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Yong Wang Keping Chen Qin Yao Xiaodong Zheng Zhe Yang 《Journal of molecular evolution》2009,68(6):629-640
The basic helix-loop-helix (bHLH) proteins play important regulatory roles in eukaryotic developmental processes including
neurogenesis, myogenesis, hematopoiesis, sex determination, and gut development. Zebrafish is a good model organism for developmental
biology. In this study, we identified 139 bHLH genes encoded in the zebrafish genome. Phylogenetic analyses revealed that zebrafish has 58, 29, 21, 5, 19, and 5 bHLH members
in groups A, B, C, D, E, and F, respectively, while 2 members were classified as “orphan.” A comparison between zebrafish
and human bHLH repertoires suggested that both organisms have a certain number of specific bHLH members. Eight zebrafish bHLH genes were found to have multiple coding regions in the genome. Two of these, Bmal1 and MITF, are good anchor genes for identification of fish-specific whole-genome duplication events in comparison with mouse and chicken
genomes. The present study provides useful information for future studies on gene family evolution and vertebrate development.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
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Michael K. Skinner Alan Rawls Jeanne Wilson-Rawls Eric H. Roalson 《Differentiation; research in biological diversity》2010
A phylogenetic analysis of the basic helix-loop-helix (bHLH) gene superfamily was performed using seven different species (human, mouse, rat, worm, fly, yeast, and plant Arabidopsis) and involving over 600 bHLH genes ( Stevens et al., 2008). All bHLH genes were identified in the genomes of the various species, including expressed sequence tags, and the entire coding sequence was used in the analysis. Nearly 15% of the gene family has been updated or added since the original publication. A super-tree involving six clades and all structural relationships was established and is now presented for four of the species. The wealth of functional data available for members of the bHLH gene superfamily provides us with the opportunity to use this exhaustive phylogenetic tree to predict potential functions of uncharacterized members of the family. This phylogenetic and genomic analysis of the bHLH gene family has revealed unique elements of the evolution and functional relationships of the different genes in the bHLH gene family. 相似文献
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The giant panda (Ailuropoda melanoleuca) is a critically endangered mammalian species. Studies on functions of regulatory proteins involved in developmental processes would facilitate understanding of specific behavior in giant panda. The basic helix-loop-helix (bHLH) proteins play essential roles in a wide range of developmental processes in higher organisms. bHLH family members have been identified in over 20 organisms, including fruit fly, zebrafish, mouse and human. Our present study identified 107 bHLH family members being encoded in giant panda genome. Phylogenetic analyses revealed that they belong to 44 bHLH families with 46, 25, 15, 4, 11 and 3 members in group A, B, C, D, E and F, respectively, while the remaining 3 members were assigned into "orphan". Compared to mouse, the giant panda does not encode seven bHLH proteins namely Beta3a, Mesp2, Sclerax, S-Myc, Hes5 (or Hes6), EBF4 and Orphan 1. These results provide useful background information for future studies on structure and function of bHLH proteins in the regulation of giant panda development. 相似文献
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The DYT1‐interacting proteins bHLH010, bHLH089 and bHLH091 are redundantly required for Arabidopsis anther development and transcriptome
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Engao Zhu Chenjiang You Shuangshuang Wang Jie Cui Baixiao Niu Yingxiang Wang Ji Qi Hong Ma Fang Chang 《The Plant journal : for cell and molecular biology》2015,83(6):976-990
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Stevens JD Roalson EH Skinner MK 《Differentiation; research in biological diversity》2008,76(9):1006-1022
