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      Novel technologies in doubled haploid line development

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          Summary

          haploid inducer line can be transferred ( DH) technology can not only shorten the breeding process but also increase genetic gain. Haploid induction and subsequent genome doubling are the two main steps required for DH technology. Haploids have been generated through the culture of immature male and female gametophytes, and through inter‐ and intraspecific via chromosome elimination. Here, we focus on haploidization via chromosome elimination, especially the recent advances in centromere‐mediated haploidization. Once haploids have been induced, genome doubling is needed to produce DH lines. This study has proposed a new strategy to improve haploid genome doubling by combing haploids and minichromosome technology. With the progress in haploid induction and genome doubling methods, DH technology can facilitate reverse breeding, cytoplasmic male sterile ( CMS) line production, gene stacking and a variety of other genetic analysis.

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          Most cited references106

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          Marker-assisted selection: an approach for precision plant breeding in the twenty-first century.

          DNA markers have enormous potential to improve the efficiency and precision of conventional plant breeding via marker-assisted selection (MAS). The large number of quantitative trait loci (QTLs) mapping studies for diverse crops species have provided an abundance of DNA marker-trait associations. In this review, we present an overview of the advantages of MAS and its most widely used applications in plant breeding, providing examples from cereal crops. We also consider reasons why MAS has had only a small impact on plant breeding so far and suggest ways in which the potential of MAS can be realized. Finally, we discuss reasons why the greater adoption of MAS in the future is inevitable, although the extent of its use will depend on available resources, especially for orphan crops, and may be delayed in less-developed countries. Achieving a substantial impact on crop improvement by MAS represents the great challenge for agricultural scientists in the next few decades.
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            Epigenetic regulation of centromeric chromatin: old dogs, new tricks?

            The assembly of just a single kinetochore at the centromere of each sister chromatid is essential for accurate chromosome segregation during cell division. Surprisingly, despite their vital function, centromeres show considerable plasticity with respect to their chromosomal locations and activity. The establishment and maintenance of centromeric chromatin, and therefore the location of kinetochores, is epigenetically regulated. The histone H3 variant CENP-A is the key determinant of centromere identity and kinetochore assembly. Recent studies have identified many factors that affect CENP-A localization, but their precise roles in this process are unknown. We build on these advances and on new information about the timing of CENP-A assembly during the cell cycle to propose new models for how centromeric chromatin is established and propagated.
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              Phylogenomics of the nucleosome.

              Histones are best known as the architectural proteins that package the DNA of eukaryotic organisms, forming octameric nucleosome cores that the double helix wraps tightly around. Although histones have traditionally been viewed as slowly evolving scaffold proteins that lack diversification beyond their abundant tail modifications, recent studies have revealed that variant histones have evolved for diverse functions. H2A and H3 variants have diversified to assume roles in epigenetic silencing, gene expression and centromere function. Such diversification of histone variants and 'deviants' contradicts the perception of histones as monotonous members of multigene families that indiscriminately package and compact the genome. How these diverse functions have evolved from ancestral forms can be addressed by applying phylogenetic tools to increasingly abundant sequence data.
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                Author and article information

                Contributors
                thomasl@iastate.edu
                chen368@126.com
                Journal
                Plant Biotechnol J
                Plant Biotechnol. J
                10.1111/(ISSN)1467-7652
                PBI
                Plant Biotechnology Journal
                John Wiley and Sons Inc. (Hoboken )
                1467-7644
                1467-7652
                11 September 2017
                November 2017
                : 15
                : 11 ( doiID: 10.1111/pbi.2017.15.issue-11 )
                : 1361-1370
                Affiliations
                [ 1 ] National Maize Improvement Center of China China Agricultural University Beijing China
                [ 2 ] Department of Agronomy Iowa State University Ames IA USA
                [ 3 ] College of Agronomy Xinjiang Agriculture University Urumqi China
                Author notes
                [*] [* ] Correspondence (Tel +8613020023388; fax +860162732333; email chen368@ 123456126.com )

                and

                (Tel 5152945356; fax 5152945356; email thomasl@ 123456iastate.edu )

                [†]

                These authors contributed equally to the work.

                Article
                PBI12805
                10.1111/pbi.12805
                5633766
                28796421
                0eb1e101-bc1a-482b-a08b-c30bbfd3127b
                © 2017 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 16 May 2017
                : 02 August 2017
                : 04 August 2017
                Page count
                Figures: 3, Tables: 1, Pages: 10, Words: 9662
                Funding
                Funded by: National Key Research and Development Plan
                Award ID: 2016YFD0101200
                Funded by: National Natural Science Foundation of China
                Award ID: 31560392
                Funded by: National Institute of Food and Agriculture
                Award ID: IOW01018
                Award ID: IOW04314
                Funded by: Chinese Postdoctoral Fellowship
                Categories
                Review Article
                Review
                Custom metadata
                2.0
                pbi12805
                November 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.2.1 mode:remove_FC converted:10.10.2017

                Biotechnology
                doubled haploid,haploidization,chromosome elimination,genome doubling,minichromosome
                Biotechnology
                doubled haploid, haploidization, chromosome elimination, genome doubling, minichromosome

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