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61.
B. Fuerst‐Waltl B. Rinnhofer C. Fuerst C. Winckler 《Zeitschrift für Tierzüchtung und Züchtungsbiologie》2010,127(2):113-118
Cross‐sucking and intersucking are considered abnormal behaviours in cattle and constitute a common problem in dairy farming. Cross‐sucking in calves is defined as sucking any body parts of another calf whereas intersucking in heifers and cows is defined as sucking the udder or udder area. The aim of this study was to determine the genetic variability for abnormal sucking behaviour by estimating genetic parameters and examining individual differences between sires with large progeny groups. By means of a questionnaire, cattle breeders in the federal state Lower Austria were requested to identify all currently kept animals which are known of either inter‐ or cross‐sucking (both defined as the same binary trait ‘sucking’ with 0 and 1 referring to the absence and presence of this abnormal behaviour) or allowing sucking (also treated as a binary trait, scored as 1 if an animal was known of allowing herd mates to suck and 0 otherwise). Records of 1222 farms and 13 332 dual purpose Simmental females aged between 21 and 700 days were investigated applying a linear animal model with fixed herd × year × season and random genetic animal effect and a threshold sire model with the herd × year × season effect being treated as random. In total, 8.6% and 4.1% of all calves/heifers were observed sucking and allowing sucking, respectively. Heritabilities of 0.040 ± 0.014 and 0.007 ± 0.006 (linear animal model) and 0.116 ± 0.041 and 0.026 ± 0.024 (threshold model) were found for the traits sucking and allowing sucking, respectively. Breeding values were estimated applying the same models for the trait sucking. Taking all 254 sires into account, the Pearson and Spearman correlation coefficients between breeding values estimated by linear animal and sire threshold model were 0.86 and 0.80. Thus, little difference was observed between the two methods. 相似文献
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为筛选多态性丰富的羊草叶绿体非编码区片段,本研究以9个不同地理位置的羊草居群为材料,通过对12个叶绿体非编码区DNA片段测序及其序列间变异分析试图从中找出有遗传差异的叶绿体DNA(cpDNA)片段,并利用有多态性的cpDNA片段进行遗传多样性分析。结果表明,序列ndhF-rpl32、trnL-trnF、trnC-ycf6、aptI-aptH具有比较丰富的变异,可作为下一步研究野生羊草群体遗传学和谱系地理学较为理想的分子标记。在37个羊草个体4条非编码区片段的合并序列中,共检测到15种单倍型,单倍型多态性(Hd)为0.928,核苷酸多态性(Pi)为0.00101;遗传分化指数(Fst)为0.58884,基因流(Nm)为0.17,基因流较小;中性检验Tajima’s D(-1.08542)和Fu’s Fs(-5.301)均为负值,且差异不显著(P>0.10),推测羊草遵循中性进化理论,可能经历过种群扩张;AMOVA结果显示,65%的分子变异出现在居群间,35%出现在居群内;Mantel检验得到,遗传距离与地理距离具有显著相关性(r=0.449,P<0.05);居群分化值Nst 0.386(0.1865)大于Gst 0.234(0.1506),差异显著(P<0.05),表明羊草居群存在分子谱系地理结构。通过系统发育树分析得到,羊草15个单倍型分为两大分支,H2和H10聚为一支,它们与别的居群个体亲缘关系较远,其余单倍型聚为另一支;单倍型网络图显示,H2和H12、H10和H12亲缘关系较远,与系统发育树分析结果基本一致。本研究为羊草的种质资源保护、谱系地理学研究等工作奠定了基础。 相似文献
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为探讨烯效唑(S3307)在寒地红小豆生长中缓解低温伤害、保护根系的作用,建立红小豆抗冷生产技术体系,达到保产增产的目的,在盆栽条件下,以两个红小豆品种宝清红(耐冷型品种)和天津红(冷敏型品种)为材料,于苗期在人工气候室进行低温(15℃,分别持续1,2,3,4,5d)和叶面喷施20mg·L^-1S3307处理,对红小豆根系抗寒生理指标、产量及不同温度敏感性红小豆品种的S3307响应差异进行测定和分析。结果表明,幼苗期低温导致红小豆根系逆境生理指标发生变化,低温诱导SOD、POD和CAT活性的增强,引起可溶性糖和脯氨酸含量的提高,同时也促使MDA含量上升,最终导致红小豆产量下降。与常温条件相比,喷施清水的宝清红和天津红,低温处理3d时,可溶性糖含量分别提高了59.21%和52.57%;脯氨酸含量分别提高了10.12%和25.39%;SOD、POD和CAT活性分别提高了14.92%和11.01%、5.93%和0.75%、53.33%和13.33%。低温处理5d时,可溶性蛋白含量分别提高了6.27%和3.15%;MDA含量分别显著提高了45.41%和51.08%、产量分别显著下降了19.39%和41.69%。低温条件下,喷施S3307与喷施清水的宝清红和天津红相比较,处理3d时,可溶性糖和脯氨酸含量分别提高了22.01%和0.46%、8.55%和1.40%;SOD活性分别提高了13.45%和24.06%、POD活性分别显著提高了23.60%和15.95%,CAT活性分别提高了4.35%和5.88%。处理5d时,MDA含量分别降低了9.05%和4.37%;产量分别显著提高23.06%和43.88%。综上,S3307通过增加可溶性物质和脯氨酸的含量,提高保护酶活性,降低MDA含量,从而缓解低温伤害,进而降低低温对红小豆造成的产量影响。 相似文献
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凋亡素基因真核表达载体的构建及在人肿瘤细胞中的表达 总被引:2,自引:1,他引:2
为探讨凋亡素对肿瘤的基因治疗效果,构建了凋亡素基因的真核表达载体。将凋亡素基因重组入 pc D N A3 载体,并通过脂质体介导凋亡素在人喉癌、人肺癌细胞系中表达;通过 R T P C R 在转染细胞中检测到了凋亡素的 m R N A,这为应用凋亡素进行肿瘤的基因治疗奠定了基础。 相似文献
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Kanako Muta Takako Miyabe‐Nishiwaki Kenichi Masui Isao Yajima Tomoya Iizuka Akihisa Kaneko Ryohei Nishimura 《Journal of veterinary pharmacology and therapeutics》2021,44(1):18-27
The objectives of this study were (a) to establish a population pharmacokinetic model and (b) to investigate the clinical and physiological effects of a single bolus dose of propofol in common marmosets. In Study 1, pharmacokinetic analysis was performed in six marmosets under sevoflurane anaesthesia. 8 mg/kg of propofol was administrated at a rate of 4 mg kg?1 min?1. Blood samples were collected 2, 5, 15, 30, 60, 90, 120 or 180 min after starting propofol administration. Plasma concentration was measured, and population pharmacokinetic modelling was performed. A two‐compartment model was selected as the final model. The population pharmacokinetic parameters were as follows: V1 = 1.14 L, V2 = 77.6 L, CL1 = 0.00182 L/min, CL2 = 0.0461 L/min. In Study 2, clinical and physiological parameters were assessed and recorded every 2 min after 12 mg/kg of propofol was administrated at a rate of 4 mg kg?1 min?1. Immobilization was sustained for 5 min following propofol administration without apparent bradycardia. While combination of propofol and sevoflurane caused apnoea in Study 1, apnoea was not observed following single administration of propofol in Study 2. These data provide bases for further investigation on intravenous anaesthesia using propofol in common marmosets. 相似文献
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