Deep gene exchange break among Konosirus punctatus populations across the Northwestern Pacific inferred from AFLP and ISSR markers
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Abstract: The correct understanding of fish population structure plays a positive role in their fishery management. The dotted gizzard shad, Konosirus punctatus, is widely distributed in the coastal waters of the Northwestern Pacific. With the over-exploitation of economically important fishes, its importance is increasingly prominent. To further examine the population genetic structure of K. punctatus across the Northwestern Pacific, the amplified fragment length polymorphism (AFLP) and the inter-simple sequence repeats (ISSRs) were employed to perform genetic variation analysis. The results showed that the combination of polyacrylamide gel electrophoresis and silver staining can effectively detect genetic variation for K. punctatus populations. The average proportions of polymorphic loci were 46.26% and 87.13% for AFLP and ISSR markers, respectively, and the genetic diversity parameters showed no obvious differences among populations. Both AMOVA and pairwise Fst suggested that there was significant genetic differentiation between Chinese and Japanese populations. All samples also clustered into two clades based on the UPGMA tree by two markers, which indicated significant genetic differentiation among populations. Consistent with the previous studies, there are two highly differentiated groups at the nuclear gene level and they were suggested to be treated as two separate genetic management units. The results of the present study could provide the genetic management strategy for this important economic species.
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Key words:
- Konosirus punctatus /
- population genetic differentiation /
- AFLP /
- ISSR
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Table 1. Sample information and genetic diversity information of K. punctatus
Populations ID Date of
collectionn Number
of lociNumber of
polymorphic
lociProportion of
polymorphic
loci/%Nei’s genetic
diversityShannon’s
diversity indexAFLP Aomori AM 2006-05 17 192 62 32.29 0.091 8 0.140 1 Tokyo Bay TB 2007-06 27 196 67 34.18 0.080 1 0.126 8 Nagasaki NG 2007-06 27 191 66 34.55 0.077 1 0.123 1 Qingdao QD 2006-04 17 198 70 35.35 0.079 7 0.128 6 Yellow River
EstuaryYR 2007-04 14 195 62 31.79 0.069 5 0.112 8 Zhoushan ZS 2006-05 14 196 65 33.16 0.091 8 0.141 9 Chengshantou CS 2007-05 19 196 74 37.75 0.089 1 0.142 0 Kongdong Island KI 2007-05 16 195 62 31.79 0.061 7 0.102 4 Daya Bay DB 2006-04 15 182 50 27.47 0.062 6 0.099 7 Total 166 214 99 46.26 ISSR Aomori AM 2006-05 18 168 120 71.42 0.179 1 0.277 Nagasaki NG 2007-06 17 167 126 75.44 0.191 1 0.292 3 Qingdao QD 2006-04 18 168 128 76.19 0.182 3 0.284 Zhoushan ZS 2006-05 17 163 118 72.39 0.182 7 0.280 8 Daya Bay DB 2006-04 18 165 127 76.96 0.184 5 0.287 7 Total 202 176 87.13 Table 2. Polymorphism information of primers based on two markers
AFLP primers E-ACC/
M-CTAE-AGA/
M-CTGE-AGG/
M-CTTE-ACG/
M-CTCE-AGA/
M-CTATotal Number of loci 42 71 39 23 39 214 Polymorphic loci 19 31 17 12 20 99 Proportion of polymorphic loci/% 45.23 43.66 43.59 52.17 51.28 46.26 ISSR primers UBC834 ISSR4 UBC841 ISSR62 Total Number of loci 41 58 62 41 \ 202 Noumber of polymorphic loci 39 54 50 33 \ 176 Proportion of polymorphic loci/% 95.12 93.10 80.65 80.49 \ 87.13 Table 3. Pairwise Fst values (below) and genetic distance (above) among K. punctatus populations by AFLP marker
