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TAP2 Effect on Min-Pig Stromal Vascular Fraction Cell Gene Expression TAP2 对小型猪基质血管馏分细胞基因表达的影响
IF 0.5 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2024-03-08 DOI: 10.3103/s0095452724010080
Liang Wang, Di Liu, Hong Ma, Dongjie Zhang, Xinmiao He, Wentao Wang, Bo Fu, Zhongqiu Li, Zhenhua Guo

We have hypothesized that the TAP2 gene is associated with lipid metabolism. Here, 10 Min-pig tissues were collected to detect the expression of TAP2 in different tissues. We obtained dorsal subcutaneous structural vascular fraction (SVF) cells from the Min-pig’s back adipose tissue and induced SVF cells into mature adipocytes. By overexpression and interference, the effect of TAP2 on fat deposition in Min-pig SVF cells was studied. Recombinant human insulin, dexamethasone, indomethacin, 3-isobutyl-1-methylxanthine, triiodothyronine, and rosiglitazone could successfully induce SVF cells into mature adipocytes, and the induction efficiency was above 50%. The tissue expression profile showed that TAP2 was expressed in different tissues, and the highest expression was found in back fat, spleen, and back muscle. Overexpression of the TAP2 gene in SVF cells could significantly increase the expression of adipose differentiation-related genes. The expression of TAP2 in SVF cells was reduced to 0.6 times after transfection of the TAP2 gene interference fragment. The adipogenic transcription factor gene C/EBPα, fatty acid synthase gene FSA, and adipocyte directional differentiation factor ADD1 were downregulated, while the expression of lipolysis-related gene LPL was inhibited. In conclusion, TAP2 expression can promote the deposition of subcutaneous fat on Min-pig’s back adipose tissue.

我们推测 TAP2 基因与脂质代谢有关。在此,我们采集了 10 个迷你猪组织,以检测 TAP2 在不同组织中的表达。我们从迷你猪背部脂肪组织中获得背侧皮下结构血管部分(SVF)细胞,并将 SVF 细胞诱导成成熟脂肪细胞。通过过表达和干扰,研究了 TAP2 对迷你猪 SVF 细胞脂肪沉积的影响。重组人胰岛素、地塞米松、吲哚美辛、3-异丁基-1-甲基黄嘌呤、三碘甲状腺原氨酸和罗格列酮能成功诱导SVF细胞转化为成熟脂肪细胞,诱导效率在50%以上。组织表达谱显示,TAP2在不同组织中均有表达,其中以背部脂肪、脾脏和背部肌肉的表达量最高。在 SVF 细胞中过表达 TAP2 基因可显著增加脂肪分化相关基因的表达。转染TAP2基因干扰片段后,TAP2在SVF细胞中的表达量减少到0.6倍。成脂转录因子基因 C/EBPα、脂肪酸合成酶基因 FSA 和脂肪细胞定向分化因子 ADD1 的表达被下调,而脂肪分解相关基因 LPL 的表达受到抑制。总之,TAP2的表达可促进闽猪背部脂肪组织皮下脂肪的沉积。
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引用次数: 0
β-Tubulin of Fusarium as a Potential Target for Realization of Antifungal Activity of Ivermectin 镰刀菌的β-微管蛋白是实现伊维菌素抗真菌活性的潜在靶标
IF 0.5 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2024-03-08 DOI: 10.3103/s009545272401002x
Y. O. Kustovskiy, A. Y. Buziashvili, S. P. Ozheredov, Y. B. Blume, A. I. Yemets

