Abstract
Key message
Using bulked segregant analysis combined with next-generation sequencing, we delimited the pv-ye gene responsible for the golden pod trait of snap bean cultivar A18-1. Sequence analysis identified Phvul.002G006200 as the candidate gene.
Abstract
The pod is the main edible part of snap beans (Phaseolus vulgaris L.). The commercial use of the pods is mainly affected by their color. Consumers seem to prefer golden pods. The aim of the present study was to identify the gene responsible for the golden pod trait in the snap bean. ‘A18-1’ (a golden bean cultivar) and ‘Renaya’ (a green bean cultivar) were chosen as the experimental materials. Genetic analysis indicated that a single recessive gene, pv-ye, controls the golden pod trait. A candidate region of 4.24 Mb was mapped to chromosome Pv 02 using bulked-segregant analysis coupled with whole-genome sequencing. In this region, linkage analysis in an F2 population localized the pv-ye gene to an interval of 182.9 kb between the simple sequence repeat markers SSR77 and SSR93. This region comprised 16 genes (12 annotated genes from the P. vulgaris database and 4 functionally unknown genes). Combined with transcriptome sequencing results, we identified Phvul.002G006200 as the potential candidate gene for pv-ye. Sequencing of Phvul.002G006200 identified a single-nucleotide polymorphism (SNP) in pv-ye. A pair of primers covering the SNP were designed, and the fragment was sequenced to screen 1086 F2 plants with the ‘A18-1’ phenotype. Our findings showed that among the 1086 mapped individuals, the SNP cosegregated with the ‘A18-1’ phenotype. The findings presented here could form the basis to reveal the molecular mechanism of the golden pod trait in the snap bean.
Similar content being viewed by others
References
Ayala-Castro C, Saini A, Outten FW (2008) Fe-s cluster assembly pathways in bacteria. Microbiol Mol Biol Rev 72:110–125. https://doi.org/10.1128/MMBR.00034-07
Bogora L (1962) Porphyrin synthesis. Methods in enzymology. Academic Press, New York, pp 885–891
Delmas F, Sankaranarayanan S, Srijani D, Ellen W, Céline B, Norbert B, Julian GBN, Peter M, Marcus AS (2013) ABI3 controls embryo degreening through Mendel’s I locus. Proceedings of the Proc Natl Acad Sci USA 110:E3888–E3894. https://doi.org/10.1073/pnas.1308114110
Dong H, Fei GL, Wu CY, Wu FQ, Sun YY, Chen MJ (2013) A rice virescent-yellow leaf mutant reveals new insights into the role and assembly of plastid caseinolytic protease in higher plants. Plant Physiol 162:1867–1880. https://doi.org/10.2307/23598522
Frick G, Su Q, Apel K, Armstrong GA (2003) An Arabidopsis porB porC double mutant lacking light-dependent NADPH: protochlorophyllide oxidoreductases B and C is highly chlorophyll-deficient and developmentally arrested. Plant J 35:141–153. https://doi.org/10.1046/j.1365-313X.2003.01798.x
Fromme P, Melkozernov A, Jordan P, Krauss N (2003) Structure and function of photosystem I: interaction with its soluble electron carriers and external antenna systems. FEBS Lett 555:40–44. https://doi.org/10.1016/S0014-5793(03)01124-4
Fu DQ, Meng LH, Zhu BZ, Zhu HL, Yan HX (2016) Silencing of the SlNAP7 gene influences plastid development and lycopene accumulation in tomato. Sci Rep 6:38664. https://doi.org/10.1038/srep38664
Gaubier P, Wu HJ, Laudie M, Delseny M, Grellet F (1995) A chlorophyll synthetase gene from Arabidopsis thaliana. Mol Genet Genomics 249:58–64. https://doi.org/10.1007/BF00290236
Hiroki T, Akira A, Kentaro Y, Shunichi K, Satoshi N, Chikako M, Aiko U, Hiroe U, Muluneh T, Shohei T, Hideki I, Liliana MC, Sophien K, Ryohei T (2013) QTL-seq: rapid mapping of quantitative trait loci in rice by whole genome resequencing of DNA from two bulked populations. Plant J 74:174–183. https://doi.org/10.1111/tpj.12105
Hjorth E, Hadfi K, Zauner S, Maier UG (2005) Unique genetic compartmentalization of the SUF system in cryptophytes and characterization of a SufD mutant in Arabidopsis thaliana. FEBS Lett 579:1129–1135. https://doi.org/10.1016/j.febslet.2004.12.084
Holm G (1954) Chlorophyll mutation in barley. Acta Agric Scand 4:457–471. https://doi.org/10.1080/00015125409439955
