Intrinsically unstructured proteins evolve by repeat expansion

被引:225
|
作者
Tompa, P [1 ]
机构
[1] Hungarian Acad Sci, Biol Res Ctr, Inst Enzymol, H-1518 Budapest, Hungary
关键词
D O I
10.1002/bies.10324
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The proportion of the genome encoding intrinsically unstructured proteins increases with the complexity of organisms, which demands specific mechanism(s) for generating novel genetic material of this sort. Here it is suggested that one such mechanism is the expansion of internal repeat regions, i.e., coding micro- and minisatellites. An analysis of 126 known unstructured sequences shows the preponderance of repeats: the percentage of proteins with tandemly repeated short segments is much higher in this class (39%) than earlier reported for all Swiss-Prot (14%), yeast (18%) or human (28%) proteins. Furthermore, prime examples, such as salivary proline-rich proteins, titin, eukaryotic RNA polymerase II, the prion protein and several others, demonstrate that the repetitive segments carry fundamental function in these proteins. In addition, their repeat numbers show functionally significant interspecies variation and polymorphism, which underlines that these regions have been shaped by intense evolutionary activity. In all, the major point of this paper is that the genetic instability of repetitive regions combined with the structurally and functionally permissive nature of unstructured proteins has powered the extension and possible functional expansion of this newly recognized proteinclass. (C) 2003 Wiley Periodicals, Inc.
引用
收藏
页码:847 / 855
页数:9
相关论文
共 50 条
  • [41] Conformational modulation mediated by polyglutamine expansion in CAG repeat expansion disease-associated proteins
    Verani, Margherita
    Bustamante, Maria
    Martufi, Paola
    Daldin, Manuel
    Cariulo, Cristina
    Azzollini, Lucia
    Fodale, Valentina
    Puglisi, Francesca
    Weiss, Andreas
    Macdonald, Douglas
    Petricca, Lara
    Caricasole, Andrea
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2016, 478 (02) : 949 - 955
  • [42] Intrinsically disordered proteins and proteins with intrinsically disordered regions in neurodegenerative diseases
    Orkid Coskuner-Weber
    Ozan Mirzanli
    Vladimir N. Uversky
    Biophysical Reviews, 2022, 14 : 679 - 707
  • [43] Therapeutic targeting of mismatch repair proteins in triplet repeat expansion diseases
    Marzec, Paulina
    Richer, Madeleine
    Lahue, Robert S.
    DNA REPAIR, 2025, 147
  • [44] Expansion and Function of Repeat Domain Proteins During Stress and Development in Plants
    Sharma, Manisha
    Pandey, Girdhar K.
    FRONTIERS IN PLANT SCIENCE, 2016, 6
  • [45] The pairwise energy content estimated from amino acid composition discriminates between folded and intrinsically unstructured proteins
    Dosztányi, Z
    Csizmók, V
    Tompa, P
    Simon, I
    JOURNAL OF MOLECULAR BIOLOGY, 2005, 347 (04) : 827 - 839
  • [46] The pairwise energy content estimated from amino acid composition discriminates between folded and intrinsically unstructured proteins
    Dosztanyi, Z
    Csizmok, V
    Tompa, P
    Simon, I
    FEBS JOURNAL, 2005, 272 : 360 - 360
  • [47] Mapping Unstructured Regions and Synergistic Folding in Intrinsically Disordered Proteins with Amide H/D Exchange Mass Spectrometry
    Keppel, Theodore R.
    Howard, Brent A.
    Weis, David D.
    BIOCHEMISTRY, 2011, 50 (40) : 8722 - 8732
  • [48] A new strategy for sequential assignment of intrinsically unstructured proteins based on 15N single isotope labelling
    Lopez, Juan
    Ahuja, Puneet
    Gerard, Melanie
    Wieruszeski, Jean-Michel
    Lippens, Guy
    JOURNAL OF MAGNETIC RESONANCE, 2013, 236 : 1 - 6
  • [49] Intrinsically disordered proteins
    Dunker, A. K.
    Uversky, V. N.
    Oldfield, C. J.
    Mohan, A.
    Cheng, Y.
    Zaidi, S.
    Romero, P. R.
    Xie, H.
    Obradovic, Z.
    BIOPHYSICAL JOURNAL, 2007, : 1A - 1A
  • [50] Quantifying Disorder of an Intrinsically Unstructured Domain in Estrogen Receptor
    Peng, Yi
    Cao, Shufen
    Buck, Matthias
    Yang, Sichun
    BIOPHYSICAL JOURNAL, 2018, 114 (03) : 428A - 428A