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双语推荐:Sox9b

利用简并引物SoxN和Sox9在鳙基因组DNA中进行PCR扩增和产物克隆测序,并对序列进行同源性比较和系统进化分析。结果表明本文鉴定出鳙15个Sox基因HMG盒序列,分别属于SoxB、SoxC和SoxE组,依据斑马鱼同源基因将其分别命名为Sox1a、Sox1b、Sox2、Sox3、Sox4a、Sox4b、Sox9a、Sox9b、Sox10、Sox11b、Sox12、Sox14a、Sox14b、Sox19和Sox21a。基于鳙和斑马鱼Sox1、Sox4和Sox9基因核苷酸序列构建的系统进化树显示这3个Sox基因的复制时间发生在鳙和斑马鱼的分化之前,结果支持了鱼类特异的基因组复制假说。以Sox1a、Sox1b和Sox4基因为分子钟标记构建系统进化树探讨鳙和斑马鱼的分化时间,结果显示,同属于鲤科鱼类的鳙(鲤亚科)和斑马鱼(鱼丹亚科)在原始的鱼丹亚科鱼类中存在一个共同祖先,大约出现在63.7百万年前。研究结果为进一步研究鱼类Sox基因复制和基因组进化等问题提供了重要参考资料。
To amplify Sox genes from bighead carp genome, two pairs of degenerate primers (SoxN and Sox9) were de-signed for PCR amplification that were utilized for sequencing and analysis of sequence homology and phylogenetic relationships. The results showed that 15 distinct Sox genes encoding the HMG domains were identified in bighead carp, which were assigned to group B, C and E. According to their homology to orthologs of zebrafish, 15 Sox genes were designated as Sox1a, Sox1b, Sox2, Sox3, Sox4a, Sox4b, Sox9a, Sox9b, Sox10, Sox11b, Sox12, Sox14a, Sox14b, Sox19 and Sox21a, respectively. Phylogenetic tree of Sox1, Sox4 and Sox9 nucleotide sequences indicated that the duplication of these three Sox genes occurred before the divergence of bighead carp and zebrafish, and this observation supported the“fish-specific whole-genome duplication” theory. Using Sox1a, Sox1b and Sox4 as molecular clock markers in phy-logenetic analysis, the estimation of the divergence time between bighead c

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通过整体原位杂交和切片原位杂交技术系统全面地比较分析了斑马鱼胚胎四个发育时期(12、24、48 hpf和4 dpf)和成熟性腺中Sox9a和Sox9b基因的表达模式。结果显示,两个Sox9基因在脑和眼中持续表达,但在耳囊、头部软骨、胸鳍芽和体节中差异性表达。 Sox9a特异性地在侧线、尾部神经嵴、原肾管和精巢支持细胞中表达,而Sox9b在卵巢的卵黄颗粒中大量表达。与已发表的研究结果相比,本研究更广泛地揭示了Sox9a和Sox9b的动态差异表达模式,且更清楚地显示了其在性腺中的表达特征。
Using whole mount and tissue section in situ hybridization techniques , the expression patterns of two Sox9 homologues genes ,Sox9a and Sox9b,were comprehensively compared and analyzed in four stages of developing embryo (12, 24, 48 hpf and 4 dpf) and mature gonads of zebrafish (Danio rerio).The two genes were persistently expressed in brain and eyes ,but differentially expressed in otic vesicle , head cartilage , pectoral fin buds and somites .Distinct from high expression of Sox9b in the yolk granules of oocytes, Sox9a was specifically expressed in lateral line , tail neural crest , primary renal tubular and Sertoli cells in testis . Compared with other published results , the present data revealed a more extensive differential expression pro-file of two Sox9 genes in the developing embryo and gonads of zebrafish .