Janneke B, Marinus P (2011) Ancient and essential: the assembly of iron-sulfur clusters in plants. Trends in Plant Sci 16:218–226. https://doi.org/10.1016/j.tplants.2010.12.006
Jung KH, Hur J, Ryu CH, Choi Y, Chung YY, Miyao A, Hirochoka H, An G (2003) Characterization of a rice chlorophyll-deficient mutant using the T-DNA gene-trap system. Plant Cell Physiol 44:463–472. https://doi.org/10.1093/pcp/pcg064
Kosambi DD (1944) The estimation of map distance from recombination values. Ann Hum Genet 12:172–175. https://doi.org/10.1111/j.1469-1809.1943.tb02321.x
Kou X, Zhao Y, Wu C, Jiang B, Zhang Z, Rathbun JR, He Y, Xue Z (2018) SNAC4 and SNAC9 transcription factors show contrasting effects on tomato carotenoids biosynthesis and softening. Postharvest Biol Technol 144:9–19. https://doi.org/10.1016/j.postharvbio.2018.05.008
Kusumi K, Sakata C, Nakamura T, Kawasaki S, Yoshimura A, Iba K (2011) A plastid protein NUS1 is essential for build-up of the genetic system for early chloroplast development under cold stress conditions. Plant J 68:1039–1050. https://doi.org/10.1111/j.1365-313X.2011.04755.x
Li H, Durbin R (2009) Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 25:1754–1760. https://doi.org/10.1093/bioinformatics/btp324
Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, Marth G, Abecasis G, Durbin R (2009) The sequence alignment/map format and SAMtools. Bioinformatics 25:2078–2079. https://doi.org/10.1093/bioinformatics/btp352
Liu C, Li YM, Liu DJ, Yan ZS, Feng GJ, Yang XX (2020) Blocked chlorophyll synthesis leads to the production of golden snap bean pods. Mol Genet Genomics 295:1325–1337. https://doi.org/10.1007/s00438-020-01699-1
Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2 (-Delta Delta C (T)) Method. Methods 25:402–408. https://doi.org/10.1006/meth.2001
Masaya K (2012) Mechanism of Carotenoid Accumulation in Citrus Fruit. J Jpn Soc Hort Sci 81:219–233. https://doi.org/10.2503/jjshs1.81.219
Masuda T (2008) Recent overview of the Mg branch of the tetrapyrrole biosynthesis leading to chlorophylls. Photosynth Res 96:121–143. https://doi.org/10.1007/s11120-008-9291-4
Mochizuki N, Brusslan JA, Larkin R, Nagatani A, Chory J (2001) Arabidopsis genomes uncoupled 5 (GUN5) mutant reveals the involvement of Mg-chelatase H subunit in plastid-to-nucleus signal transduction. Proc Proc Natl Acad Sci USA 98:2053–2058. https://doi.org/10.1073/pnas.98.4.2053
Nagata N, Tanaka R, Satoh S, Tanaka A (2005) Identification of a vinyl reductase gene for chlorophyll synthesis in Arabidopsis thaliana and implications for the evolution of Prochlorococcus species. Plant Cell 17:233–240. https://doi.org/10.1105/tpc.104.027276
Ohmiya A, Hirashima M, Yagi M, Tanase K, Yamamizo C (2014) Identification of genes associated with chlorophyll accumulation in Flower Petals. PLoS ONE 9:e113738. https://doi.org/10.1371/journal.pone.0113738
Ooijen J, Van JW (2006) JoinMap 4, Software for the calculation of genetic linkage maps in experimental populations. Kyazma BV, Wageningen, Netherlands
Rebeiz CA, Smith BB, Mattheis JR (1975) Chloroplast biogenesis: Biosynthesis and accumulation of Mg-protoporphyrin IX monoester and other metalloporphyrins by isolated etioplasts and developing chloroplasts. Arch Biochem Biophys 167:351–365. https://doi.org/10.1016/0003-9861(75)90471-3
Ren G, An K, Liao Y, Zhao X, Cao Y, Zhao H, Ge X, Kuai B (2007) Identification of a novel chloroplast protein AtNYE1 regulating chlorophyll degradation during leaf senescence in Arabidopsis. Plant Physiol 144:1429–1441. https://doi.org/10.1104/pp.107.1001722
Richard AT (1975) Biochemical Spectroscopy, vol 1. Adam Hilger Ltd, London, pp 327–333
Richly E, Leister D (2004) An improved prediction of chloroplast proteins reveals diversities and commonalities in the chloroplast proteomes of Arabidopsis and rice. Gene 329:11–16. https://doi.org/10.1016/j.gene.2004.01.008
Sakuraba Y, Rahman ML, Cho SH, Kim YS, Koh HJ, Yoo SC, Paek NC (2013) The rice faded green leaf locus encodes protochlorophyllide oxidoreductase B and is essential for chlorophyll synthesis under light conditions. Plant J 74:122–133. https://doi.org/10.1111/tpj.12110
