000 | 03417nab|a22003977a|4500 | ||
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001 | 66426 | ||
003 | MX-TxCIM | ||
005 | 20230831212238.0 | ||
008 | 20231s2023||||mx |||p|op||||00||0|eng|d | ||
022 | _a1664-462X (Online) | ||
024 | 8 | _ahttps://doi.org/10.3389/fpls.2023.1226072 | |
040 | _aMX-TxCIM | ||
041 | _aeng | ||
100 | 1 |
_aLedesma, A. _931567 |
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245 | 1 | 0 | _aMolecular characterization of doubled haploid lines derived from different cycles of the Iowa Stiff Stalk Synthetic (BSSS) maize population |
260 |
_bFrontiers Media S.A., _c2023. _aSwitzerland : |
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500 | _aPeer review | ||
500 | _aOpen Access | ||
520 | _aMolecular characterization of a given set of maize germplasm could be useful for understanding the use of the assembled germplasm for further improvement in a breeding program, such as analyzing genetic diversity, selecting a parental line, assigning heterotic groups, creating a core set of germplasm and/or performing association analysis for traits of interest. In this study, we used single nucleotide polymorphism (SNP) markers to assess the genetic variability in a set of doubled haploid (DH) lines derived from the unselected Iowa Stiff Stalk Synthetic (BSSS) maize population, denoted as C0 (BSSS(R)C0), the seventeenth cycle of reciprocal recurrent selection in BSSS (BSSS(R)C17), denoted as C17 and the cross between BSSS(R)C0 and BSSS(R)C17 denoted as C0/C17. With the aim to explore if we have potentially lost diversity from C0 to C17 derived DH lines and observe whether useful genetic variation in C0 was left behind during the selection process since C0 could be a reservoir of genetic diversity that could be untapped using DH technology. Additionally, we quantify the contribution of the BSSS progenitors in each set of DH lines. The molecular characterization analysis confirmed the apparent separation and the loss of genetic variability from C0 to C17 through the recurrent selection process. Which was observed by the degree of differentiation between the C0_DHL versus C17_DHL groups by Wright’s F-statistics (FST). Similarly for the population structure based on principal component analysis (PCA) revealed a clear separation among groups of DH lines. Some of the progenitors had a higher genetic contribution in C0 compared with C0/C17 and C17 derived DH lines. Although genetic drift can explain most of the genetic structure genome-wide, phenotypic data provide evidence that selection has altered favorable allele frequencies in the BSSS maize population through the reciprocal recurrent selection program. | ||
546 | _aText in English | ||
650 | 7 |
_aGenetic diversity (as resource) _2AGROVOC _92974 |
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650 | 7 |
_aGenetic resources _2AGROVOC _91127 |
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650 | 7 |
_aZea mays _2AGROVOC _91314 |
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650 | 7 |
_aGenotyping _2AGROVOC _922057 |
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650 | 7 |
_aDoubled haploids _2AGROVOC _929363 |
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650 | 7 |
_aSingle nucleotide polymorphisms _2AGROVOC _910805 |
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700 | 1 |
_aSales Ribeiro, F.A. _931568 |
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700 | 1 |
_aUberti, A. _931569 |
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700 |
_aEdwards, J. _910135 |
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700 | 1 |
_aHearne, S. _8INT3287 _9912 _gGenetic Resources Program |
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700 | 1 |
_aFrei, U.K. _914407 |
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700 | 1 |
_aLübberstedt, T. _98785 |
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773 | 0 |
_tFrontiers in Plant Science _gv. 14, art. 1226072 _dSwitzerland : Frontiers Media S.A., 2023. _w56875 _x1664-462X |
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856 | 4 |
_yOpen Access through DSpace _uhttps://hdl.handle.net/10883/22694 |
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942 |
_cJA _n0 _2ddc |
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999 |
_c66426 _d66418 |