4. Characterization and mapping of multiple shoot1
  H. TAZUKE1), N. SENTOKU2, 3), H. KITANO2), J. -I. ITOH1), M. KUSABA1) and Y. NAGATO1)

1) Graduate School of Agricultural and Life Sciences, University of Tokyo, Tokyo, 113-8657 Japan
2) Bioscience and Biotechnology Center, Nagoya University, Nagoya, 464-8601 Japan
3) Present address: National Institute of Agrobiological Sciences, 2-1-2 Kannondai, Tsukuba, 305-8602 Japan

Primary growth of plant is achieved by two apical meristems: shoot apical meristem (SAM) and root apical meristem. Considering the importance of SAM in plant development, elucidating the mechanisms of SAM establishment and maintenance is of primary importance in understanding plant architecture. We isolated two mutants derived from cv. Taichung 65 (odm87 and odm54 Hong et al., 1995). These two mutants formed multiple shoots in one embryo, and their seedlings were bushy. Because these mutants were allelic, we named them multiple shoot1-1 (mps1-1) and mps1-2, respectively.

The abnormality of these mutants first appeared in embryogenesis. Until 7 days after pollination (DAP), we could not discriminate mps1 embryo from wild-type embryo (data not shown). At 13 DAP, about 25%, embryos developed fewer leaves and lacked root cap suggesting that development of the mps1 embryo was retarded compared to the wild-type embryo (Fig. 1A, B). In the mps1 embryos at this stage, the basal region was abnormally enlarged. In mature embryos, ectopic shoot and/or roots were formed in the basal region (Fig. 1C). In most of mps1 embryos, one ectopic root was formed, resulting in two roots in total. The ectopic shoot was observed in about half of mps1 embryos examined. Ectopic shoot was always underdeveloped. Thus, mps1 could have defect in proper apical-basal patterning at the later stage, causing ectopic differentiation of shoot and root in the basal region.

The mps1 plants were dwarf and bushy (Fig. 1D). The multiple shoot phenotype seemed to be caused by at least two reasons. One is the reduced dormancy of axillary buds: in contrast to the axillary bud of the wild- type first leaf that remained dormant, that of mps1 frequently elongated to become a tiller (Fig. 1E). Another reason is the ectopic formation of shoots. In Fig. 1F, three shoots are outgrowing from one seed. Since the number of shoots in mps1 embryo was never more than two, at least one of the three shoots was thought to be formed after germination. Leaves of mps1 plant were short, and lacked collars, ligules and auricles, and blade- sheath boundary was unclear (Fig. 1G). The blade of the mps1 leaves was underdeveloped. In some cases, the leaves seemed to comprise only sheath. The mps1 plants did not enter the reproductive phase (data not shown). These results show that mps1 has pleiotropic effects on the growth and patterning of leaves, tissue differentiation, adventitious bud formation, and bud dormancy.

To map the MPS1 locus, we crossed MPS1/mps1-1 heterozygous plant with cv. Kasalath, and the F2 population was used for mapping. Linkage analysis using 353 mps1-1 homozygous segregants revealed that MPS1 is located in 53.7-55.4 cM on chromosome 8 (Fig. 2).

Reference
Hong S.-K., T. Aoki, H. Kitano, H. Satoh, and Y. Nagato, 1995. Phenotypic diversity of 188 rice embryo mutants. Dev. Genet. 16: 298-310.

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