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探讨SOX11在各型B细胞非霍奇金淋巴瘤中表达的差异。方法:对B细胞非霍奇金淋巴瘤103例应用免疫组化方法检测SOX11的表达。结果:12例反应性增生中不表达SOX11,套细胞淋巴瘤21例中19例(90.5%)细胞核表达SOX11,弥漫大B细胞淋巴瘤45例中细胞核表达15例(33.3%),滤泡性淋巴瘤11例中细胞核表达4例(36.4%),伯基特淋巴瘤9例中细胞核表达2例(22.2%),小淋巴细胞淋巴瘤13例中细胞核散在弱阳性1例(7.7%),淋巴结边缘区淋巴瘤4例中细胞核中度表达1例(25.0%),SOX11在套细胞淋巴瘤的表达率和其他类型淋巴瘤比较差异有统计学意义(P0.05)。结论:SOX11蛋白可在多种不同类型的B细胞性淋巴瘤中表达,在MCL中的表达率明显高于其它类型淋巴瘤。
Objective: To evaluate the expression of transcription factor SOX11 in B-cell non-Hodgkin lymphoma. Methods: Immunostaining of two-step EnVision method was used to detect SOX11 expression in paraffin sections of 103 patients with B-cell non-Hodgkin lymphoma. Results: In RH of lymph nodes, all cases did not express SOX11. 19 of the 21 MCL expressed strong staining of SOX11 on nuclei. 15 of the 45 (33.3%)cases of DLBCL, 4 of the 11 (36.4%) FL, 2 of the 9 (22.2%)BL, and 1 of the 4 (25.0%) N-MZL also showed weak or medium staining of SOX11 on nuclei. In 1 case of the 13 SLL, SOX11 were sparsely expressed on the nuclei of medium size cells. SOX11 nucleus expression rates were different of statistical significance among MCL and other types(P<0.001). Conclusions: (1) SOX11 could express multiple different types of lymphomas, but did not express on the reactive lymphocytes in lymphomas, which might suggest that SOX11 was related to the genesis of some types of lymphomas. (2) SOX11 expressive r
研究细胞自噬水平改变后,对小鼠骨髓间充质干细胞(bone marrow mesenchymal stem cells,BMMSCs)干性标记基因Nanog、Oct-4、Sox-Ⅱ表达的影响。方法:分离培养小鼠BMMSCs,经表型鉴定后,分别利用自噬激活剂雷帕霉素(rapamycin)和靶向作用于beclin 1的si-RNA(small interfernce RNA target beclin 1,si-beclin 1)激活或抑制小鼠BMMSCs的自噬活性;利用实时定量PCR仪(Real-time PCR,RT-PCR)检测各组BMMSCs的各自噬相关基因以及干性标记基因的表达水平。结果:流式细胞仪检测结果显示,小鼠BMMCs中CD90.2、CD29、SCA-1的阳性率分别为97.4%、97.6%、83.5%,CD31、CD146、CD11b的阳性率分别为2.9%、2.4%、5.6%;雷帕霉素激活BMMSCs自噬后,其干性标记基因Nanog、Oct-4、Sox-Ⅱ的表达均较对照组明显升高(P0.05),而用si-beclin 1抑制BMMSCs的自噬活性后,Nanog、Oct-4、Sox-Ⅱ的表达均较对照组明显下降(P0.05)。结论:提高BMMSCs的自噬水平有助于保持干细胞的特异性基因表达。
AIM:To study the effect of autophagy on the expression of stemness marker gene Nanog,Oct-4 and Sox-Ⅱ in mouse bone marrow mesenchymal stem cells(BMSCs).METHODS:Mouse BMMSCs were isolated, cultured and identified by flow cytometry analysis.Autophagy of BMSCs was induced by rapamycin or inhibited by siR-NA targeting beclin-1 (si-beclin 1 ),the level of autophagy of BMMSCs and the expression of Nanog,Oct-4 and Sox-Ⅱ were examined by Real Time PCR (RT-PCR).RESULTS:The cultured BMMSCs expressed CD90.2 (97.4%),CD29 (97.6%),SCA-1 (83.5%),CD31(2.9%),CD146 (2.4%)and CD11b (5.6%).Treatment with rapamycin increased Nanog,Oct-4 and Sox-Ⅱexpression (P<0.05),whereas,si-beclin 1 decreased the auto-phagy acticity and down-regulated Nanog,Oct-4 and Sox-Ⅱ expression (P<0.05)of BMMSCs.CONCLUSION:Increasing autophagy activity of BMMSCs may be favourable for the cells to maintain the stemness.

