One-step genome editing of elite crop germplasm during haploid induction.
Journal
Nature biotechnology
ISSN: 1546-1696
Titre abrégé: Nat Biotechnol
Pays: United States
ID NLM: 9604648
Informations de publication
Date de publication:
03 2019
03 2019
Historique:
received:
23
03
2018
accepted:
14
01
2019
entrez:
6
3
2019
pubmed:
6
3
2019
medline:
4
4
2019
Statut:
ppublish
Résumé
Genome editing using CRISPR-Cas9 works efficiently in plant cells
Identifiants
pubmed: 30833776
doi: 10.1038/s41587-019-0038-x
pii: 10.1038/s41587-019-0038-x
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
287-292Références
Bortesi, L. & Fischer, R. The CRISPR/Cas9 system for plant genome editing and beyond. Biotechnol. Adv. 33, 41–52 (2015).
doi: 10.1016/j.biotechadv.2014.12.006
Lowe, K. et al. Morphogenic regulators Baby Boom and Wuschel improve monocot transformation. Plant Cell 28, 1998–2015 (2016).
doi: 10.1105/tpc.16.00124
Laurie, D. A. & Bennett, M. D. The production of haploid wheat plants from wheat × maize crosses. Theor. Appl. Genet. 76, 393–397 (1988).
doi: 10.1007/BF00265339
Coe, E. H. A line of maize with high haploid frequency. Am. Nat. 93, 381–382 (1959).
doi: 10.1086/282098
Kasha, K. J. & Kao, K. N. High frequency haploid production in barley (Hordeum vulgare L.). Nature 225, 874–876 (1970).
doi: 10.1038/225874a0
Burke, L. G. et al. Maternal haploids of Nicotiana tabacum L. from seed. Science 206, 585 (1979).
doi: 10.1126/science.206.4418.585
Ravi, M. & Chan, S. W. L. Haploid plants produced by centromere-mediated genome elimination. Nature 464, 615–618 (2010).
doi: 10.1038/nature08842
Nuccio, M. L., Paul, M., Bate, N. J., Cohn, J. & Culter, S. R. Where are the drought tolerant crops? An assessment of more than two decades of plant biotechnology effort in crop improvement. Plant Sci. 273, 110–119 (2018).
doi: 10.1016/j.plantsci.2018.01.020
Char, S. N. et al. An Agrobacterium-delivered CRISPR/Cas9 system for high-frequency targeted mutagenesis in maize. Plant Biotech. J. 15, 257–268 (2016).
doi: 10.1111/pbi.12611
Woo, J. W. et al. DNA-free genome editing in plants with preassembled CRISPR-Cas9 ribonucleoproteins. Nat. Biotechnol. 33, 1162–1164 (2015).
doi: 10.1038/nbt.3389
Chang, M.-T. & Coe, E. in Molecular Genetics Approaches to Maize Improvement (eds Kriz, A. L. & Larkins, B. A.) 127–142 (Springer, Heidelberg, 2009)
Kelliher, T. et al. MATRILINEAL, a sperm-specific phospholipase, triggers maize haploid induction. Nature 542, 105–109 (2017).
doi: 10.1038/nature20827
Yao et al. OsMATL mutation induces haploid seed formation in indica rice. Nat. Plants 4, 530–533 (2018).
doi: 10.1038/s41477-018-0193-y
Gilles, L. M. et al. Loss of pollen‐specific phospholipase NOT LIKE DAD triggers gynogenesis in maize. EMBO J. 36, 707–717 (2017).
doi: 10.15252/embj.201796603
Liu, C. et al. A 4-bp insertion at ZmPLA1 encoding a putative phospholipase A generates haploid induction in maize. Mol. Plant 10, 520–522 (2017).
doi: 10.1016/j.molp.2017.01.011
Ingham, D. J., Beer, S., Money, S. & Hansen, G. Quantitative real time PCR assay for determining transgene copy number in transformed plants. Biotechniques 31, 132–140 (2001).
doi: 10.2144/01311rr04
Tian, X. et al. Hetero-fertilization together with failed egg–sperm cell fusion supports single fertilization involved in in vivo haploid induction in maize. J. Exp. Bot. 69, 4689–4701 (2018).
doi: 10.1093/jxb/ery177
Zhao, X., Xu, X., Xie, H., Chen, S. & Jin, W. Fertilization and uniparental chromosome elimination during crosses with maize haploid inducers. Plant Physiol. 163, 721–731 (2013).
