.\u00a0gambiae Tango<\/jats:italic>\n transposon\n AgTango1<\/jats:italic>\n and the three\n Ae.\u00a0aegypti Tango<\/jats:italic>\n elements\n AeTango1\u20133<\/jats:italic>\n . Like\n AgTango1<\/jats:italic>\n ,\n AeTango1<\/jats:italic>\n and\n AeTango2<\/jats:italic>\n elements both have members that retain characteristics of autonomous elements such as intact open reading frames and terminal inverted repeats (TIRs).\n AeTango3<\/jats:italic>\n is a degenerate transposon with no full\u2010length members. All full\u2010length\n Tango<\/jats:italic>\n transposons contain subterminal direct repeats within their TIRs.\n AgTango1<\/jats:italic>\n and\n AeTango1\u20133<\/jats:italic>\n form a single clade among other\n Tc1<\/jats:italic>\n transposons. Within this clade,\n AgTango1<\/jats:italic>\n and\n AeTango1<\/jats:italic>\n are closely related and share approximately 80% identity at the amino acid level, which exceeds the level of similarity of the majority of host genes in the two species. A survey of\n Tango<\/jats:italic>\n in other mosquito species was carried out using degenerate PCR.\n Tango<\/jats:italic>\n was isolated and sequenced in all members of the\n An.\u00a0gambiae<\/jats:italic>\n species complex,\n Aedes albopictus<\/jats:italic>\n and\n Ochlerotatus atropalpus<\/jats:italic>\n .\n Oc.\u00a0atropalpus<\/jats:italic>\n contains a rich diversity of\n Tango<\/jats:italic>\n elements, while\n Tango<\/jats:italic>\n elements in\n Ae.\u00a0albopictus<\/jats:italic>\n and the\n An.\u00a0gambiae<\/jats:italic>\n species complex all belong to\n Tango1<\/jats:italic>\n . No\n Tango<\/jats:italic>\n was detected in\n Culex pipiens quinquefasciatus<\/jats:italic>\n ,\n Anopheles stephensi, Anopheles dirus<\/jats:italic>\n ,\n Anopheles farauti<\/jats:italic>\n or\n Anopheles albimanus<\/jats:italic>\n using degenerate PCR. Bioinformatic searches of the\n Cx.\u00a0p.\u00a0quinquefasciatus<\/jats:italic>\n (~10\u00a0\u00d7 coverage) and\n An.\u00a0stephensi<\/jats:italic>\n (0.33\u00a0\u00d7 coverage) databases also failed to uncover any\n Tango<\/jats:italic>\n elements. Although other evolutionary scenarios cannot be ruled out, there are indications that\n Tango1<\/jats:italic>\n underwent horizontal transfer among divergent mosquito species.\n <\/jats:p>","DOI":"10.1111\/j.1365-2583.2007.00735.x","type":"journal-article","created":{"date-parts":[[2007,5,16]],"date-time":"2007-05-16T09:54:07Z","timestamp":1179309247000},"page":"411-421","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":5,"title":["Genomic and evolutionary analyses of\n Tango<\/i>\n transposons in\n Aedes aegypti<\/i>\n ,\n Anopheles gambiae<\/i>\n and other mosquito species"],"prefix":"10.1111","volume":"16","author":[{"given":"M. R.","family":"Coy","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Z.","family":"Tu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2007,5,16]]},"reference":[{"key":"e_1_2_7_2_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ympev.2004.11.026"},{"key":"e_1_2_7_3_1","doi-asserted-by":"publisher","DOI":"10.1093\/nar\/25.17.3389"},{"key":"e_1_2_7_4_1","doi-asserted-by":"publisher","DOI":"10.1023\/A:1004185024017"},{"key":"e_1_2_7_5_1","doi-asserted-by":"publisher","DOI":"10.1093\/molbev\/msg189"},{"key":"e_1_2_7_6_1","doi-asserted-by":"crossref","first-page":"335","DOI":"10.1093\/genetics\/133.2.335","article-title":"Bari\u20101, a new transposon\u2010like family in Drosophila melanogaster\n\t\t\t\t\t\twith a unique heterochromatic organization","volume":"133","author":"Caizzi 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