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上、下颌骨的发育差异可能是由于两者差异性地表达某些基因而造成的。本文拟对E9.5(胚胎第9.5天)小鼠上、下颌弓差异性表达的基因进行系统的生物信息学分析。方法:从GEO数据库获取E9.5小鼠上、下颌弓差异性表达的基因,应用DAVID和Gene MANIA数据库分析这些基因之间的相互关系。结果:经过DAVID数据分析,这些在E9.5小鼠上、下颌弓差异性表达的基因被富集到不同的生物学过程或分子功能的子集中,如"转录因子活性"、"系统发育"和"骨骼系统发育"等。其中BTB7B、SOX10、TSHZ2、GSC、GLIS2、MEIS1、CITED2、IRF9、BARX1、MSX1、DLX6、CSRNP1、HEYL、MKX、PITX1和NFIB,这16个基因被富集到"转录因子活性"这一分子功能子集。通过Gene MANIA数据库分析,建立了这16个基因及一些预测基因的分子网络图,显示这些基因存在直接或间接的相互作用。结论:上、下颌骨在发育过程中存在许多差异表达的基因,其中对上、下颌骨特异性发育具有重要调控作用的16个转录因子包括BTB7B、SOX10、TSHZ2、GSC、GLIS2、MEIS1、CITED2、IRF9、BARX1、MSX1、DLX6、CSRNP1、HEYL、MKX、PITX1和NFIB,它们彼此密切相关且相互作用形成调控网络。在研究上、下颌骨差异性发育的分子调控机制时,需要关注由这些
Objective: The aim of this study was to perform a systematic bioinformatic analysis in differentially expressed genes between the E9.5 mouse maxillary and mandibular arch. Methods: The differentially expressed genes between the E9.5 mouse maxillary and mandibular arch were obtained from the gene expression omnibus database (GEO Datasets). Then the DAVID and GeneMANIA database were used to analyse the relationships during these genes. Results: These differentially expressed genes between the E9.5 mouse maxillary and mandibular arch could be enriched into different "biological process" and "molecular function" subgroups, based on the analysis of DAVID database, including "transcription factor activity", "system development", "skeleton system development", etc. Sixteen genes, including BTB7B, SOX10, TSHZ2, GSC, GLIS2, MEIS1, CITED2, IRF9, BARX1, MSX1, DLX6, CSRNP1, HEYL, MKX, PITX1 and NFIB, were enriched into the "transcription factor activity" subgroup, and these genes were cl

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常的性腺分化可分为3个过程:原始性腺形成、性别决定和卵巢/睾丸发育。在任一环节中,基因表达或调控发生异常均有可能导致性发育异常疾病的发生。性发育异常是指染色体、性腺和解剖性别不典型。随着分子生物学技术的发展,不断地发现新的基因或信号通路参与性腺分化和发育,如SRY、SF1、W T1、Sox9等基因与睾丸发育密切相关,Wnt/Rspo1/B连环蛋白通路、Dax1、Foxl2等基因在卵巢分化中发挥着重要作用,一些非编码RNA和转化生长因子也有重要的调节功能,且睾丸和卵巢发育均为主动过程,即使在出生后因某些基因的改变两者间也可出现横向分化。这些为揭示性分化异常的发病机制提供了可能。
Normal sex differentiation includes the formation of primordial gonads, sex determination and ovarian or testis development. The misregulation of gene expression in each process may lead to the disorders of sex development (DSD). DSD is defined by congenital conditions of the atypical chromosome,gonadal or anatomical sex. With the development of molecular biotechnology,more and more genes and signaling pathways are discovered to be involved in sex differentiation and development. For example,some genes such as SRY、SF1、W T1 and Sox9 are closely related to testicular development, while others such as Wnt/Rspo1/B-catenin pathway and genes like Dax1、Foxl2 play an important role in ovarian differentiation. Some none-coding RNA and transforming growth factor also regulate the sexual differentiation. The developments of both testis and ovary are active, and transverse differentiation can appear according to some abnormal genes even after birth.

