水稻突变体M-20的耐盐生理特性

不同盐（NaCl）浓度的水培条件下,水稻耐盐突变体M－20幼苗生长及生存能力优于其原始品系77－170,膜透性测定表明盐胁迫对M－20质膜的损伤较小;同时,外界盐浓度小于100mmol／L时,M－20幼苗根、地上部的钠离子含量低于其原始品系。土培幼苗浇灌盐水（10mmol／L）时,M－20成熟及生长叶片的内源ABA水平增加时期晚于原始品系,增幅也小;而游离脯氨酸的增加时期虽晚,但增幅远高于原始品系。     

灌溉施肥水平对盐渍化农田水盐分布及玉米产量的影响

水资源缺乏和过量施肥影响着干旱半干旱盐渍化地区农业的发展.研究不同灌溉和施肥量对土壤水盐分布和青贮玉米产量的影响,可为该区确定适宜的灌溉和施肥量提供依据.试验于2015和2016年在大同盆地的盐渍化农田进行,设3种灌溉水平:土壤水分上限分别为田间持水率(θ_f)的100%(W₁)、90%(W₂)和80%(W₃),根据各处理灌溉前的土壤平均实际含水率计算灌水量;2015年设4种施肥水平:900(F₁)、750(F₂)、600(F₃)和450 kg·hm^-2(F₄),2016年设F₁、F₂和F₃共3种.试验用化肥为缓释复合肥,总养分含量48%,其中N:P₂O₅:K₂O的比例为30:12:6.结果表明: 土壤表层电导率随施肥量的增加而增大,施肥水平对平均电导率(EC)和含水率的影响在0～10 cm土层显著,与F₁相比,F₂的0～10 cm土层平均EC在2015年和2016年分别降低25.6%～42.7%和6.4%～7.7%.20～80 cm土层的水分含量随施肥量的增加而降低,与F₁相比,2015年F₂、F₃和F₄处理20～80 cm土层平均土壤含水率分别增加5.9%、16.7%和16.7%,2016年F₂和F₃分别增加13.3%和16.7%.产量在两年中均表现为F₁和F₂高于F₃和F₄,W₃低于W₁和W₂; F₁和F₂的产量差异不明显;与W₁相比,W₂的产量减少低于15 %.因此,施复合肥600～750 kg·hm^-2(氮肥含量180～270 kg·hm^-2),且灌溉水平为W₁和W₂时,可以保证该地区盐渍化土壤种植玉米获得较高的产量,并且不会造成根系层的盐分积累.     

Molecular Biological Identification of a Rice Salt Tolerant Line

A rice salt tolerant line No.170 was obtained from EMS treated anther culture of japonica variety and selected under salinity stress. The salt tolerance trait has been stably inherited through nine generations. In order to characterize this mutant line in molecular biological respects, 130 RFLP genetic markers along 12 pairs of chromosomes based on McCouch’s. rice RFLP linkage map were used to assay polymorphism between the mutant line and its original variety, was shown that allelic differences were found at two linked loci RG711 and RG4 on chromosome 7. Besides, proteins of roots and leaves between the mutant and the control plants were compared by means of two dimensional polyacrylamide gel electrophoresis. The comparison showed that some new proteins appeared in the salt tolerant plant under salinity-stress condition, which might be produced by salt inducible genes.     

Dominant Gene cplsr1 Corresponding to Premature Leaf Senescence Resistance in Cotton (Gossypium hirsutum L.)

Cotton (Gossypium hirsutum L.) premature leaf senescence-resistant inbred XLZ33 and senescencesusceptible inbred lines XLZ13 were selected and crossed to produce F1,F1-reciprocal,F2 and BC1 generations...     

水稻核不育系4个柱头性状的遗传分析

为改良水稻(Oryza sativa)核不育系柱头性状提供遗传信息, 调查了粳型核不育系7001S、籼型核不育系Z913S及其杂交、自交获得的F₁、F₂和F_2:3群体的4个柱头性状, 分析了4个性状间的相关性, 并利用主基因+多基因遗传模型对2个世代4个性状进行遗传分析。结果表明, 4个性状两两间呈极显著正相关, 相关系数介于0.274-0.897之间。除F_2:3群体中花柱长度和柱头外露率分别表现出受2对加性-显性主基因和1对负等效加性-显性主基因+多基因控制外, F₂和F_2:3群体的柱头长度、花柱长度、柱头-花柱总长度以及柱头外露率均表现出受2对主基因和多基因控制, 且F_2:3群体中控制花柱长度的主基因表现出加性-显性效应, 其余均表现出加性-显性-上位性效应。2个世代中4个性状均以主基因遗传为主。     

