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(The) role of MOS7, a nucleoporin88 homolog, in the development of Arabidopsis gametophytes : 애기장대의 배우체 형성에 있어 핵공단백질 MOS7의 기능

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dc.contributor.advisor최연희-
dc.contributor.author박근태-
dc.date.accessioned2017-07-14T00:48:40Z-
dc.date.available2017-07-14T00:48:40Z-
dc.date.issued2015-02-
dc.identifier.other000000024708-
dc.identifier.urihttps://hdl.handle.net/10371/121406-
dc.description학위논문 (박사)-- 서울대학교 대학원 : 생명과학부, 2015. 2. 최연희.-
dc.description.abstractUnlike animals, plants have alternation of generation during reproduction, a diploid sporophytic and a haploid gametophytic generation. Both the female and male gametophytes are created by meiosis followed by subsequent haploid mitoses. For more than a decade, a number of genes have been isolated that are expressed during reproductive stage including gametophyte, zygotic embryo and endosperm development. Nevertheless, the details of how these relevant genes interact in the reproductive stage are still poorly characterized. Therefore, I have studied a molecular regulatory mechanism to the understanding of gametophytic and seed development in Arabidopsis thaliana.
In this study, the mos7-5 mutant was isolated based on an abortion phenotype during reproductive stage. MOS7 (Modifier Of Snc1,7) encodes a nucleoporin88 (Nup88) homolog in Arabidopsis. MOS7/mos7-5 mutant is a recessive loss-of-function mutant and no homozygous mutants were obtained. Megagametogenesis did not proceed beyond the FG2 stage in 48% of the mos7-5 heterozygous mutants. The development of embryo sacs was impaired. Similarly, mitotic defects during microgametogenesis were also observed. The mos7-5 allele is haplo-insufficient in sporocytes, resulting in delayed cell arrest during the mitotic division after meiosis completion. After fertilization, about 14% of the seeds were aborted. These aborting seeds were mos7-5 homozygous which were verified by quantitative PCR.
Yeast two hybrid screen identified dynein light chain type 1 family protein and kinectin-related protein, as MOS7-interacting proteins, which were further confirmed by BiFC analysis in planta. Furthermore, interactions between MOS7 and several nucleoporin known to control spindle dynamics, Rae1 and Nup98, were detected. Microtubule-reporter analysis revealed that MOS7 localize at the mitotic spindle structure during mitosis in proliferating cells. Overall microtubule dynamics including spindle assembly, spindle attachment to the kinetochore and phragmoplast formation were defective in MOS7/mos7-5 heterozygous mutants during gametogenesis. These results demonstrate that MOS7 is required for proper microtubule dynamics through interaction with Rae1 and Nup98a or with dynein light chain and kinectin-related proteins during cell divisions. Conclusions made in the developing both gametogenesis can be extrapolated to somatic cells in that microtubule-organizing spindle and phragmoplast formation is the fundamental basis of plant cell growth. Taken together, MOS7 have a critical role in microtubule organization during mitosis in Arabidopsis thaliana.
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dc.description.tableofcontentsABSTRACT...................................................................ⅰ
CONTENTS...................................................................ⅳ
LIST OF FIGURES........................................................ⅷ
LIST OF TABLES......................................................... xi
ABBREVIATIONS........................................................ xii

1. INTRODUCTION.................................................1
1.1 The mechanism of plant reproduction...........................1
1.1.1 Formation of female gamete.................................2
1.1.2 Formation of male gamete....................................3
1.2 Previous studies for isolation of gametophytic mutants.............................................................................4
1.3 Microtubule organization during gametogenesis...........5
1.4 Nuclear pore proteins in Arabidopsis............................7
1.5 Nucleoporins for a successful mitosis...........................9
1.6 Nup88 homologs in other organisms...........................11
1.7 Purpose of the study.....................................................13
2. MATERIAL AND METHODS............................15
2.1 Plant materials and growth conditions........................15
2.2 Seed-set analysis and whole mount clearing.............15
2.3 Pollen viability analysis................................................16
2.4 Confocal laser scanning microscopic analysis............16
2.5 Recombinant plasmid construction..............................17
2.6 Quantitative real-time RT-PCR.................................18
2.7 GUS and GFP expression and DAPI analysis..............19
2.8 Yeast two hybrid assay................................................20
2.9 BiFC...............................................................................21
2.10 Protein gel blotting analysis.........................................21
3. RESULTS...........................................................26
3.1 Isolation of the mos7-5 mutant showing seed set distortion........................................................................26
3.2 Molecular cloning of the MOS7 gene...........................31
3.3 Phenotypic analysis of ovules in mos7-5 mutant......37
3.4 Phenotypic analysis of pollen in mos7-5 mutant.......43
3.5 MOS7 N-terminal domain is implicated in gametophytic development...........................................47
3.6 MOS7 C-terminal domain is implicated in zygotic development...................................................................51
3.7 The haplo-insufficient mos7-5 allele in MMC and PMC results in delayed phenotypic defects after meiosis during subsequent mitotic divisions...............56
3.8 MOS7 is expressed in various tissues and cells including MMC and PMC...............................................64
3.9 Dynein light chain and kinectin-related protein were identified as binding partners to MOS7 protein..........69
3.10 MOS7 binds to dynein light chain and kinectin-related protein in vivo................................................................72
3.11 MOS7 localizes at the mitotic spindle structure during mitosis............................................................................75
3.12 MOS7 modulates overall microtubule dynamics.........78
3.13 MOS7 also interacts with SAC pathway proteins in Yeast...............................................................................84
4. DISCUSSION......................................................91
4.1 Transmission of Mutant mos7-5 Allele......................92
4.2 MOS7 functions during cell division through Interaction with other proteins........................................................95
4.3 Dual functions of MOS7..............................................102
4.3.1 MOS7 function in interphase............................102
4.3.2 MOS7 function in mitosis..................................102
4.4 MOS7 functions in somatic tissues............................106
5. CONCLUSIONS................................................107
6. ACCESSION NUMBERS.................................108
REFERENCES.............................................................109
ABSTRACT IN KOREAN...........................................126
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dc.formatapplication/pdf-
dc.format.extent3413955 bytes-
dc.format.mediumapplication/pdf-
dc.language.isoen-
dc.publisher서울대학교 대학원-
dc.subjectgametogenesis-
dc.subjectnuclear pore complex-
dc.subjectnucleoporin-
dc.subjectmicrotubule dynamics-
dc.subjectmitosis-
dc.subject.ddc570-
dc.title(The) role of MOS7, a nucleoporin88 homolog, in the development of Arabidopsis gametophytes-
dc.title.alternative애기장대의 배우체 형성에 있어 핵공단백질 MOS7의 기능-
dc.typeThesis-
dc.contributor.AlternativeAuthorGuen Tae Park-
dc.description.degreeDoctor-
dc.citation.pagesxii, 128-
dc.contributor.affiliation자연과학대학 생명과학부-
dc.date.awarded2015-02-
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