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目的检测IL-1β对ATDC5成软骨分化细胞miR-455-3p表达的影响,探索miR-455-3p在骨关节炎中的作用。方法诱导ATDC5细胞成软骨分化后,予10 ng/ml的IL-1β刺激,在刺激4、12、24、48 h时应用实时荧光定量PCR检测miR-455-3p、C/EBPβ和软骨特征性标记物的表达情况;并利用抑制剂IKK-NBD阻断NF-κB通路后,应用实时荧光定量PCR检测IL-1β作用下miR-455-3p的表达水平。结果在IL-1β作用下的ATDC5成软骨分化细胞中miR-455-3p、C/EBPβ和软骨退变标记物(MMP13、ADAMTS5)均上调,而软骨基质合成标记物(ACAN、COL2A1、SOX9)则下调,且后期更为明显;而IKK-NBD可抑制IL-1β诱导的miR-455-3p表达。结论 IL-1β可上调ATDC5成软骨分化细胞miR-455-3p的表达水平,且受NF-κB通路的调节。
Objective To investigate the effects of IL-1 beta ( IL-1β) on the expression of miR-455-3p in the differentiated ATDC5 cells.Methods After chondrogenic differentiation , ATDC5 cells were treated with 10ng/ml recombinant murine IL-1βfor different time length.Additionally, a NF-kappaB inhibitor IKK-NBD was added to the cell culture before the IL-1βtreatment.The expression of miR-455-3p, C/EBP βand the genes related to cartilage were detected by quantitative real-time PCR.ResultsThe IL-1β-treat differentiated ATDC5 cells increased the expression of miR-455-3p, C/EBP β, MMP13 and ADAMTS5, while decreased the expression of ACAN , COL2A1 and SOX9 especially in the late stage. IL-1β-induced up-regulation of miR-455-3p was inhibited by IKK-NBD.Conclusion The expression of miR-455-3p in the differentiated ATDC5 cells can be induced by IL-1βand NF-kappa B is involved in the up-regulation.

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目的 本研究旨在探讨初诊急性B淋巴细胞白血病(B-ALL)患儿骨髓中干性基因的表达及其与临床预后指标的关系.方法 应用Real-time PCR检测32例初诊B-ALL患儿(B-ALL组)和5例骨髓象正常儿童(对照组)的骨髓单个核细胞上干性基因(Oct4、JAG1、Nanog、Sox2、Fgf4等)的表达,比较B-ALL组和对照组的差异,在此基础上结合临床资料(如性别、年龄、外周血白细胞、危险度分层等)进行相关性分析.结果 B-ALL组儿童的相关于性基因Nanog、JAG1、CD133-2、CD44和Runx1的表达水平较对照组明显增高,分别为对照组的2.74±1.00、4.31 ±2.41、10.23±3.21、4.66±1.73和7.44±3.01倍(P<0.01),Oct4、Sox2、D LL1、Fgf4和COX-2表达水平较对照组明显降低,分别为对照组的15.00%±0.06、13.00%±0.08、18.12%±0.11、4.73%±0.03和9.59%±0.00(P <0.01);初诊B-ALL组干性基因表达与其性别、年龄、外周血白细胞计数、骨髓幼稚细胞比例、FAB分型、细胞遗传学异常、融合基因表达等均无相关性,其中JAG1基因表达与B-ALL危险度分层有明显相关性(r=0.755,P<0.01),其余基因表达与危险度分层无明显相关.结论 与正常儿童的骨髓相比较,初诊B-ALL患儿骨髓中干性基因存在异常表达(上调或下调),其中JAG1基因
Objective This study investigated the expression of stem genes in bone marrow cells and its relationship with clinical prognostic factors in childhood with B linage acute lymphoblastic leukemia (BALL) at initial diagnosis.Methods Real-time PCR was applied to detect the expression of stem genes(Oct4,JAG1,Nanog,Sox2,Fgf4.etc) in bone marrow of 32 childhood B-ALL patients (B-ALL group) and 5 normal children (control group).The gene expression differences in 2 groups were compared.Their relationship with clinical prognostic factors (e.g.gender,age,white blood cell count,risk stratification,etc.) were assayed.Results:In B-ALL group,the expression of Nanog,JAG1,CD133-2,CD44 and Runx1 was significantly higher than those of control group (P < 0.01).They were 2.74 ± 1.04,4.31 ± 2.41,10.23 ± 3.21,4.66 ± 1.73 and 7.44 ± 3.01 times that of their control groups respectively.While the expression of Oct4,Sox2,DLL1,Fgf4 and COX-2 was statistically lower than those of control group (P

