Genomic novelty within a "great speciator" revealed by a high-quality reference genome of the collared kingfisher (Todiramphus chloris collaris).
Genomic novelty within a "great speciator" revealed by a high-quality reference genome of the collared kingfisher (Todiramphus chloris collaris).
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DOI:
10.1093/g3journal/jkac260
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发表时间:
2022-11-04
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影响因子:
--
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--
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Islands are natural laboratories for studying patterns and processes of evolution. Research on island endemic birds has revealed elevated speciation rates and rapid phenotypic evolution in several groups (e.g. white-eyes, Darwin’s finches). However, understanding the evolutionary processes behind these patterns requires an understanding of how genotypes map to novel phenotypes. To date, there are few high-quality reference genomes for species found on islands. Here, we sequence the genome of one of Ernst Mayr’s “great speciators,” the collared kingfisher (Todiramphus chloris collaris). Utilizing high molecular weight DNA and linked-read sequencing technology, we assembled a draft high-quality genome with highly contiguous scaffolds (scaffold N50 = 19 Mb). Based on universal single-copy orthologs, we estimated a gene space completeness of 96.6% for the draft genome assembly. The population demographic history analyses reveal a distinct pattern of contraction and expansion in population size throughout the Pleistocene. Comparative genomic analysis of gene family evolution revealed that species-specific and rapidly expanding gene families in the collared kingfisher (relative to other Coraciiformes) are mainly involved in the ErbB signaling pathway and focal adhesion. Todiramphus kingfishers are a species-rich group that has become a focus of speciation research. This draft genome will be a platform for future taxonomic, phylogeographic, and speciation research in the group. For example, target genes will enable testing of changes in sensory structures associated with changes in vision and taste genes across kingfishers.
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影响因子:
3.3
作者:
Cornetti L;Valente LM;Dunning LT;Quan X;Black RA;Hébert O;Savolainen V
通讯作者:
Savolainen V
影响因子:
64.8
作者:
Feng S;Stiller J;Deng Y;Armstrong J;Fang Q;Reeve AH;Xie D;Chen G;Guo C;Faircloth BC;Petersen B;Wang Z;Zhou Q;Diekhans M;Chen W;Andreu-Sánchez S;Margaryan A;Howard JT;Parent C;Pacheco G;Sinding MS;Puetz L;Cavill E;Ribeiro ÂM;Eckhart L;Fjeldså J;Hosner PA;Brumfield RT;Christidis L;Bertelsen MF;Sicheritz-Ponten T;Tietze DT;Robertson BC;Song G;Borgia G;Claramunt S;Lovette IJ;Cowen SJ;Njoroge P;Dumbacher JP;Ryder OA;Fuchs J;Bunce M;Burt DW;Cracraft J;Meng G;Hackett SJ;Ryan PG;Jønsson KA;Jamieson IG;da Fonseca RR;Braun EL;Houde P;Mirarab S;Suh A;Hansson B;Ponnikas S;Sigeman H;Stervander M;Frandsen PB;van der Zwan H;van der Sluis R;Visser C;Balakrishnan CN;Clark AG;Fitzpatrick JW;Bowman R;Chen N;Cloutier A;Sackton TB;Edwards SV;Foote DJ;Shakya SB;Sheldon FH;Vignal A;Soares AER;Shapiro B;González-Solís J;Ferrer-Obiol J;Rozas J;Riutort M;Tigano A;Friesen V;Dalén L;Urrutia AO;Székely T;Liu Y;Campana MG;Corvelo A;Fleischer RC;Rutherford KM;Gemmell NJ;Dussex N;Mouritsen H;Thiele N;Delmore K;Liedvogel M;Franke A;Hoeppner MP;Krone O;Fudickar AM;Milá B;Ketterson ED;Fidler AE;Friis G;Parody-Merino ÁM;Battley PF;Cox MP;Lima NCB;Prosdocimi F;Parchman TL;Schlinger BA;Loiselle BA;Blake JG;Lim HC;Day LB;Fuxjager MJ;Baldwin MW;Braun MJ;Wirthlin M;Dikow RB;Ryder TB;Camenisch G;Keller LF;DaCosta JM;Hauber ME;Louder MIM;Witt CC;McGuire JA;Mudge J;Megna LC;Carling MD;Wang B;Taylor SA;Del-Rio G;Aleixo A;Vasconcelos ATR;Mello CV;Weir JT;Haussler D;Li Q;Yang H;Wang J;Lei F;Rahbek C;Gilbert MTP;Graves GR;Jarvis ED;Paten B;Zhang G
通讯作者:
Zhang G
影响因子:
2.9
作者:
Eliason, Chad M.;McCullough, Jenna M.;Hackett, Shannon J.
通讯作者:
Hackett, Shannon J.
影响因子:
64.8
作者:
Li, Heng;Durbin, Richard
通讯作者:
Durbin, Richard
影响因子:
3.9
作者:
Kyriazis, Christopher C.;Bates, John M.;Heaney, Lawrence R.
通讯作者:
Heaney, Lawrence R.