Literature DB >> 17156942

The evolution of High Mobility Group Box (HMGB) chromatin proteins in multicellular animals.

Luca Sessa1, Marco E Bianchi.   

Abstract

Mammalian HMGB proteins are abundant chromatin components, and are characterized by the presence of 2 HMG-box domains and an acidic tail. HMG boxes are present in a large number of DNA-binding proteins, and HMGB chromatin proteins represent a small and specific subset of HMG-box proteins. The comparison of DNA sequences that code for HMG-box proteins suggests that the ancestral HMG box was coded by an intronless gene, which picked up one or more introns during its radiation. Canonical HMGB proteins are only present in multicellular animals, from sponges onwards, and appear to have arisen through the fusion of two different genes, each coding for one of the boxes. The organization of HMGB genes was very conserved during Metazoan evolution, with the only deviations appearing in Caenorhabditis and Dipteran (Drosophila and Anopheles) species.

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Year:  2006        PMID: 17156942     DOI: 10.1016/j.gene.2006.08.034

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  24 in total

1.  Systematic identification of gene activities promoting hypoxic death.

Authors:  Meghann E Mabon; Xianrong Mao; York Jiao; Barbara A Scott; C Michael Crowder
Journal:  Genetics       Date:  2008-12-01       Impact factor: 4.562

Review 2.  High mobility group proteins and their post-translational modifications.

Authors:  Qingchun Zhang; Yinsheng Wang
Journal:  Biochim Biophys Acta       Date:  2008-05-10

3.  Dynamic localization and the associated translocation mechanism of HMGBs in response to GCRV challenge in CIK cells.

Authors:  Youliang Rao; Jianguo Su; Chunrong Yang; Nana Yan; Xiaohui Chen; Xiaoli Feng
Journal:  Cell Mol Immunol       Date:  2014-07-21       Impact factor: 11.530

4.  Uterine deficiency of high-mobility group box-1 (HMGB1) protein causes implantation defects and adverse pregnancy outcomes.

Authors:  Shizu Aikawa; Wenbo Deng; Xiaohuan Liang; Jia Yuan; Amanda Bartos; Xiaofei Sun; Sudhansu K Dey
Journal:  Cell Death Differ       Date:  2019-10-08       Impact factor: 15.828

5.  HMGB factors are required for posterior digit development through integrating signaling pathway activities.

Authors:  Junji Itou; Noboru Taniguchi; Isao Oishi; Hiroko Kawakami; Martin Lotz; Yasuhiko Kawakami
Journal:  Dev Dyn       Date:  2011-03-07       Impact factor: 3.780

Review 6.  The Fatal Circle of NETs and NET-Associated DAMPs Contributing to Organ Dysfunction.

Authors:  Helena Block; Jan Rossaint; Alexander Zarbock
Journal:  Cells       Date:  2022-06-14       Impact factor: 7.666

7.  HMGB1 protein does not mediate the inflammatory response in spontaneous spinal cord regeneration: a hint for CNS regeneration.

Authors:  Yingying Dong; Yun Gu; Youjuan Huan; Yingjie Wang; Yan Liu; Mei Liu; Fei Ding; Xiaosong Gu; Yongjun Wang
Journal:  J Biol Chem       Date:  2013-05-06       Impact factor: 5.157

8.  Anti-HMGB1 auto-Abs influence fatigue in patients with Crohn's disease.

Authors:  Ingeborg Kvivik; Tore Grimstad; Grete Jonsson; Jan T Kvaløy; Roald Omdal
Journal:  Innate Immun       Date:  2021-05-03       Impact factor: 2.680

Review 9.  RAGE (Receptor for Advanced Glycation Endproducts), RAGE ligands, and their role in cancer and inflammation.

Authors:  Louis J Sparvero; Denise Asafu-Adjei; Rui Kang; Daolin Tang; Neilay Amin; Jaehyun Im; Ronnye Rutledge; Brenda Lin; Andrew A Amoscato; Herbert J Zeh; Michael T Lotze
Journal:  J Transl Med       Date:  2009-03-17       Impact factor: 5.531

10.  Redox modifications of cysteine residues regulate the cytokine activity of HMGB1.

Authors:  Huan Yang; Peter Lundbäck; Lars Ottosson; Helena Erlandsson-Harris; Emilie Venereau; Marco E Bianchi; Yousef Al-Abed; Ulf Andersson; Kevin J Tracey
Journal:  Mol Med       Date:  2021-06-07       Impact factor: 6.354

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