The analysis of the effect of ivermectin on phytopathogenic strains of Fusarium graminearum (F‑55644, F-55748) and Fusarium oxysporum f. sp. lycopersici (F-52897, F-55547) was carried out; as a result, its concentrations were established at which a fungistatic effect on the growth of colonies of the specified strains was observed (2 and 3 mg/mL). It was found that F. oxysporum strains were more susceptible in general to ivermectin than F. graminearum strains. Since it is known that ivermectin is able to interact with β-tubulin (causing a stabilization of microtubules), to explain the obtained results, a 3-dimensional model of the complex of this compound with Fusarium β-tubulin was developed and ivermectin-induced changes in the conformation of β-tubulin were determined, including, particularly, the stabilization and spiralization of the M‑loop of the β-tubulin molecule. This structural element of β-tubulin plays an important role in the lateral contacts between tubulin subunits of adjacent protofilaments within the microtubule. Since the M-loop stabilization reflects a very important feature of microtubule stabilizing agents' binding to the taxane site of β-tubulin, it can be supposed, that ivermectin possesses the same effect on Fusarium microtubules. The results obtained allow for considering ivermectin or its derivatives as potential compounds with fungicidal activity.

分析了伊维菌素对禾谷镰刀菌(F-55644、F-55748)和氧孢镰刀菌(F-52897、F-55547)植物病原菌菌株的影响;结果确定了伊维菌素对特定菌株菌落生长有杀菌作用的浓度(2 和 3 mg/mL)。研究发现,一般来说,草孢霉菌株比禾本科菌株对伊维菌素更敏感。由于已知伊维菌素能与β-微管蛋白相互作用(导致微管稳定化),为了解释所获得的结果,我们建立了该化合物与镰刀菌β-微管蛋白复合物的三维模型,并确定了伊维菌素诱导的β-微管蛋白构象变化,尤其包括β-微管蛋白分子 M 环的稳定化和螺旋化。β-微管蛋白的这一结构元素在微管内相邻原丝的微管蛋白亚基之间的横向联系中起着重要作用。由于 M 环的稳定反映了微管稳定剂与 β-微管蛋白的类固醇位点结合的一个非常重要的特征,因此可以认为伊维菌素对镰刀菌微管也有同样的作用。根据研究结果,可以将伊维菌素或其衍生物视为具有杀菌活性的潜在化合物。
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引用次数: 0
Effect of the Nitrogen Source on the Synthesis of Secondary Metabolites by Suspension Culture of Medicinal Asparagus Asparagus officinalis L. 氮源对药用芦笋悬浮培养次生代谢产物合成的影响
IF 0.5 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2024-03-08 DOI: 10.3103/s0095452724010031
A. O. Skuba, A. F. Likhanov, L. M. Butsenko, Yu. V. Kolomiiets

Medicinal asparagus contains unique compounds that can stop the development of cancerous tumors and even destroy cancer cells. However, there is still insufficient information about the features of the biosynthesis of these compounds and the conditions for their production. In this paper, the influence of an inorganic nitrogen source on the growth of a suspended culture of medicinal asparagus, the accumulation of phenolic compounds in the culture and culture liquid, and the synthesis of saponins is studied. A callus and suspension culture of medicinal asparagus Asparagus officinalis L. were obtained under in vitro conditions. For further research, concentrations of growth regulators 1 mg/L kinetin and 1.5 mg/L 2,4-D were selected. The fastest growth of the suspension culture was established on the medium with a concentration of potassium nitrate of 1900 mg/L and ammonium sulfate of 250 mg/L. Individual explants demonstrated spontaneous differentiation of callus tissue that affected the increase in callus mass and the ratio of the concentration of exophenols to the total mass of the explant. The highest concentrations of endo- and exophenols were obtained on a medium without ammonium nitrogen sources. A positive effect of the medium with a concentration of ammonium sulfate of 500 mg/L on the synthesis of the main steroidal saponins of Asparagus officinalis L. was determined. As a result of the study, a modified MS medium was developed that promotes the accumulation of steroid saponins in a suspension culture of medicinal asparagus.

