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Expression analysis of genes associated with sucrose accumulation and its effect on source-sink relationship in high sucrose accumulating early maturing sugarcane variety

机译:蔗糖积累与蔗糖积累相关基因的表达分析及其对高蔗糖源水槽关系的影响早熟甘蔗品种

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Sucrose synthesis/accumulation in sugarcane depends on the source-sink communication wherein source responds to sink demand for photoassimilate supply. Sucrose in stalk (sink) acts as signal, and sends feedback to restrain further synthesis of sucrose by regulating photosynthetic efficiency of leaves (source). Hence sucrose synthesis/accumulation is controlled by many genes and regulatory sequences including 3 invertases (SAI, CWI, NI), sucrose synthase (SuSy) and sucrose phosphate synthase (SPS). SPS and invertase play key role in enhancing sink strength which ultimately promotes greater sucrose accumulation in the sink tissues. In present study, a significant positive correlation was found between sucrose% of source and sink tissues which was greater in the top (R-2=0.679) than middle (R-2=0.580) and bottom (R-2=0.518) internodes, depicting that sucrose accumulation in the stalk bears a direct relation with sucrose translocation efficiency from source. Results indicated an increased sucrose% with maturity, while reducing sugar content decreased with crop growth. qRT-PCR results exhibited an elevated expression of invertase in immature sink tissues depicting increased sink requirement, which declined with maturity. Similarly, increased PEP carboxylase gene expression as observed supported the fact that higher sink demand results in enhanced photosynthetic rate and thus influences the source activity. SPS was found active at initial stage of cane development indicating its role in sucrose synthesis. Thus by studying expression patterns of the different genes both, in source and sink tissues, a better understanding of the sucrose accumulation pathway in sugarcane is possible, which in turn can help in elucidating ways to enhance sucrose concentration in sink.
机译:甘蔗的蔗糖合成/累积取决于源极汇通信,其中源极响应光谱纤维电源的下沉需求。茎秆(水槽)中的蔗糖充当信号,并通过调节叶片(来源)的光合效率来抑制进一步合成蔗糖的反馈。因此,蔗糖合成/积累由许多基因和调节序列控制,包括3个倒差酶(SAI,CWI,Ni),蔗糖合酶(SASY)和蔗糖磷酸合酶(SPS)。 SPS和逆变酶在提高沉槽强度方面发挥关键作用,这最终促进了水槽组织中更大的蔗糖积累。在本研究中,在顶部(R-2 = 0.679)的源源和水组织之间的源碱和水合物组织之间发现显着的正相关性(R-2 = 0.580)和底部(R-2 = 0.518)的节间,描绘了茎中的蔗糖积聚与来自源的蔗糖易位效率直接关系。结果表明蔗糖%增加了成熟,同时减少糖含量随着作物生长而降低。 QRT-PCR结果表明,在未成熟的沉降需要增加的沉没组织中表现出逆变酶的升高表达,这与成熟度下降。类似地,随着观察到的,增加了PEP羧化酶基因表达,支持更高的水槽需求导致增强的光合速率,从而影响源活动。在甘蔗发展的初始阶段发现SPS活跃,表明其在蔗糖合成中的作用。因此,通过研究不同基因的表达模式,在源和水槽组织中,可以更好地理解甘蔗中的蔗糖积聚途径,这反过来可以有助于阐明含水量的蔗糖浓度的方式。

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