Hande Atul S, Katageri Ishwarappa S, Jadhav Mangesh P, Adiger Sateesh, Gamanagatti Savita, Padmalatha Kethireddy Venkata, Dhandapani Gurusamy, Kanakachari Mogilicherla, Kumar Polumetla Ananda, Reddy Vanga Siva
University of Agricultural Sciences, Dharwad, Karnataka, India.
National Research Centre on Plant Biotechnology (NRCPB), IARI, New Delhi, India.
BMC Genomics. 2017 Aug 31;18(1):675. doi: 10.1186/s12864-017-4066-y.
Cotton fibre is a single cell and it is one of the best platforms for unraveling the genes express during various stages of fibre development. There are reports devoted to comparative transcriptome study on fiber cell initiation and elongation in tetraploid cultivated cotton. However, in the present investigation, comparative transcriptome study was made in diploid cultivated cotton using isogenic fuzzy-lintless (Fl) and normal fuzzy linted (FL) lines belong to Gossypium arboreum, diploid species at two stages, 0 and 10 dpa (days post anthesis), using Affymetrix cotton GeneChip genome array.
Scanning electron microscopy (SEM) analysis uncovered the occurrence of few fibre cell initials in the Fl line as compared to many in Normal FL at -2 and 0 dpa. However, at 10 dpa there were no fibre cells found elongated in Fl but many elongated cells were found in FL line. Up-regulation of transcription factors, AP2-EREBP, C2H2, C3H, HB and WRKY was observed at 0 dpa whereas in 10 dpa transcription factors, AP2-EREBP, AUX/IAA, bHLH, C2H2, C3H, HB, MYB, NAC, Orphans, PLATZ and WRKY were found down regulated in Fl line. These transcription factors were mainly involved in metabolic pathways such as phytohormone signaling, energy metabolism of cell, fatty acid metabolism, secondary metabolism and other signaling pathways and are related directly or indirectly in fiber development. Quantitative real-time PCR was performed to check fold up or down-regulation of these genes and transcription factors (TFs) down regulated in mutants as compared to normal at 0 and 10 dpa.
This study elucidates that the up-regulation of transcription factors like AP2-EREBP, C2H2, C3H, HB, WRKY and phytohormone signaling genes at 0 dpa and their down-regulation at the 10 dpa might have constrain the fibre elongation in fuzzy-lintless line. Along with this the down-regulation of genes involved in synthesis of VLCFA chain, transcripts necessary for energy and cell wall metabolism, EXPANSINs, arabinogalactan proteins (AGPs), tubulin might also be the probable reason for reduced growth of fibres in the Fl. Plant receptor-like kinases (RLKs), Leucine Rich Repeats) LRR- family protein and signal transduction coding for mitogen-activated protein kinase (MAPK) cascade, have been engaged in coordination of cell elongation and SCW biosynthesis, down-regulation of these might loss the function leads to reduced fibre growth.
棉纤维是单个细胞,是解析纤维发育各个阶段基因表达的最佳平台之一。有报道致力于四倍体栽培棉纤维细胞起始和伸长的比较转录组研究。然而,在本研究中,利用Affymetrix棉花基因芯片基因组阵列,对二倍体栽培棉中属于亚洲棉(一种二倍体物种)的同基因无绒棉(Fl)和正常有绒棉(FL)品系在开花后0天和10天这两个阶段进行了比较转录组研究。
扫描电子显微镜(SEM)分析发现,在开花后-2天和0天,Fl品系中纤维细胞起始较少,而正常FL品系中有许多。然而,在开花后10天,Fl品系中未发现伸长的纤维细胞,而FL品系中有许多伸长的细胞。在开花后0天观察到转录因子AP2-EREBP、C2H2、C3H、HB和WRKY上调,而在开花后10天,Fl品系中的转录因子AP2-EREBP、AUX/IAA、bHLH、C2H2、C3H、HB、MYB、NAC、孤儿基因、PLATZ和WRKY下调。这些转录因子主要参与植物激素信号传导、细胞能量代谢、脂肪酸代谢、次生代谢等代谢途径以及其他信号通路,直接或间接与纤维发育相关。进行了定量实时PCR,以检测这些基因和在突变体中与正常情况相比在开花后0天和10天下调的转录因子(TFs)的上调或下调倍数。
本研究表明,开花后0天转录因子如AP2-EREBP、C2H2、C3H、HB、WRKY和植物激素信号基因的上调以及它们在开花后10天的下调可能限制了无绒棉品系中纤维的伸长。除此之外,超长链脂肪酸(VLCFA)链合成相关基因、能量和细胞壁代谢所需转录本、扩展蛋白、阿拉伯半乳聚糖蛋白(AGP)、微管蛋白的下调也可能是Fl品系中纤维生长减少的原因。植物类受体激酶(RLK)、富含亮氨酸重复序列(LRR)家族蛋白以及有丝分裂原激活蛋白激酶(MAPK)级联信号转导编码蛋白参与细胞伸长和次生细胞壁(SCW)生物合成的协调,这些蛋白的下调可能导致功能丧失,从而导致纤维生长减少。