AM TB NG QD ZS YR KI CS DB AM 0.006 8 0.006 2 0.062 6 0.060 9 0.058 9 0.060 7 0.063 4 0.067 8 TB 0.034 49* 0.001 4 0.067 8 0.069 4 0.068 8 0.068 9 0.070 9 0.074 7 NG 0.032 46* −0.006 05 0.067 1 0.068 9 0.066 3 0.064 9 0.067 2 0.071 1 QD 0.337 90** 0.352 47** 0.361 87** 0.002 9 0.003 6 0.002 8 0.002 6 0.005 5 ZS 0.338 42** 0.362 06** 0.373 36** −0.008 73 0.003 2 0.004 8 0.005 5 0.008 YR 0.333 09** 0.362 11** 0.366 64** −0.001 66 −0.007 83 0.004 1 0.003 0.008 3 KI 0.351 59** 0.371 7** 0.370 26** −0.004 98 0.012 15 0.006 18 0.004 4 0.007 CS 0.351 59** 0.375 12** 0.374 37** −0.005 03 0.019 2* −0.003 76 0.013 26 0.004 8 DB 0.351 59** 0.413 14** 0.415 39** 0.0257 2*0.052 09* 0.0567 4*0.047 01* 0.022 2 Note: * Significant values after Bonferroni correct at 5% (P<0.05); ** significant values after Bonferroni correct at 1% (P<0.01). Table 4. Pairwise Fst value (below) and genetic distance (above) between K. punctatus populations by ISSR marker
AM NG QD ZS DB AM 0.005 6 0.105 6 0.109 6 0.127 9 NG −0.006 8 0.109 0.116 0.129 6 QD 0.284 66* 0.273 59* 0.004 7 0.014 9 ZS 0.291 24* 0.284 81* −0.01 0.015 7 DB 0.323 67* 0.307 88* 0.032 21* 0.034 13* Note: * Significant values after Bonferroni correct at 5% (P<0.05); ** significant values after Bonferroni correct at 1% (P<0.01). Table 5. AMOVA of K. punctatus by AFLP and ISSR markers
Source of variation AFLP ISSR Df Sum of squares Variance components Percentage of variation/% Df Sum of squares Variance components Percentage of variation/% All populations Among groups 1 492.437 5.898 97 36.42 1 368.878 8.188 28 36.42 Among populations within groups 7 88.605 0.139 72 0.86 3 71.015 0.212 04 0.86 Within populations 157 1 594.434 10.155 63 62.71 83 1 654.971 19.939 40 62.71 Total 165 2 175.476 16.194 02 87 2 094.864 28.339 73 Japanese group Among populations 2 29.287 0.175 5 1.63 1 18.024 −0.138 11 −0.68 Within populations 68 718.911 10.572 22 98.37 33 674.490 20.439 10 100.68 Total 70 748.197 10.747 71 34 692.514 20.300 98 Chinese group Among populations 5 59.319 0.128 31 1.29 2 52.991 0.389 91 1.95 Within populations 89 875.523 9.837 34 98.71 50 980.480 19.609 61 Total 94 934.842 9.965 65 52 1 033.472 19.999 52 -
Bian Xiaodong, Wan Ruijing, Shan Xiujuan, et al. 2022. Preliminary analysis on recruitment variation and the exogenous driving factors to early life stages of small pelagic fishes in the Laizhou Bay. Journal of Fishery Sciences of China (in Chinese), 29(3): 446–468 Castoe T A, Poole A W, Gu W J, et al. 2010. Rapid identification of thousands of copperhead snake (Agkistrodon contortrix) microsatellite loci from modest amounts of 454 shotgun genome sequence. Molecular Ecology Resources, 10(2): 341–347, doi: 10.1111/j.1755-0998.2009.02750.x Cheang C C, Tsang L M, Ng W C, et al. 2012. Phylogeography of the cold-water barnacle Chthamalus challengeri in the north-western Pacific: effect of past population expansion and contemporary gene flow. Journal of Biogeography, 39(10): 1819–1835, doi: 10.1111/j.1365-2699.2012.02742.x Choi H C, Han I S, Suh Y S, et al. 2015. Feeding habits of larval Konosirus punctatus from the Nakdong River Estuary, Korea. Korean Journal of Fisheries and Aquatic Sciences, 48(5): 752–759, doi: 10.5657/KFAS.2015.0752 Da Silva L N, Essi L, Welker C A D, et al. 2016. Assessing the genetic diversity and population structure of the endangered Chascolytrum bulbosum (Poaceae, Poeae) using AFLP markers. Biochemical Systematics and Ecology, 68: 236–242, doi: 10.1016/j.bse.2016.07.027 Excoffier L, Lischer H E L. 2010. Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows. Molecular Ecology Resources, 10(3): 564–567, doi: 10.1111/j.1755-0998.2010.02847.x Excoffier L, Smouse P E, Quattro J M. 1992. Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics, 131(2): 479–491, doi: 10.1093/genetics/131.2.479 Ferreira D G, Galindo B A, Frantine-Silva W, et al. 2015. Genetic structure of a Neotropical sedentary fish revealed by AFLP, microsatellite and mtDNA markers: a case study. Conservation Genetics, 16(1): 151–166, doi: 10.1007/s10592-014-0648-2 Fields A T, Feldheim K A, Gelsleichter J, et al. 2016. Population structure and cryptic speciation in bonnethead sharks Sphyrna tiburo in the south‐eastern U. S. A. and Caribbean. Journal of Fish Biology, 89(5): 2219–2233, doi: 10.1111/jfb.13025 Gwak W S, Lee Y D, Nakayama K. 2015. Population structure and sequence divergence in the mitochondrial DNA control region of gizzard shad Konosirus punctatus in Korea and Japan. Ichthyological Research, 62(3): 379–385, doi: 10.1007/s10228-014-0450-7 Grant W S, Bowen B W. 1998. Shallow population histories in deep evolutionary lineages of marine fishes: insights from sardines and anchovies and lessons for conservation. The Journal of Heredity 89, 415–426 Han Zhiqiang, Yanagimoto T, Zhang Yaping, et al. 2012. Phylogeography study of Ammodytes personatus in Northwestern Pacific: Pleistocene isolation, temperature and current conducted secondary contact. PLoS One, 7(5): e37425, doi: 10.1371/journal.pone.0037425 Huyghe F, Kochzius M. 2018. Sea surface currents and geographic isolation shape the genetic population structure of a coral reef fish in the Indian Ocean. PLoS One, 13(3): e0193825, doi: 10.1371/journal.pone.0193825 Kamangar B B, Rostamzadeh J. 2015. Genetic diversity and population genetic structure of Wels (Silurus glanis Linnaeus, 1758) in the northwest of Iran. Environmental Biology of Fishes, 98(8): 1927–1934, doi: 10.1007/s10641-015-0411-7 Kawasaki M, Watanabe Y, Shirafuji N, et al. 2006. Larval Konosirus punctatus (Clupeidae) in a brackish river mouth on the Pacific coast of central Japan. Journal of Fish Biology, 68(5): 1362–1375, doi: 10.1111/j.0022-1112.2006.01018.x Kumar S, Stecher G, Tamura K. 2016. MEGA7: molecular evolutionary genetics analysis version 7.0 for bigger datasets. Molecular Biology and Evolution, 33(7): 1870–1874, doi: 10.1093/molbev/msw054 Kuroda K, Kong L, Kawasaki M, et al. 2002. Long-term fluctuations in the catch data of Konoshiro gizzard shad, Konosirus punctatus, around Japan. Bulletin of the Japanese Society of Fisheries Oceanography, 66(4): 239–246 Li Yuan, Zhang Liyan, Wang Liangming. 2016. Population genetics of Konosirus punctatus in Taiwan Strait. Journal of Applied Oceanography (in Chinese), 35(4): 522–528 Liu Jinxian, Gao Tianxiang, Wu Shifang, et al. 2007. Pleistocene isolation in the Northwestern Pacific marginal seas and limited dispersal in a marine fish, Chelon haematocheilus (Temminck & Schlegel, 1845). Molecular Ecology, 16(2): 275–288, doi: 10.1111/j.1365-294X.2006.03140.x Liu Jinxian, Gao Tianxiang, Yokogawa K, et al. 2006. Differential population structuring and demographic history of two closely related fish species, Japanese sea bass (Lateolabrax japonicus) and spotted sea bass (Lateolabrax