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Relevant bibliographies by topics / OsMADS4

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Dissertations / Theses

Academic literature on the topic 'OsMADS4'

Author: Grafiati

Published: 6 September 2023

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Dissertations / Theses on the topic "OsMADS4"

1

Gregis, V. "Analisi comparata del controllo molecolare dell'induzione alla fioritura: ruolo dei geni OsMADS22/OsMADS47 e SVP/AGL24 rispettivamente in riso e Arabidopsis." Doctoral thesis, Università degli Studi di Milano, 2007. http://hdl.handle.net/2434/58412.

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2

Khong, Ngan Giang. "Etude fonctionnelle de facteurs de transcription OsMADS25 et OsMADS26 dans le développement et dans la réponse aux différents stress biotique et abiotique chez le riz." Thesis, Montpellier 2, 2010. http://www.theses.fr/2010MON20120.

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Le riz (Oryza sativa L) est la source principale d'alimentation pour plus de la moitié de la population mondiale (Khush, 2005). La production de riz devrait augmenter de plus de 40% en 2030 pour satisfaire la demande de croissance de la population. Chaque année, environ 25% de la production est perdue à cause des insectes ravageurs, des maladies et des mauvaises herbes (Khus, 2005). Des pertes semblables sont dues aux stress abiotiques comme la sécheresse. L'objectif de mon travail de thèse a consisté à étudier la fonction de deux facteurs de transcription (FT) à boîte MADS OsMADS25 et OsMADS2

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3

Zamzam, Mohamed. "Rice transcription factors OsMADS2 and OsMADS4 regulate floret organ development: Deciphering their gene targets, traits and functions related to their unequal genetic redundancy." Thesis, 2023. https://etd.iisc.ac.in/handle/2005/6185.

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Organs in modern dicot flowers are positioned in concentric rings (whorls). The outermost whorl has green protective sepals, internal to which are showy petals, and the reproductive stamen and carpel whorls. Florets of rice, cereals and grasses evolved certain morphological and functionally distinct features in their non-reproductive organs. Striking among them are the highly modified petal analogs; called lodicules, and the large bract-like outermost organs named palea and lemma. The analogy of these modified rice floret organs to sepals and petals is debated. The two lodicules of rice floret

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4

Lin, Shu-Yu, and 林書宇. "Studies on rice genes involved in early flowering regulated by OsMADS14 and panilce exsertion regulated by OsMADS34." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/77230047457895666724.

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碩士<br>國立中興大學<br>分子生物學研究所<br>105<br>M52048, a T-DNA insertion mutant, shows dwarf, early flowering, node bending and impaired in panicle exsertion and it has been demonstrated to have three flanking genes OsMADS14, OsMADS34 and OsCP7 activated. Transgenic plants, Ubi:OsMADS14, ectopically overexpressing OsMADS14 revealed dwarf and early flowering phenotype, and up-regulated expression of florigen genes Hd3a and RFT1 were observed in the previous study. The first part of this study is to investigate the possible mechanisms that how the expression of Hd3a and RFT1 can be up-regulated by OsMADS14.

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5

Li, Tzu-Yin, and 李咨胤. "Characterization of the T-DNA insertion mutant M52048 and functional study of three activated genes OsMADS34、OsMADS14 and OsCP7." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/gp7a2s.

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碩士<br>國立中興大學<br>分子生物學研究所<br>99<br>A rice T-DNA insertion mutant M0052048 showing extreme early flowering, bending tillers and impairment in panicle exertion was isolated from the Taiwan Rice Insertion Mutant (TRIM) library. This mutant contained a copy of the T-DNA tag inserted in the chromosome number 3 at the 64,867 bp position of OSJBa0032E21 BAC clone where the expression of 048-3 (OsMADS34), 048-4 (OsMADS14) and 048-7 (putative cysteine proteinase, OsCP7) genes were activated by the 35S enhancer located in the T-DNA. The OsMADS14 and OsMADS34 are MADS box-containing transcription factors

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6

Yadav, Shri Ram. "Functions For OsMADS2 And OsMADS1 As Master Regulators Of Gene Expression During Rice Floret Meristem Specification And Organ Development." Thesis, 2009. https://etd.iisc.ac.in/handle/2005/2030.

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Plant reproductive development begins when vegetative shoot apical meristems change their fate to inflorescence meristems which develop floral meristems on the flanks. This process of meristem fate change and organ development involves regulated activation and/or repression of many cell fate determining factors that execute down-stream gene expression cascades. Flowers are formed when floral organs are specified on the floral meristem in four concentric whorls. In the model dicot plant Arabidopsis, the identity and pattern of floral organs is determined by combined actions of MADS-domain conta

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7

Yadav, Shri Ram. "Functions For OsMADS2 And OsMADS1 As Master Regulators Of Gene Expression During Rice Floret Meristem Specification And Organ Development." Thesis, 2009. http://etd.iisc.ernet.in/handle/2005/2030.

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Plant reproductive development begins when vegetative shoot apical meristems change their fate to inflorescence meristems which develop floral meristems on the flanks. This process of meristem fate change and organ development involves regulated activation and/or repression of many cell fate determining factors that execute down-stream gene expression cascades. Flowers are formed when floral organs are specified on the floral meristem in four concentric whorls. In the model dicot plant Arabidopsis, the identity and pattern of floral organs is determined by combined actions of MADS-domain conta

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8

Chen, Ying-Chin, and 陳潁芩. "Functional analysis of rice OsMADS14 and OsCP7 genes." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/69776772634934706215.

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碩士<br>國立中興大學<br>分子生物學研究所<br>103<br>The T-DNA mutant M52048 identified from Taiwan Rice Insertional Mutant (TRIM) library showed dwarf, early flowering, node bending and impaired in panicle exertion. Three flanking genes, OsMADS34, OsMADS14 and OsCP7 (putative cysteine protease 7) were activated in this mutant. Both OsMADS34 and OsMADS14 belong to MADS-box gene family that may participate in regulation of flowering time and the identity of floral organ. OsCP7 is a member of C1A cysteine proteases. In this study, the function of OsMADS14 and OsCP7 were further investigated. Previous study has de

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9

Chen, Chou-Fan, and 陳秋帆. "Functional analysis of rice OsMADS14 in transgenic plants." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/85953912950478779278.

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碩士<br>輔英科技大學<br>生物科技系碩士班<br>100<br>Oncidium is one of the most important orchids used for cut flowers and potted plants in Taiwan. The creation of new cultivars with novel traits is important for Oncidium to enhance the competitiveness of orchid industry. However, traditional breeding processes are limited by the long life cycle and self-incompatibility. The objectives of this study intend to analyze rice AP1-like gene OsMADS14 in Arabidopsis and Oncidium through genetic transformation. In this study, the rice gene OsMADS14 driven by maize ubiqutin promoter was introduced into Arabidopsis and

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10

Chang, Fei-Han, and 張斐涵. "Overexpression of OsMADS34 and OsCP7 affecting panicle development in rice." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/18782266113590810452.

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碩士<br>國立中興大學<br>分子生物學研究所<br>103<br>The T-DNA mutant M52048 identified from Taiwan Rice Insertional Mutant (TRIM) library showed dwarf, early flowering, node bending and impaired in panicle exertion. Three flanking genes, OsMADS34, OsMADS14 and OsCP7 (putative cysteine protease 7) were activated in this mutant. Both OsMADS34 and OsMADS14 belong to MADS-box gene family that may participate in regulation of flowering time and the identity of floral organ. OsCP7 encode a putative cysteine protease, belongs to C1A cysteine protease family, its function remains unknown. In this study the function of

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