doi: 10.1104/pp.113.223982
Goday, C. & Esteban, M. R. Chromosome elimination in sciarid flies. Bioessays 23, 242–250 (2001).
doi: 10.1002/1521-1878(200103)23:3<242::AID-BIES1034>3.0.CO;2-P
Whipple, C. J. et al. GRASSY TILLERS1 promotes apical dominance in maize and responds to shade signals in the grasses. Proc. Natl Acad. Sci. USA 108, E506–E512 (2011).
doi: 10.1073/pnas.1102819108
Li, Q. et al. Relationship, evolutionary fate and function of two maize co-orthologs of rice GW2-associated with kernel size and weight. BMC Plant Biol. 10, 143 (2010).
doi: 10.1186/1471-2229-10-143
Komatsuda, T. et al. Six rowed barley originated from a mutation in a homeodomain-leucine zipper I-class homeobox gene. Proc. Natl Acad. Sci. USA 104, 1424–1429 (2007).
doi: 10.1073/pnas.0608580104
Song, X.-J., Huang, W., Shi, M., Zhu, M.-Z. & Lin, H.-X. A QTL for rice grain width and weight encodes a previously unknown RING-type E3 ubiquitin ligase. Nat. Genet. 39, 623–630 (2007).
doi: 10.1038/ng2014
Del Toro-De León, G., García-Aguilar, M. & Gillmor, C. S. Non-equivalent contributions of maternal and paternal genomes to early plant embryogenesis. Nature 514, 624–627 (2014).
doi: 10.1038/nature13620
LeBlanc, C. et al. Increased efficiency of targeted mutagenesis by CRISPR/Cas9 in plants using heat stress. Plant J. 93, 377–386 (2018).
doi: 10.1111/tpj.13782
Kelliher, T. et al. Maternal haploids are preferentially induced by CENH3-tailswap transgenic complementation in maize. Front. Plant Sci. 7, 414 (2016).
doi: 10.3389/fpls.2016.00414
Sanei, M., Pickering, R., Kumke, K., Nasuda, S. & Houben, A. Loss of centromeric histone H3 (CENH3) from centromeres precedes uniparental chromosome elimination in interspecific barley hybrids. Proc. Natl Acad. Sci. USA 108, E498–E505 (2011).
doi: 10.1073/pnas.1103190108
Maheshwari, S. et al. Centromere location in Arabidopsis is unaltered by extreme divergence in CENH3 protein sequence. Gen. Res. 27, 471–478 (2017).
doi: 10.1101/gr.214619.116
Larkin, J. C. et al. Roles of the GLABROUS1 and TRANSPARENT TESTA GLABRA genes in Arabidopsis trichome development. Plant Cell 6, 1065–1076 (1994).
doi: 10.2307/3869885
Mochida, K., Tsujimoto, H. & Sasakuma, T. Confocal analysis of chromosome behavior in wheat × maize zygotes. Genome 47, 199–205 (2004).
doi: 10.1139/g03-123
Kosicki, M., Tomberg, K. & Bradley, A. Repair of double-stranded breaks induced by CRISPR–Cas9 leads to large deletions and complex rearrangements. Nat. Biotech. 36, 765–771 (2018).
doi: 10.1038/nbt.4192
Borg, M. et al. The R2R3 MYB transcription factor DUO1 activates a male germline-specific regulon essential for sperm cell differentiation in Arabidopsis. Plant Cell 23, 534–549 (2011).
doi: 10.1105/tpc.110.081059
Sprunck, S. et al. Egg cell-secreted EC1 triggers sperm cell activation during double fertilization. Science 338, 1093–1097 (2012).
doi: 10.1126/science.1223944
Zhong, H., et al. Advances in Agrobacterium-mediated maize transformation. in Maize. Methods in Molecular Biology Vol. 1676 (ed. Lagrimini L.) 41–59 (Humana, New York, 2018).
Cutler, S., et al. Hypersensitive ABA receptors. US Patent 20160194653 (2016).
Matzk, F. & Mahn, A. Improved techniques for haploid production in wheat using chromosome elimination. Plant Breed. 113, 125–129 (1994).
doi: 10.1111/j.1439-0523.1994.tb00714.x
Clough, S. J. & Bent, A. F. Floral dip: a simplified method for Agrobacterium‐mediated transformation of Arabidopsis thaliana. Plant J. 16, 735–743 (1998).
doi: 10.1046/j.1365-313x.1998.00343.x