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The impact of tandem duplication on gene evolution in Solanaceae species
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作者 huang yi-le ZHANG Ling-kui +3 位作者 ZHANG Kang CHEN Shu-min HU Jian-bin CHENG Feng 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2022年第4期1004-1014,共11页
Whole genome duplication(WGD) and tandem duplication(TD) are important modes of gene amplification and functional innovation, and they are common in plant genome evolution. We analyzed the genomes of three Solanaceae ... Whole genome duplication(WGD) and tandem duplication(TD) are important modes of gene amplification and functional innovation, and they are common in plant genome evolution. We analyzed the genomes of three Solanaceae species(Solanum lycopersicum, Capsicum annuum, and Petunia inflata), which share a common distant ancestor with Vitis vinifera, Theobroma cacao, and Coffea canephora but have undergone an extra whole genome triplication(WGT) event. The analysis was used to investigate the phenomenon of tandem gene evolution with(S. lycopersicum) or without WGT(V. vinifera). Among the tandem gene arrays in these genomes, we found that V. vinifera, which has not experienced the WGT event, retained relatively more and larger tandem duplicated gene(TDG) clusters than the Solanaceae species that experienced the WGT event. Larger TDG clusters tend to be derived from older TD events, so this indicates that continuous TDGs(absolute dosage) accumulated during long-term evolution. In addition, WGD and TD show a significant bias in the functional categories of the genes retained. WGD tends to retain dose-sensitive genes related to biological processes, including DNA-binding and transcription factor activity, while TD tends to retain genes involved in stress resistance. WGD and TD also provide more possibilities for gene functional innovation through gene fusion and fission. The TDG cluster containing the tomato fusarium wilt resistance gene I3 contains 15 genes, and one of these genes, Solyc07g055560, has undergone a fusion event after the duplication events. These data provide evidence that helps explain the new functionalization of TDGs in adapting to environmental changes. 展开更多
关键词 tandem duplication whole genome duplication Solanaceae species gene retention gene fusion
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抗ANXA1自身抗体ELISA检测方法的建立及应用 被引量:1
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作者 黄译乐 胡晓强 +6 位作者 叶敏玲 徐建华 李琳 吴祖培 陈宇宁 何金勇 梁玉瑶 《生物技术》 CAS 2022年第5期565-568,575,共5页
[目的]建立检测抗膜联蛋白A1(Annexin A1,ANXA1)自身抗体的ELISA方法,初步探索其临床应用。[方法]设计ANXA1特异性抗原肽并人工合成,用抗原肽制备可检测ANXA1抗体的ELISA板,通过回归方程的建立、精密度的测定和抗干扰能力的验证,建立检... [目的]建立检测抗膜联蛋白A1(Annexin A1,ANXA1)自身抗体的ELISA方法,初步探索其临床应用。[方法]设计ANXA1特异性抗原肽并人工合成,用抗原肽制备可检测ANXA1抗体的ELISA板,通过回归方程的建立、精密度的测定和抗干扰能力的验证,建立检测ANXA1抗体的ELISA方法。用该法检测临床乳腺癌及健康对照患者血清中的抗ANXA1自身抗体。[结果]该方法在抗体浓度0.025~0.400μg/mL范围内线性良好,R2=0.994,连续5次批内和批间变异系数%均小于10%,对乳糜标本和溶血标本的检测相对误差均小于10%,用于乳腺癌患者抗ANXA1自身抗体的诊断上,实验组抗ANXA1自身抗体表达显著高于对照组,差异具有统计学意义(P<0.05)。[结论]建立了抗ANXA1自身抗体检测的ELISA方法,线性范围0.025~0.400μg/mL,变异系数小于10%,对乳糜标本和溶血标本检测的相对误差小于10%,应用于临床初步显示乳腺癌患者血清中抗ANXA1自身抗体高表达。 展开更多
关键词 ANXA1 自身抗体 ELISA 乳腺癌
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