The F1-ATPase beta-subunit is the putative enterostatin receptor

It has been suggested that the F₁-ATPase β-subunit is the enterostatin receptor. We investigated the binding activity of the purified protein with a labeled antagonist, β-casomorphin_1–7, in the absence and presence of cold enterostatin. ¹²⁵I-β-casomorphin_1–7 weakly binds to the rat F₁-ATPase β-subunit. Binding was promoted by low concentrations of cold enterostatin but displaced by higher concentrations. To study the relationship between binding activity and feeding behavior, we examined the ability of a number of enterostatin analogs to affect β-casomorphin_1–7 binding to the F₁-ATPase β-subunit. Peptides that suppressed food intake promoted β-casomorphin_1–7 binding whereas peptides that stimulated food intake or did not affect the food intake displaced β-casomorphin_1–7 binding. Surface plasmon resonance measurements show that the β-subunit of F₁-ATPase binds immobilized enterostatin with a dissociation constant of 150 nM, where no binding could be detected for the assembled F₁-ATPase complex. Western blot analysis showed the F₁-ATPase β-subunit was present on plasma and mitochondrial membranes of rat liver and amygdala. The data provides evidence that the F₁-ATPase β-subunit is the enterostatin receptor and suggests that enterostatin and β-casomorphin_1–7 bind to distinct sites on the protein.     

盐胁迫下根瘤共生豌豆植株对外源钙的生理响应

为明确外源钙对根瘤共生豌豆植株耐盐性的影响机制,本试验采用盆栽方式研究了NaCl (170 mmol·L^-1)胁迫下,外源施加CaCl₂(0、5、15 mmol·L^-1)对接种根瘤菌(菌株15657、15735、Ca66)的两种耐盐性不同品种豌豆(定豌8号、陇豌6号)植株生理指标的影响。结果表明: 接种根瘤菌、施加CaCl₂或接种根瘤菌后施加CaCl₂均提高了豌豆植株的生物量、超氧化物歧化酶(SOD)和过氧化物酶(POD)活性、脯氨酸(Pro)和可溶性糖(SS)含量,降低了丙二醛(MDA)含量;接种根瘤菌后施加15 mmol·L^-1 CaCl₂显著提高了豌豆植株的生物量、POD活性和Pro含量。接种与豌豆植株匹配性较好的15735菌株并施加CaCl₂对豌豆在盐胁迫下各指标的影响相对较小,接种匹配性差的菌株(156567、Ca66)并施加CaCl₂影响较大。经隶属函数综合分析表明,接种根瘤菌后施加CaCl₂的豌豆植株表现出较强的耐盐性,接种15735菌后施加15 mmol·L^-1 CaCl₂的定豌8号隶属函数值为0.814,耐盐性最强。本研究表明,相比接种根瘤菌和施加CaCl₂处理,接种根瘤菌后施加CaCl₂可更有效地提高盐胁迫下豌豆植株的抗氧化酶活性,增强渗透调节能力,降低膜脂过氧化伤害,从而提高豌豆植株的耐盐性。     

Metal–salt co-tolerance and metal removal by indigenous cyanobacterial strains

Chromium and salt tolerance in five indigenous cyanobacterial strains isolated from contaminated sites was investigated along with their metal bioaccumulative potential. All the five species showed significantly better growth when the medium was spiked with salt or chromium. As compared to single metal or salt treatment, the binary metal–salt (MS) treatments had more favorable effect on cyanobacterial growth as indicated by significantly higher concentration of the primary photosynthetic pigment chlorophyll at M₂₀S₂₀₀₀ (9.9–25.3 μg/mL) as compared to that at M₀S₀ (4.0–12.3 μg/mL). Similarly biomass was much higher at M₂₀S₁₀₀₀ and M₂₀S₂₀₀₀ (41.8–86.2 mg/10 mL) as compared to that at control, M₀S₀ (21.5–36.3 mg/10 mL). Accessory pigments like carotenoids and phycobilinproteins too tended to increase significantly in response to both metal and salts in the two species of Lyngbya (L. putealis and L. ceylanica var. constricta) and Gloeocapsa. These species also showed greater potential of chromium bioaccumulation, which increased further as both salt and metal concentration increased. In the two species of Nostoc however, bioaccumulative potential improve at higher metal concentration, but not affected significantly by salt concentration.     

