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Transcript Profiling of Cold Responsive Genes in Medicago faicata

机译:Medicago FaiCata中冷响应基因的转录物分析

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A cold-induced cDNA library containing 2,016 cDNA clones was constructed using suppression subtractive hybridization (SSH) from cold hardy Medicago sativa L. ssp. faicata (L.) Arcang. A total of 928 plasmids were initially screened using reverse Northern blot analysis, and 523 clones were sequenced. We identified 238 unique gene transcripts (84 repeats and 154 singlets). The EST sequences were deposited into GenBank and annotated. Eight representative clones, which encode a EREBP, phosphoinositide-specific phospholipase C (PLC), FtsH, sucrose phosphate synthase (SPS), sucrose synthase (SS), L-myo-inositol-1-phosphate synthase (MIPS), dehydrin-like protein, and a protein of unknown function, were selected as probes for Northern blot analysis. They were all induced at low temperature. The data indicate that SSH is an effective tool for identification of cold responsive genes and suggest that M. faicata rely on typical stress-inducible molecular mechanisms for cold acclimation.
机译:使用来自冷硬化Medicago Sativa L. SSP的抑制减去杂交(SSH)构建含有2,016个cDNA克隆的冷诱导的cDNA文库。 FAICATA(L.)CARCANG。最初使用逆转Northern印迹分析最初筛选总共928个质粒,并测序523个克隆。我们鉴定了238名独特的基因转录物(84个重复和154个单曲)。将EST序列沉积到Genbank和注释中。八个代表性克隆,其编码eREBP,磷酸阳性磷脂脂脂酶C(PLC),Ftsh,蔗糖磷酸合酶(SPS),蔗糖合酶(SS),L-肌醇 - 1-磷酸合酶(MIPS),脱氢样品选择蛋白质和未知功能的蛋白质作为北方印迹分析的探针。它们都在低温下诱导。数据表明,SSH是用于鉴定冷响应基因的有效工具,并表明M. FaiCata依赖于典型的应力诱导的冷驯化分子机制。

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