maculatus) in Northwestern Pacific. Molecular Phylogenetics and Evolution, 39(3): 799–811., doi: 10.1016/j.ympev.2006.01.009 Liu Jianyong, Lun Zhaorong, Zhang Junbing, et al. 2009. Population genetic structure of striped mullet, Mugil cephalus, along the coast of China, inferred by AFLP fingerprinting. Biochemical Systematics and Ecology, 37(4): 266–274, doi: 10.1016/j.bse.2009.04.010 Liu Bingjian, Zhang kun, Zhang Shufei, et al. 2022. Chromosome-level genome assembly of the dotted gizzard shad (Konosirus punctatus) provides insights into its adaptive evolution. Zoological Research, 43(2): 217–220, doi: 10.24272/j.issn.2095-8137.2021.351 Liu Bingjian, Zhang Kun, Zhu Kehua, et al. 2020. Population genetics of Konosirus punctatus in Chinese coastal watersinferred from two mtDNA genes (COI and Cytb). Frontiers in Marine Science, 7: 534, doi: 10.3389/fmars.2020.00534 Lou Fangrui, Qiu Shengyao, Tang Yongzheng, et al. 2021. Comprehensive phylogeny of Konosirus punctatus (Clupeiformes: Clupeidae) based on transcriptomic data. Bioscience Reports, 41(5): BSR20210455, doi: 10.1042/BSR20210455 Meng Xiangqi, Chen Weidong. 2001. Applications of AFLP and ISSR techniques in detecting genetic diversity in the soybean brown stem rot pathogen Phialophora gregata. Mycological Research, 105(8): 936–940, doi: 10.1016/S0953-7562(08)61949-8 Merril C R, Switzer R C, Van Keuren M L. 1979. Trace polypeptides in cellular extracts and human body fluids detected by two-dimensional electrophoresis and a highly sensitive silver stain. Proceedings of the National Academy of Sciences of the United States of America, 76(9): 4335–4339 Myoung S H, Kim J K. 2014. Genetic diversity and population structure of the gizzard shad, Konosirus punctatus (Clupeidae, Pisces), in Korean waters based on mitochondrial DNA control region sequences. Genes & Genomics, 36(5): 591–598 Nei M, Li W H. 1979. Mathematical model for studying genetic variation in terms of restriction endonucleases. Proceedings of the National Academy of Sciences of the United States of America, 76(10): 5269–5273 Ping Honglin, Yu Fangping, Zhang Tao, et al. 2019. Morphological development and allometric growth pattern of Konosirus punctatus at larvae and juvenile stages. Acta Hydrobiologica Sinica (in Chinese), 43(5): 1021–1033 Ping Honglin, Zhang Tao, Shi Huilai, et al. 2024. Principal component and discriminant analyses of morphological traits of cultured Konosirus punctatus at different stage. Journal of Fisheries of China (in Chinese), 48(3): 133–142 Rice W R. 1989. Analyzing tables of statistical tests. Evolution, 43(1): 223–225, doi: 10.2307/2409177 Sabir J S M, Abo-Aba S, Bafeel S, et al. 2014. Characterization of ten date palm (Phoenix dactylifera L. ) cultivars from Saudi Arabia using AFLP and ISSR markers. Comptes Rendus Biologies, 337(1): 6–18 Sambrock J, Russel D W. 2001. Molecular Cloning: A Laboratory Manual (3rd edition). Shan Lezhou, Ma Jianzhong, Shao Xinbin, et al. 2020a. Study on the technique of artificial propagation and larva nursery of Clupanodon punctatus in Yue Qing Bay. Fisheries Science & Technology Information (in Chinese), 47(3): 130–134 Shan Lezhou, Zhang Lining, Shao Xinbin, et al. 2020b. Artificial breeding and venting operation technology of Clupanodon punctatus. Journal of Aquaculture (in Chinese), 41(11): 56–57 Song Na, Gao Tianxiang, Ying Yiping, et al. 2017. Is the Kuroshio current a strong barrier for the dispersal of the gizzard