Tatsuru M, Naoki F, Naoki O, Takamatsu K et al (2003) Functional analysis of isoforms of NADPH: Protochlorophyllide Oxidoreductase (POR), PORB and PORC, in Arabidopsis thaliana. Plant Cell Physiol 44:963–974. https://doi.org/10.1093/pcp/pcg128
Wang P, Gao J, Wan C, Zhang F, Xu Z, Huang X, Sun X, Deng X (2010a) Divinyl chlorophyll (ide) a can be converted to monovinyl chlorophyll (ide) a by a divinyl reductase in rice. Plant Physiol 153:994–1003. https://doi.org/10.1104/pp.110.158477
Wang K, Li M, Hakon H (2010b) ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res 38:e164–e164. https://doi.org/10.1093/nar/gkq603
Wu Z, Zhang X, He B, Diao L, Wan J, Sheng S, Guo XP, Su S, Wang LF, Jiang L, Wang C, Zhai HQ, Wan LM (2007) A chlorophyll-deficient rice mutant with impaired chlorophyllide esterification in chlorophyll biosynthesis. Plant Physiol 145:29–40. https://doi.org/10.1104/pp.107.100321
Xu XM, Adams S, Chua NH, Mller SG (2005) AtNAP1 represents an atypical sufb protein in arabidopsis plastids. J Biol Chem 280:6648–6654. https://doi.org/10.1074/jbc.M413082200
Yang D, Li S, Li M, Yang X, Wang W, Cao Z, Li W (2012) Physiological characteristics and leaf ultrastructure of a novel chlorophyll-deficient chd6 mutant of vitis venifera cultured in vitro. J Plant Growth Regul 31:124–135. https://doi.org/10.1007/s00344-011-9225-9
Yang YH, Guo M, Li R, Shen L, Wang W, Liu M, Zhu Q, Hu Z, He QW, Xue Y, Tang SZ, Gu MH, Yan CJ (2015) Identification of quantitative trait loci responsible for rice grain protein content using chromosome segment substitution lines and fine mapping of qPC-1 in rice (Oryza sativa L.). Mol Breed 35:130. https://doi.org/10.1080/01421590310001605688
Yaronskaya E, Ziemann V, Walter G, Averina N, Borner T, Grimm B (2003) Metabolic control of the tetrapyrrole biosynthetic pathway for porphyrin distribution in the barley mutant albostrians. Plant J 35:512–522. https://doi.org/10.1046/j.1365-313X.2003.01825.x
Zhang K, Liu Z, Shan X, Li C, Tang X, Chi M, Feng H (2017) Physiological properties and chlorophyll biosynthesis in a Pak-choi (Brassica rapa L. ssp. chinensis) yellow leaf mutant, pylm. Acta Physiol Plant 39:22–31. https://doi.org/10.1007/s11738-016-2321-5
Zhao SL, Hong L, Zhao CL, Qu YH, Yuan EP, Yang LY, Zhang XT, Wang SX, Li Y (2017) Pigment content of colorful fruits of Wenshan Capsicum annuum cultivars in ripening period. Chin Agric Sci Bull 33:47–51. https://doi.org/10.11924/j.issn.1000-6850.casb16070126
Zhou K, Ren Y, Lv J, Wang Y, Liu F, Zhou F, Zhao S, Chen S, Peng C, Zhang X, Guo X, Cheng Z, Wang J, Wu F, Jiang L, Wan J (2013) Young leaf chlorosis 1, a chloroplast-localized gene required for chlorophyll and lutein accumulation during early leaf development in rice. Planta 237:279–292. https://doi.org/10.1007/s00425-012-1756-1
Acknowledgements
The present study was supported financially by the National Natural Science Foundation of China Youth Science Foundation Project (Grant No. 32002031); Heilongjiang Provincial Natural Science Foundation of China (Grant Nos. LH2020C090 and LH2019C058); and the basic scientific research operating expenses of provincial College in Heilongjiang province (Grant Nos. 2020-KYYWF-1027 and 2020-KYYWF-1026).
Author information
Authors and Affiliations
Contributions
XY and CL contributed equally to the study. XY and CL designed and performed most of the experiments and wrote the manuscript. ZY provided guidance to phenotype investigation assays, and YL assisted in genetic analysis. GF and DL revised the manuscript and performed data analysis.
Corresponding authors
Ethics declarations
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Ethical standards
The authors note that this research was performed and reported in accordance with ethical standards of the scientific conduct.
Additional information
Communicated by Istvan Rajcan.
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
Rights and permissions
About this article
Cite this article
Yang, X., Liu, C., Li, Y. et al. Identification and fine genetic mapping of the golden pod gene (pv-ye) from the snap bean (Phaseolus vulgaris L.). Theor Appl Genet 134, 3773–3784 (2021). https://doi.org/10.1007/s00122-021-03928-6
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00122-021-03928-6