过表达OsCatC基因水稻的获得及其耐盐性机理分析

过氧化氢酶C(Catalase C,CatC)作为重要的抗氧化酶,在水稻发育和胁迫响应方面起重要作用。为了探究CatC在盐胁迫响应中的功能及其作用机制,该研究构建了OsCatC过表达转基因水稻,并比较了其耐盐性和相关抗逆生理指标的变化。结果表明:(1)成功构建过量表达载体pCUbi1390-OsCatC-Flag,并经农杆菌介导的愈伤组织转化获得了30个独立转基因株系(T0),Western blot鉴定T1代幼苗共获得2个OsCatC过表达株系(OE-10、OE-18);qRT-PCR分析发现,OE-10和OE-18株系的OsCatC转录水平显著高于野生型(WT),证明OsCatC基因已成功过表达于转基因株系(OE-10、OE-18)中,且能正常翻译为融合蛋白CatC-Flag。(2)正常水培条件下,OE-10和OE-18与WT的水稻幼苗长势无明显差异,200 mmol·L-1 NaCl处理7 d后再恢复水培10 d时,OE-10和OE-18幼苗的存活率为20%~25%,而WT幼苗绝大部分则干枯死亡,存活率仅为5%左右。(3)与WT相比,OsCatC过表达水稻(OE-10和OE-18)幼苗的耐盐性显著增强,其盐胁迫下的相对电导率、丙二醛和H₂O₂含量显著降低,过氧化氢酶活性显著升高;4μmol·L^-1甲基紫精(MV)处理7 d后,OE-10和OE-18生长受抑制程度显著小于WT,且幼苗的长度均显著大于WT,表现出较强的氧化胁迫耐受性。研究发现,CatC主要通过降解盐胁迫下过量积累的H₂O₂,减轻氧化损伤,从而提高水稻的耐盐性,证明过表达OsCatC能显著提高水稻对盐胁迫的耐受性,且OsCatC是一个非常好的水稻耐盐候选基因。     

The number and localisation of adenine nucleotide-binding sites in beef-heart mitochondrial ATPase (F1) determined by photolabelling with 8-azido-ATP and 8-azido-ADP

1. When irradiated 8-azido-ATP becomes covalently bound (as the nitreno compound) to beef-heart mitochondrial ATPase (F₁) as the triphosphate, either in the absence or presence of Mg²⁺, label covalently bound is not hydrolysed.

2. In the presence of Mg²⁺ the nitreno-ATP is bound to both the and β subunits, mainly (63%) to the subunits.

3. After successive photolabelling of F₁ with 8-azido-ATP (no Mg²⁺) and 8-azido-ADP (with Mg²⁺) 4 mol label is bound to F₁, 2 mol to the and 2 mol to the β subunits.

4. When the order of photolabelling is reversed, much less 8-nitreno-ATP is bound to F₁ previously labelled with 8-nitreno-ADP. It is concluded that binding to the -subunits hinders binding to the β subunits.

5. F₁ that has been photolabelled with up to 4 mol label still contains 2 mol firmly bound adenine nucleotides per mol F₁.

6. It is concluded that at least 6 sites for adenine nucleotides are present in isolated F₁.     

不同水稻种质在不同生育期耐盐鉴定的差异

以21份水稻(Oryza sativa)种质为材料,用1.5%Na Cl处理种子8天后测定发芽率。在苗期用不同浓度NaCl水培处理10天,测定叶片死亡率等指标和高亲和性K+转运基因(HKT)家族变异。在成株期选3份种质,用不同浓度NaCl盆栽处理,在开花期和籽粒蜡熟期测定植株可溶性糖和生物量等指标,以明确各种质不同生育期的耐盐差异和关键指标。结果表明,在NaCl胁迫下,种子发芽率受到显著影响。苗期盐胁迫后,各种质的平均叶片死亡率变幅最大。在被鉴定的8个耐盐种质中,HKT家族的7个基因除OsHKT2;4外均存在。在≤1 g·kg–1盐胁迫下植株可溶性糖含量表现出刺激增长效应。CG15R单株生物量与盐浓度呈正相关,且随盐浓度的增加而缓慢增长。在≤1 g·kg–1时,中花9号的生物量随盐浓度的增加而增加。水稻耐盐性具有明显的阶段发育特异性,且不同发育阶段的耐盐性之间无相关性。叶片死亡率与蜡熟期生物量可分别作为苗期和成株期耐盐鉴定的关键指标。CG15R可作为高耐盐种质进行深入分析和利用。     

甲氰菊酯和阿维菌素对柑橘全爪螨的亚致死效应

通过叶碟饲养的方法, 利用生命表技术,研究了甲氰菊酯和阿维菌素亚致死剂量LC₂₀处理柑橘全爪螨若螨后,对试验种群当代(F₀)和后代(F₁、F₂代)生长发育及繁殖的影响.结果表明: 甲氰菊酯LC₂₀处理若螨后,当代雌成螨产卵量显著增加;F₁、F₂代的产卵前期缩短,后代雌性比例增大,且均与对照差异显著;同时,F₁和F₂代种群内禀增长率(r_m)和周限增长率(λ)增大,世代历期(T)和种群加倍时间(Dt)缩短,且F₂代与对照相比差异显著.用阿维菌素LC₂₀处理若螨后,当代种群雌成螨产卵量显著下降; F₁和F₂代的产卵量也显著下降,但后代雌性比例增大,产卵前期显著缩短;F₁和F₂代的种群r_m和λ增大,T和Dt缩短,且F₂代比F₁代更为明显.总体来看,甲氰菊酯和阿维菌素亚致死浓度LC₂₀对柑橘全爪螨的影响并不完全相同,甲氰菊酯能够促进当代种群的发展,而阿维菌素对当代种群有一定的抑制作用;但两种杀螨剂亚致死浓度处理柑橘全爪螨对后代种群都有一定的促进作用.研究结果对柑橘全爪螨综合防治策略的制定有一定的指导意义.     