A phylogenetic analysis of seven different species (human, mouse, rat, worm, fly, yeast, and plant) utilizing all (541) basic helix-loop-helix (bHLH) genes identified, including expressed sequence tags (EST), was performed. A super-tree involving six clades and a structural categorization involving the entire coding sequence was established. A nomenclature was developed based on clade distribution to discuss the functional and ancestral relationships of all the genes. The position/location of specific genes on the phylogenetic tree in relation to known bHLH factors allows for predictions of the potential functions of uncharacterized bHLH factors, including EST's. A genomic analysis using microarrays for four different mouse cell types (i.e. Sertoli, Schwann, thymic, and muscle) was performed and considered all known bHLH family members on the microarray for comparison. Cell-specific groups of bHLH genes helped clarify those bHLH genes potentially involved in cell specific differentiation. This phylogenetic and genomic analysis of the bHLH gene family has revealed unique aspects of the evolution and functional relationships of the different genes in the bHLH gene family. 相似文献
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Megan E. Andriankaja Selahattin Danisman Lorin F. Mignolet-Spruyt Hannes Claeys Irina Kochanke Mattias Vermeersch Liesbeth De Milde Stefanie De Bodt Veronique Storme Aleksandra Skirycz Felix Maurer Petra Bauer Per Mühlenbock Frank Van Breusegem Gerco C. Angenent Richard G. H. Immink Dirk Inzé 《Plant molecular biology》2014,85(3):233-245
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bHLH转录因子在植物的生长发育、胁迫应答和次生代谢中具有重要的调控作用。该研究通过PCR技术从银杏(Ginkgo biloba)叶中分离得到了一个bHLH基因的cDNA序列,并将其命名为GbbHLH91。序列分析结果显示扩增的GbbHLH91基因cDNA序列长度为1 425 bp,开放阅读框是1 065 bp,编码354个氨基酸,分子量为40.1 kDa,等电点为8.20。系统进化分析结果显示,从用于进化树构建的bHLH蛋白质聚类情况来看,银杏GbbHLH91蛋白与裸子植物油松(Pinus tabuliformis)bHLH蛋白亲缘关系最近,且与被子植物无油樟(Amborella trichopoda)bHLH蛋白相似性达到60%,表明该基因在进化过程中相对比较保守。实时荧光定量PCR分析发现银杏bHLH91基因在银杏的各个组织中均有表达,其中在银杏叶中表达量最高,在根和茎中基因的表达量次之,在银杏雌花和果中表达量较少,在雄花中的表达水平最低;GbbHLH91基因在不同发育时期的银杏叶片中,表达量也存在一定的差异,其中在4月中旬该基因的表达水平达到最高,而后随着叶片的生长发育,该基因的表达水平呈现下降趋势。该研究结果为进一步验证GbbHLH91基因的功能奠定了前期基础。 相似文献
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Jacobus Hendricks Peter Terpstra Peter M. Dammers Rajesh Somasundaram Annie Visser Maaike Stoel Nicolaas A. Bos Frans G. M. Kroese 《Immunogenetics》2010,62(7):479-486
We have mapped and annotated the variable region of the immunoglobulin heavy (IGH) gene locus of the Brown Norway (BN) rat
(assembly V3.4; Rat Genomic Sequence Consortium). In addition to known variable region genes, we found 12 novel previously
unidentified functional IGHV genes and 1 novel functional IGHD gene. In total, the variable region of the rat IGH locus is composed of at least 353 unique IGHV genes, 21 IGHD genes, and 5 IGHJ genes, of which 131, 14, and 4 are potentially functional genes, respectively. Of all species studied so far, the rat seems
to have the highest number of functional IGHV genes in the genome. Rat IGHV genes can be classified into 13 IGHV families based on nucleotide sequence identity. The variable region of the BN rat spans
a total length of approximately 4.9 Mb and is organized in a typical translocon organization. Like the mouse, members of the
various IGHV gene families are more or less grouped together on the genome, albeit some members of IGHV gene families are
found intermingled with each other. In the rat, the largest IGHV gene families are IGHV1, IGHV2, and IGHV5. The overall conclusion
is that the genomic organization of the variable region of the rat IGH locus is strikingly similar to that of the mouse, illustrating
the close evolutionary relationship between these two species. 相似文献
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FIT是调控拟南芥铁稳态的一个关键调控因子,它在转录水平上受到缺铁诱导,但其背后的调控机制还不甚清楚。该研究以拟南芥bHLH38和FIT的单、双过表达植物及bHLH Ib四突变体植物为材料,采用缺铁(-Fe)处理实验和定量RT-PCR的方法从RNA角度分析了FIT转录水平的变化。结果表明:(1)在铁充足时,bHLH38过表达植物中FIT的转录水平显著高于其在野生型中的水平。(2)在bHLH Ib四突变体植物中FIT的转录水平不受缺铁诱导。(3)FIT单过表达不能激活内源FIT的转录,而在加铁(+Fe)条件下bHLH38和FIT的双过表达则可以激活内源FIT的转录。(4)在缺铁条件下,所有植物中FIT的转录水平均与野生型中的FIT水平无明显差异。基于以上结果认为,bHLH Ib转录因子是缺铁诱导FIT转录的必要条件,而非充分条件。该研究结果为深入了解植物通过多种途径共同维持铁稳态提供了新的见解。 相似文献
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Roger S. Holmes Matthew W. Wright Stanley J. F. Laulederkind Laura A. Cox Masakiyo Hosokawa Teruko Imai Shun Ishibashi Richard Lehner Masao Miyazaki Everett J. Perkins Phillip M. Potter Matthew R. Redinbo Jacques Robert Tetsuo Satoh Tetsuro Yamashita Bingfan Yan Tsuyoshi Yokoi Rudolf Zechner Lois J. Maltais 《Mammalian genome》2010,21(9-10):427-441
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