药用芦笋含有独特的化合物,可以阻止癌症肿瘤的发展,甚至可以消灭癌细胞。然而,有关这些化合物的生物合成特点及其生产条件的信息仍然不足。本文研究了无机氮源对药用芦笋悬浮培养物生长、培养物和培养液中酚类化合物积累以及皂苷合成的影响。在离体条件下获得了药用芦笋 Asparagus officinalis L. 的胼胝体和悬浮培养物。为进一步研究,选择了浓度为 1 毫克/升的生长调节剂木犀草素和 1.5 毫克/升的 2,4-D。在硝酸钾浓度为 1900 毫克/升、硫酸铵浓度为 250 毫克/升的培养基上,悬浮培养物的生长速度最快。单个外植体显示出胼胝组织的自发分化,这影响了胼胝体质量的增加和外酚浓度与外植体总质量的比率。在不含铵态氮源的培养基上获得的内酚和外酚浓度最高。硫酸铵浓度为 500 mg/L 的培养基对芦笋主要甾体皂苷的合成有积极影响。研究结果表明,改良的 MS 培养基可促进药用芦笋悬浮培养基中甾体皂苷的积累。
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引用次数: 0
The Role of Cytogenetic Rearrangements in the Formation of Resistance in Relapse of Acute Lymphoblastic Leukemia 细胞遗传学重排在急性淋巴细胞白血病复发抗药性形成过程中的作用
IF 0.5 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2024-03-08 DOI: 10.3103/s0095452724010067
S. V. Andreieva, K. V. Korets, I. M. Skorokhod, O. M. Tsyapka, I. M. Serbin

Abstract

Cytogenetic rearrangements were studied in bone marrow cells of 24 patients with relapse of acute lymphoblastic leukemia (ALL). The authors have noted a high percentage of mosaic karyotypes (75.0%) with a predominance of abnormal clones combined with normal karyotypes (33.3%). Trisomies of chromosomes led to the formation of hyperdiploid clones, among which trisomies of chromosomes 6, 21, 15, and 5 were the most frequent events. Additional marker chromosomes were recorded in 22.2%. To characterize the mechanisms underlying the abnormal clone formation in relapse of ALL, structural chromosomal anomalies were recorded and divided into balanced (translocations, inversions) and imbalanced (deletions, isochromosomes, additional material of unknown origin, duplications, and imbalanced translocations) abnormalities. Losses of genetic material (deletions) (24.1%) and translocations (33.3%) were most frequently detected. The total number of events with translocation t(9;22)(q34;q11.2) reached 20.4%. The evolution of clonal chromosomal abnormalities occurred due to the emergence of additional numerical and imbalanced structural abnormalities. The comparison between chromosome abnormalities at diagnosis and in relapse of B-cell ALL has not led to any general mechanisms for the formation of chemotherapy-resistant clones. Trisomy of chromosome 5, deletion del(6)(q23), and translocation t(9;22) (q34;q11.2) were involved in the formation of chemotherapy-insensitive clones. The group of unfavorable prognosis included 95.8% of karyotypes.

摘要 对 24 名急性淋巴细胞白血病(ALL)复发患者的骨髓细胞进行了细胞遗传学重排研究。作者注意到马赛克核型的比例很高(75.0%),其中以异常克隆合并正常核型为主(33.3%)。染色体三体导致超二倍体克隆的形成,其中以 6、21、15 和 5 号染色体三体最为常见。22.2%的患者出现了额外的标记染色体。为了确定 ALL 复发时异常克隆形成的机制,我们记录了染色体结构异常,并将其分为平衡异常(易位、倒位)和不平衡异常(缺失、同源染色体、来源不明的附加物质、重复和不平衡易位)。最常发现的是遗传物质缺失(缺失)(24.1%)和易位(33.3%)。发生t(9;22)(q34;q11.2)易位的病例总数占20.4%。克隆染色体异常的演变是由于出现了额外的数量和结构不平衡异常。对 B 细胞 ALL 诊断时和复发时的染色体异常进行比较,尚未发现化疗耐药克隆形成的一般机制。5号染色体三体、del(6)(q23)缺失和t(9;22)(q34;q11.2)易位参与了化疗不敏感克隆的形成。预后不良组包括95.8%的核型。
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引用次数: 0
Impact of Different DNA Ploidy Patterns on Endometrial Carcinomas Based on Image Cytometry 基于图像细胞测量的不同 DNA 倍性模式对子宫内膜癌的影响
IF 0.5 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2024-02-01 DOI: 10.3103/s0095452724010092