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目的 探讨通过悬浮培养法富集乙醛脱氢酶1(ALDH-1)高表达的头颈部鳞癌肿瘤细胞的可行性,鉴定富集的细胞是否具有肿瘤干细胞特性.方法 将头颈肿瘤细胞株接种于低黏附平板,在10 ng/ml重组表皮生长因子和10 ng/ml碱性成纤维细胞生长因子的无血清培养基中形成细胞微球,通过ALDEFLUOR方法对ALDH-1的表达水平进行半定量分析,采用流式细胞术分选出ALDH-1高表达细胞,分析其生物学特性.结果 UD-SCC1、UT-SCC22、UM-SCC11B、UT-SCC9和UT-SCC24A细胞在无血清培养液中悬浮培养5~1Od后均能形成细胞微球.在UD-SCC1、UT-SCC22、UM-SCC11B、UT-SCC9和UT-SCC24A细胞株细胞微球来源的细胞(SDC)中,ALDH-1的表达水平均高于其贴壁生长细胞(均P<0.05).ALDH-1高表达和低表达细胞形成的克隆细胞数分别为(197±47)个和(33±16)个(P<0.01).单个ALDH-1高表达和低表达UT-SCC9细胞的克隆形成率分别为17.1%和0.7%,差异有统计学意义(P<0.05);单个ALDH-1高表达和低表达UD-SCC1细胞的克隆形成率分别为19.3%和0,差异有统计学意义(P<0.01).UD-SCC1、UT-SCC22、UM-SCC11B、UT-SCC9和UT-SCC24A细胞的SDC侵袭力均高于其贴壁细胞(均P<0.05).在UD-SCC1、UT-SCC22、UM-SCC11B、UT-SCC9和UT-SCC24A细胞的SDC中,Nanog、Sox2和Oct-4 mRNA的表达水平均高于其贴壁细胞(均P<0.05).UD-SCC1和UT-SCC24A细胞的SDC中,低活性氧簇(ROS)水平细胞比例分别为(26.3±4.9)%和(72.1±6.1)%,均高于UD-SCC1和UT-SCC24A细胞的贴壁细胞中低ROS水平细胞比例[分别为(8.6±1.7)%和(23.7±7.5)%,均P<0.05].结论 悬浮培养法可有效富集头颈部鳞癌细胞系内的ALDH-1高表达细胞,富集后的细胞具有肿瘤干细胞特性.
Objective Initiation,growth,recurrence,and metastasis of head and neck squamous cell carcinoma (HNSCC) have been related to the cancer stem cells (CSC) that can be identified by their aldehyde-dehydrogenase-isoform-1 (ALDH-1) activity.In this study,we try to prove that suspension culture can enrich ALDH-1 high expression cells within HNSCC cell lines and the enriched cells possess cancer stem cell properties.Methods Cells from five HNSCC cell lines were cultured in ultra-low attachment plates in serum-free Quantum 263 medium supplemented with 10 ng/ml EGF and 10 ng/ml bFGF,and ALDH-1 expression level was evaluated by ALDEFLUOR assay.ALDH-1 high expression cells were separated by FACS sorting,and their phenotypical and functional properties were characterized.Results Spheroids can be formed from all five HNSCC cell lines (UD-SCC1,UT-SCC22,UM-SCC11B,UT-SCC9 and UTSCC24A) under anchorage independent culture condition.The proportion of ALDH1 high expression cells were highly increased in s

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