Proteins required for the binding of mitochondrial ATPase to the mitochondrial inner membrane

1. Isolated F₁ (mitochondrial ATPase) binds to urea-treated submitochondrial particles suspended in sucrose/Tris/EDTA with a dissociation constant of 0.1 μM.

2. About one-third of the F₁ and the oligomycin-sensitivity conferring protein (OSCP) are lost during preparation of submitochondrial particles prepared at high pH (A particles). None is lost from particles treated with trypsin (T particles).

3. After further treatment with alkali of urea-treated particles, binding of F₁ requires the addition of OSCP. Maximum binding is reached when both OSCP and Fc₂ are added. The concentration of F₁-binding sites in the presence of both OSCP and Fc₂ is about the same as that in TU particles.

4. After further extraction with silicotungstate of urea- and alkali-treated particles, OSCP no longer induces binding of F₁, unless Fc₂ is also present. Fc₂ induces binding in the absence of OSCP but with a lower binding constant and, in contrast to results under all the other conditions studied in this paper, the ATPase activity is oligomycin insensitive.

5. It is tentatively concluded that OSCP is the binding site for F₁ and Fc₂ is the binding site for OSCP.     

The effect of prostaglandin F2β on expiratory flow rates

Prostaglandin F_2β (PGF_2β), a stereoisomer of F₂ was administered by ultrasonic nebulization to eight patients with bronchial asthma and four normal subjects in increasing doses up to a 200 μg maximum dose. Maximum expiratory flow (MEF) and forced vital capacity (FVC) were analyzed at 5, 15, 30, 60 and 120 minutes after administration of aerosol.

All expiratory flow rates were reduced after 5 minutes. Some increase in terminal flow rates was observed after 60 minutes. We conclude that PGF_2β is not an effective bronchodilator at this dose level.     

The Statistical Power of Inclusive Composite Interval Mapping in Detecting Digenic Epistasis Showing Common F2 Segregation Ratios

Epistasis is a commonly observed genetic phenomenon and an important source of variation of complex traits,which could maintain additive variance and therefore assure the long-term genetic gain in breeding.Inclusive composite interval mapping（ICIM） is able to identify epistatic quantitative trait loci（QTLs） no matter whether the two interacting QTLs have any additive effects.In this article,we conducted a simulation study to evaluate detection power and false discovery rate（FDR） of ICIM epistatic mapping,by considering F₂ and doubled haploid（DH） populations,different F₂ segregation ratios and population sizes.Results indicated that estimations of QTL locations and effects were unbiased,and the detection power of epistatic mapping was largely affected by population size,heritability of epistasis,and the amount and distribution of genetic effects.When the same likelihood of odd（LOD） threshold was used,detection power of QTL was higher in F₂ population than power in DH population;meanwhile FDR in F₂ was also higher than that in DH.The increase of marker density from 10 cM to 5 cM led to similar detection power but higher FDR.In simulated populations,ICIM achieved better mapping results than multiple interval mapping（MIM） in estimation of QTL positions and effect.At the end,we gave epistatic mapping results of ICIM in one actual population in rice（Oryza sativa L.）.     

PD-L1基因敲除小鼠构建及初步表型验证

目的 程序性死亡配体-1(PD-L1)是免疫调节途径的重要因子,是抗肿瘤免疫疗法中重要的靶标之一。利用CRISPR/Cas9技术成功构建PD-L1基因敲除小鼠模型,并初步分析其表型。方法 构建Cas9和sgRNA载体,并转录获得RNA,通过显微注射方式将RNA注射到C57BL/6小鼠受精卵中,经过鉴定获得F₀代阳性小鼠。F₀代小鼠与野生型C57BL/6小鼠交配获得F₁代杂合子小鼠,再通过F₁代小鼠自交获得F₂代纯合子小鼠品系。随后通过Real-Time PCR和流式实验分别检测PD-L1基因在mRNA和蛋白质水平上的表达情况。结果 Real-Time PCR和流式实验检测结果显示与野生型C57小鼠相比,PD-L1纯合子小鼠的PD-L1 mRNA相对表达水平和细胞上的蛋白质表达均有显著性下降,仅测定到本底的信号,证实已成功构建PD-L1基因敲除小鼠品系,为PD-L1体内基因功能研究提供了新的小鼠模型。