Abstract

Worldwide, endometrial cancer is one of the most frequently diagnosed malignancies in women and a notable cause of death. The aim of this study was to perform image cytometric DNA ploidy analysis on a prospective material of endometrial adenocarcinomas in order to determine potential correlation between ploidy status and their histological features. The analysis was carried out in fresh tissue samples resected by implementing complete hysterectomy in a series of patients (n = 126). We found that ploidy status using image cytometry correlate with histologic type, grade and stage in endometrial cancer and aneuploid tumor samples are associated with aggressive phenotype statistics. Furthermore, DNA ploidy should be used as a reliable and applicable prognostic marker in the routine clinical practice.

摘要 在世界范围内,子宫内膜癌是妇女最常诊断出的恶性肿瘤之一,也是导致妇女死亡的一个重要原因。本研究旨在对子宫内膜腺癌的前瞻性材料进行图像细胞学 DNA 倍性分析,以确定倍性状态与其组织学特征之间的潜在相关性。分析是在一系列患者(n = 126)实施全子宫切除术后切除的新鲜组织样本中进行的。我们发现,使用图像细胞仪检测的倍性状态与子宫内膜癌的组织学类型、分级和分期相关,非整倍体肿瘤样本与侵袭性表型统计相关。此外,在常规临床实践中,DNA 倍性应作为一种可靠、适用的预后标志物。
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引用次数: 0
Consequence of Gamma Radiation Induced Cytomixis during Microsporogenesis in Fennel Plant (Foeniculum vulgare Mill.) 伽马辐射诱导茴香(Foeniculum vulgare Mill.)小孢子发生过程中细胞混合的后果
IF 0.5 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2024-02-01 DOI: 10.3103/s0095452724010109

Abstract

Fennel is considered as a very important spice crop with powerful therapeutic potential. An improvement in this valuable crop, selected physical mutagen (Gamma irradiation) on the seeds with five selective doses viz., 50, 100, 150, 200 and 250 Gy for break genetic consistency in narrow genetic base in Fennel crop, remunerative phenomenon of syncytes was seen in some cases, where complete chromatin was transmitted to the recipient PMC, that generates dimorphic pollen grain. Such pollen grain with varying genetic content plays a significant role in the emergence of intraspecific polyploidization of species. A curious biological process which is often observed in microsporogenesis of higher plants like, development of syncytes, cytomixis between plant cells and due to this the creation of big pollen has evolutionary relevance. The cytomictic behaviour of Foeniculum vulgare Mill. has been reported in this experiment.

摘要 茴香被认为是一种非常重要的香料作物,具有强大的治疗潜力。为了改良这种珍贵的作物,研究人员选择了物理诱变剂(伽马射线辐照),对种子进行了 50、100、150、200 和 250 Gy 五种选择性剂量的辐照,以打破茴香作物遗传基础狭窄的遗传一致性,在某些情况下出现了合子现象,完整的染色质被传递到受体 PMC,从而产生二态花粉粒。这种具有不同遗传内容的花粉粒在物种的种内多倍体化过程中起着重要作用。在高等植物的小孢子发生过程中,经常会观察到一个奇特的生物过程,如合子的发育、植物细胞间的细胞混合,因此大花粉的产生与进化有关。本实验报告了茴香(Foeniculum vulgare Mill.)的细胞混合行为。
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引用次数: 0
Activity of Nonnucleoside Inhibitors of O6-methylguanine-DNA Methyltransferase Repair Enzyme in Human Cells In Vitro 体外研究o6 -甲基鸟嘌呤- dna甲基转移酶修复酶非核苷类抑制剂的活性
IF 0.5 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2023-12-04 DOI: 10.3103/s0095452723060105
K. S. Zhuvaka, G. P. Volynets, T. P. Ruban, Z. M. Nidoeva, A. P. Iatsyshyna, L. L. Macewizc, V. G. Bdzhola, S. M. Yarmoluk, L. L. Lukash