shad (Konosirus punctatus) in the East China Sea? Marine and Freshwater Research, 68(5): 810–820 Song Na, Jia Ning, Yanagimoto T, et al. 2013. Genetic differentiation of Trachurus japonicus from the Northwestern Pacific based on the mitochondrial DNA control region. Mitochondrial DNA, 24(6): 705–712, doi: 10.3109/19401736.2013.773982 Song Na, Yin Lina, Sun Dianrong, et al. 2019. Fine-scale population structure of Collichtys lucidus populations inferred from microsatellite markers. Journal of Applied Ichthyology, 35(3): 709–718, doi: 10.1111/jai.13902 Tzeng T D, Yeh S Y, Hui C F. 2004. Population structure of the kuruma prawn (Penaeus japonicus) in East Asia inferred from mitochondrial DNA sequences. ICES Journal of Marine Science, 61(6): 913–920, doi: 10.1016/j.icesjms.2004.06.015 Volk D R, Konvalina J D, Floeter S R, et al. 2021. Going against the flow: barriers to gene flow impact patterns of connectivity in cryptic coral reef gobies throughout the western Atlantic. Journal of Biogeography, 48(2): 427–439, doi: 10.1111/jbi.14010 Vos P, Hogers R, Bleeker M, et al. 1995. AFLP: a new technique for DNA fingerprinting. Nucleic Acids Research, 23(21): 4407–4414, doi: 10.1093/nar/23.21.4407 Wang Zhiyong, Jayasankar P, Khoo S K. 2000. AFLP fingerprinting reveals genetic variability in common carp stocks from Indonesia. Asian Fisheries Science, 13(2): 139–147 Whitehead P J P. 1985. FAO Species Catalogue. Vol. 7. Clupeoid Fishes of the World (Suborder Clupeoidei). Part 1: Chirocentridae, Clupeidae and Pristigasteridae. Rome: FAO, 305–379 Yan Shuai, Catanese G, Brown C L, et al. 2015. Phylogeographic study on the chub mackerel (Scomber japonicus) in the Northwestern Pacific indicates the late Pleistocene population isolation. Marine Ecology, 36(3): 753–765, doi: 10.1111/maec.12267 Yang Qiaoli, Gao Tianxiang, Miao Zhenqing. 2011. Differentiation between populations of Japanese grenadier anchovy (Coilia nasus) in Northwestern Pacific based on ISSR markers: implications for biogeography. Biochemical Systematics and Ecology, 39(4-6): 286–296, doi: 10.1016/j.bse.2011.07.019 Yang Taiyou, Guan Jianyi, Chen Hongxi, et al. 2008. Genetic diversity in PAPD and ISSR on Squaliobarbus curriculus in Danjiangkou reservoir. Oceanologia et Limnologia Sinica (in Chinese), 39(2): 157–161 Ying Yiping, Chen Yong, Lin Longshan, et al. 2011. Risks of ignoring fish population spatial structure in fisheries management. Canadian Journal of Fisheries and Aquatic Sciences, 68(12): 2101–2120, doi: 10.1139/f2011-116 Zhang Shiyi. 2001. Fauna Sinica (in Chinese). Beijing: Science Press Zhang Baidong, Li Yulong, Xue Dongxiu, et al. 2020a. Population genomic evidence for high genetic connectivity among populations of small yellow croaker (Larimichthys polyactis) in inshore waters of China. Fisheries Research, 225: 105505, doi: 10.1016/j.fishres.2020.105505 Zhang Kun, Liu Yifan, Yin Xiaolong, et al. 2020b. Characterization of the complete mitochondrial genome of Chinese Konosirus punctatus (Clupeiformes, Clupeidae) and phylogenetic studies of Clupeiformes. Mitochondrial DNA Part B, 5(3): 3371–3373, doi: 10.1080/23802359.2020.1823272 Zhang Yunlei, Sun Xiao, Liu Xiaohui, et al. 2022. Impacts of climate changes on the habitat suitability of spawning ground for Konosirus punctatus in the central and southern Yellow Sea. Journal of Fisheries of China (in Chinese), 46(2): 215–223
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