Mapping of quantitative trait loci underlying a magic trait in ongoing ecological speciation

被引:4
|
作者
Takahashi, Tetsumi [1 ,2 ]
Nagano, Atsushi J. [3 ]
Sota, Teiji [4 ]
机构
[1] Univ Hyogo, Inst Nat & Environm Sci, Sanda, Hyogo 6691546, Japan
[2] Museum Nat & Human Act, Div Nat & Environm Management, Sanda, Hyogo 6691546, Japan
[3] Ryukoku Univ, Fac Agr, Otsu, Shiga 5202194, Japan
[4] Kyoto Univ, Grad Sch Sci, Sakyo Ku, Kyoto 6068502, Japan
关键词
Body size; Cichlid fish; Lake Tanganyika; Polygenic inheritance; Telmatochromis temporalis; LAKE TANGANYIKA; BODY-SIZE; CONSEQUENCES; PRESSURES; EVOLUTION; SELECTION; STACKS; GROWTH; IGF1; FISH;
D O I
10.1186/s12864-021-07908-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background Telmatochromis temporalis is a cichlid fish endemic to Lake Tanganyika. The normal and dwarf morphs of this fish are a clear example of ongoing ecological speciation, and body size plays an important role in this speciation event as a magic trait. However, the genetic basis underlying this trait has not been studied. Results Based on double-digested restriction-site associated DNA (ddRAD) sequencing of a hybrid cross between the morphs that includes F0 male, F0 female, and 206 F2 individuals, we obtained a linkage map consisting of 708 ddRAD markers in 22 linkage groups, which corresponded to the previously reported Oreochromis niloticus chromosomes, and identified one significant and five suggestive quantitative trait loci (QTL) for body size. From the body-size distribution pattern, the significant and three of the five suggestive QTL are possibly associated with genes responsible for the difference in body size between the morphs. Conclusions The QTL analysis presented here suggests that multiple genes, rather than a single gene, control morph-specific body size. The present results provide further insights about the genes underlying the morph specific body size and evolution of the magic trait during ecological speciation.
引用
收藏
页数:9
相关论文
共 50 条
  • [41] Time-related mapping of quantitative trait loci underlying tiller number in rice
    Wu, WR
    Li, WM
    Tang, DZ
    Lu, HR
    Worland, AJ
    GENETICS, 1999, 151 (01) : 297 - 303
  • [42] Genetic Mapping of Quantitative Trait Loci Underlying Flowering Time in Chrysanthemum (Chrysanthemum morifolium)
    Zhang, Fei
    Chen, Sumei
    Jiang, Jiafu
    Guan, Zhiyong
    Fang, Weimin
    Chen, Fadi
    PLOS ONE, 2013, 8 (12):
  • [43] Linkage Disequilibrium mapping of quantitative trait loci: multiple trait analysis.
    Akey, JM
    Jin, L
    Xiong, M
    AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 227 - 227
  • [44] MULTIPLE-TRAIT ANALYSIS OF GENETIC-MAPPING FOR QUANTITATIVE TRAIT LOCI
    JIANG, CJ
    ZENG, ZB
    GENETICS, 1995, 140 (03) : 1111 - 1127
  • [45] Multiple-Interval Mapping for Quantitative Trait Loci With a Spike in the Trait Distribution
    Li, Wenyun
    Chen, Zehua
    GENETICS, 2009, 182 (01) : 337 - 342
  • [46] Mapping Quantitative Trait Loci Underlying Function-Valued Traits Using Functional Principal Component Analysis and Multi-Trait Mapping
    Kwak, Il-Youp
    Moore, Candace R.
    Spalding, Edgar P.
    Broman, Karl W.
    G3-GENES GENOMES GENETICS, 2016, 6 (01): : 79 - 86
  • [47] Mapping Quantitative Trait Loci for Resistance to Rice Blast
    Jia, Y.
    Liu, G.
    PHYTOPATHOLOGY, 2011, 101 (02) : 176 - 181
  • [48] Mapping of quantitative trait loci on porcine chromosome 4
    Walling, GA
    Archibald, AL
    Cattermole, JA
    Downing, AC
    Finlayson, HA
    Nicholson, D
    Visscher, PM
    Walker, CA
    Haley, CS
    ANIMAL GENETICS, 1998, 29 (06) : 415 - 424
  • [49] Mapping Environment-Specific Quantitative Trait Loci
    Chen, Xin
    Zhao, Fuping
    Xu, Shizhong
    GENETICS, 2010, 186 (03) : 1053 - 1066
  • [50] Lineage-specific mapping of quantitative trait loci
    Chen, C.
    Ritland, K.
    HEREDITY, 2013, 111 (02) : 106 - 113