Abstract

The repair enzyme O6-methylguanine-DNA methyltransferase (MGMT) eliminates alkyl lesions that play the main anticancer role in alkylating chemotherapy. The inhibition of MGMT leads to increasing effectiveness of alkylating chemotherapy. In this study, new potential MGMT inhibitors were tested. It was found that some compounds demonstrate low cytotoxicity and high effectiveness in human cells in vitro.

摘要修复酶o6 -甲基鸟嘌呤- dna甲基转移酶(MGMT)可清除烷基化化疗中起主要抗癌作用的烷基病变。MGMT的抑制导致烷基化化疗的有效性增加。在这项研究中,新的潜在的MGMT抑制剂进行了测试。研究发现,一些化合物在体外对人体细胞具有低细胞毒性和高活性。
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引用次数: 0
Transition Bias and Its Compensation in the Evolutionary Lineage of the Subfamily Murinae (Rodentia): Analysis of Nuclear and Mitochondrial DNA Markers 鼠亚科进化谱系中的过渡偏差及其补偿:核和线粒体DNA标记分析
IF 0.5 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2023-12-04 DOI: 10.3103/s0095452723060051
S. V. Mezhzherin, S. Yu. Morozov-Leonov, V. O. Tereshchenko

A comparative analysis of the rates of molecular evolution, transition bias, and its evolutionary compensation was carried out on mitochondrial (D-loop, Cytb, COI, 12S RNA) and nuclear (IRBP, Fv) DNA markers in the Murinae subfamily. According to the levels of variability, the markers can be divided into three classes: (1) hypervariable (D-loop), (2) rapidly evolving (Cytb, COI), and (3) conservative (12S RNA, IRBP, Fv). The nature of nucleotide substitutions appears by the levels of variability. With the D-loop, there is a maximum initial bias, which is already partially compensated for during the early stages of speciation, and completely compensated at the stages of species divergence. The pronounced bias within the Cytb and COI genes is only partially compensated, moreover at the genus levels. The 12S RNA, IRBP, and Fv genes with a low level of transition bias do not show evolutionary compensation as such, and the decrease of the ts/tv index in the evolutionary lineage has a technical character and is a consequence of a relative decrease of the difference in the frequencies of transitions and transversions against the background of an absolute increase in the frequencies of substitutions. The positive relationship between the intensity of nucleotide substitutions, the level of transition bias, and the rates of its evolutionary compensation proves that these phenomena have the same primary basis.

对Murinae亚科的线粒体(D-loop、Cytb、COI、12S RNA)和核(IRBP、Fv) DNA标记进行了分子进化速率、过渡偏差及其进化补偿的比较分析。根据可变性水平,标记可分为三类:(1)高变(D-loop),(2)快速进化(Cytb, COI),(3)保守(12S RNA, IRBP, Fv)。核苷酸取代的本质表现为可变性的程度。对于d环,存在最大的初始偏差,在物种形成的早期阶段已经部分补偿,并在物种分化阶段完全补偿。Cytb和COI基因中明显的偏倚仅在属水平上得到部分补偿。具有低水平过渡偏差的12S RNA、IRBP和Fv基因没有表现出这样的进化补偿,进化谱系中ts/tv指数的下降具有技术特征,是在取代频率绝对增加的背景下过渡和翻转频率差异相对减少的结果。核苷酸取代强度、过渡偏倚水平及其进化补偿率之间的正相关关系证明了这些现象具有相同的初级基础。
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引用次数: 0
Development of Winter Common Wheat Lines with the Stem Rust Resistance Gene Sr33 小麦茎秆抗锈病基因Sr33的选育
IF 0.5 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2023-12-04 DOI: 10.3103/s009545272306004x
N. O. Kozub, Ya. V. Pirko, I. O. Sozinov, A. V. Karelov, O. I Sozinova, B. V. Ivashchuk, G. Fedak, A. I. Yemets, Ya. B. Blume

