2019
DOI: 10.1007/s00425-019-03136-z
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Allopolyploidization facilitates gene flow and speciation among corn, Zea perennis and Tripsacum dactyloides

Abstract: Main conclusion Tripsacum dactyloides is closely related to Zea mays since Zea perennis and the MTP tri-species hybrid have four possible reproductive modes. Eastern gamagrass (Tripsacum dactyloides L.) and tetraploid perennial teosinte (Zea perennis) are well known to possess genes conferring resistance against biotic and abiotic stresses as well as adaptation to flood and aluminum toxic soils. However, plant breeders have been hampered to utilize these and other beneficial traits for maize improvement due to… Show more

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Cited by 18 publications
(25 citation statements)
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References 50 publications
(52 reference statements)
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“…Second, an allotetraploid (maize-Tripsacum) was generated from crossing tetraploid maize with tetraploid Tripsacum dactyloides via an n + n mating and embryo rescuing. Next, MTP, which has 74 chromosomes with two missing Tripsacum chromosomes, was created from crossing a maize-Tripsacum plant with the perennial tetraploid teosinte (Z. perennis) by a 2n + n mating (Iqbal et al 2019). Thereafter, among the progeny from MTP under open-pollination conditions (Z. mays or Z. perennis), one clone (Yu6) was outstanding and was approved as a forage crop.…”
Section: Chromosome Preparationmentioning
confidence: 99%
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“…Second, an allotetraploid (maize-Tripsacum) was generated from crossing tetraploid maize with tetraploid Tripsacum dactyloides via an n + n mating and embryo rescuing. Next, MTP, which has 74 chromosomes with two missing Tripsacum chromosomes, was created from crossing a maize-Tripsacum plant with the perennial tetraploid teosinte (Z. perennis) by a 2n + n mating (Iqbal et al 2019). Thereafter, among the progeny from MTP under open-pollination conditions (Z. mays or Z. perennis), one clone (Yu6) was outstanding and was approved as a forage crop.…”
Section: Chromosome Preparationmentioning
confidence: 99%
“…9475) were isolated from young leaves using a modified 2× CTAB method (Fu et al 2015), and then labeled with probes with a DIG-High Prime Kit and a Biotin Nick Translation Kit (Roche, Basel, Switzerland), respectively, according to the manufacturer's instructions. The McGISH technique was performed according to the methods of Iqbal et al (2019). The McGISH images were visualized via a phase video microscope (Olympus BX61, Tokyo, Japan) equipped with a charge-coupled-device camera (700 mm CCD) and via Image Pro Plus 6.0 (Media Cybernetics, Silver Spring, USA).…”
Section: Mcgish Presentationmentioning
confidence: 99%
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