Stem rust caused by the fungus Puccinia graminis Pers. is a dangerous disease of wheat that occurs in all regions of its cultivation. New highly virulent races causing severe yield losses have appeared in recent decades. Sr33 introgressed from Aegilops tauschii is one of the genes conferring resistance against most races of stem rust, including Ug99. To develop winter common wheat lines with the gene Sr33 and evaluate a possible effect of the gene on yield traits, the authors made a cross between the spring line DH31 carrying the Sr33 gene and the winter cultivar Myrkhad followed by marker-assisted selection of winter genotypes with Sr33 starting from F3. To identify the Sr33 gene, PCR with the gene-specific marker Sr33A was used. Alleles at the storage protein loci of the parental forms were identified using acid polyacrylamide gel electrophoresis and SDS-electrophoresis as well as the molecular marker MAR for Glu-Blal. As a result of marker-assisted selection, winter F5 lines with the Sr33 gene were developed from the cross DH31 × Myrkhad. The yield traits of F5 spikes of families derived from single F3 spikes with and without Sr33 were analyzed considering that the line DH31 has a specific allele at Gli-D1 from Ae. tauschii, dark glumes, and high molecular weight glutenin subunit alleles associated with high dough strength, in particular, Glu-Blal. Comparison of means of yield traits of spikes from families with Sr33 and without it did not reveal significant differences between these two groups. Thus, winter F5 lines with the Sr33 gene from the cross DH31 × Myrkhad may be used in the breeding practice to develop cultivars with high bread-making qualities of flour and stem rust resistance.

由小麦锈菌引起的茎锈病。是小麦的一种危险病害,发生在其所有种植区域。最近几十年出现了造成严重产量损失的新的高毒力品种。Sr33基因是黄斑鱼(Aegilops tauschii)对大多数茎锈病(包括Ug99)具有抗性的基因之一。为了选育具有Sr33基因的冬季普通小麦品系,并评价该基因对产量性状的影响,作者将携带Sr33基因的春季品系DH31与冬季品种Myrkhad进行杂交,然后从F3开始用Sr33进行冬季基因型的标记辅助选择。采用Sr33A基因特异性标记PCR鉴定Sr33基因。利用酸性聚丙烯酰胺凝胶电泳和sds -电泳以及Glu-Blal分子标记MAR对亲本储存蛋白位点的等位基因进行了鉴定。通过标记辅助选择,从DH31 × Myrkhad杂交组合中获得了Sr33基因的冬季F5系。考虑到DH31系具有来自伊蚊的Gli-D1特异等位基因,对含Sr33和不含Sr33的F3单穗衍生的家族F5穗的产量性状进行了分析。与高面团强度相关的高分子量谷蛋白亚基等位基因,特别是Glu-Blal。对含Sr33和不含Sr33家系的穗产量性状均值进行比较,两组间差异不显著。因此,从DH31 ×麦哈德杂交中获得Sr33基因的冬季F5系可用于育种实践,开发具有高面粉品质和茎锈病抗性的品种。
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引用次数: 0
Erratum to: Remodeling the Architecture of Collagen-Containing Connective Tissue Fibers of Metastatic Prostate Cancer 对转移性前列腺癌含胶原结缔组织纤维结构的重塑的勘误
IF 0.5 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2023-12-04 DOI: 10.3103/s0095452723060129
L. A. Naleskina, N. Yu. Lukianova, T. V. Zadvornyi, L. M. Kunska, O. M. Mushii, V. F. Chekhun

An Erratum to this paper has been published: https://doi.org/10.3103/S0095452723060129

本文的勘误表已发表:https://doi.org/10.3103/S0095452723060129
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引用次数: 0
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