Matches in SemOpenAlex for { <https://semopenalex.org/work/W2049156612> ?p ?o ?g. }
- W2049156612 endingPage "177" @default.
- W2049156612 startingPage "167" @default.
- W2049156612 abstract "Following a previous isolation by reverse-phase HPLC of five histone H1 subtypes from adult rat liver, purity of three of them, H1a, H1b and H1d (according to Lennox's nomenclature), was achieved. Structural features of these three subtypes were investigated. Partial cleavage of these subtypes by endoproteinase Glu-C showed a different behavior of the H1a subtype when compared to the H1b and H1d subtypes. Under the conditions used in this work, the H1b and H1d subtypes present three major sites accessible to the endoproteinase Glu-C, while the H1a subtype presents only one major site accessible to the proteinase. Partial N-terminal sequence of the different fragments obtained after proteolysis indicated that the two H1b and H1d subtypes were cleaved inside the globular domain (Glu-54,-75) and between the globular domain and the C-terminal one (Glu-116). The H1a subtype was only cleaved between the globular domain and the C-terminal tail (Glu-116), though Glu-54 and Glu-75 sites were present. These results would suggest some differences in the conformation of these proteins. Furthermore, the partial determined sequences of H1b showed 85% similarity to each other (the main differences were threonine residues instead of alanine residues in the C-terminal domain) while H1a was only 60% similar to H1b and H1d, for the sequences which aligned. The strongest differences between the H1a subtype and the two other subtypes were observed in the first amino acid residues of the C-terminal domain. The 117–126 amino acid residues (SKASTTKVTV) of H1a were quite different from those of H1b and H1d. This sequence, which showed a number of serine and threonine residues, was not found in any other histone sequence, after consultation with data bases. This H1a subtype was a minor component in adult liver (2.4%). As it was described in testis as a major component, testis histone H1 proteins were fractionated onto reverse-phase HPLC under the same conditions as those used for histone H1 proteins from liver. The pure testis H1a fraction was submitted to the endoproteinase Glu-C digestion. The pattern digestion was the same as that observed for liver H1a. The two 44–76 and 117–126 determined amino acid residues of H1a from testis were strictly identical to those of liver H1a. We demonstrate that H1a is the same protein in liver and testis and we give evidence for a specific motif SKASTTKVTV (117–126 residues) in the sequence of the C-terminal domain. The refolding of the three liver subtypes H1a, H1b and H1d and the testis H1a was followed by CD measurements. H1d presented 10.5% of α helix. H1a and H1b showed 12.5 and 13.4% of α helix. H1a from liver and testis presented a similar α helix percentage. The involvement of all these structural differences in physiological functions of the H1a subtype is discussed." @default.
- W2049156612 created "2016-06-24" @default.
- W2049156612 creator A5012539361 @default.
- W2049156612 creator A5054967022 @default.
- W2049156612 creator A5076187430 @default.
- W2049156612 creator A5090983324 @default.
- W2049156612 date "1992-07-01" @default.
- W2049156612 modified "2023-09-25" @default.
- W2049156612 title "Histone H1a subtype presents structural differences compared to other histone H1 subtypes. Evidence for a specific motif in the C-terminal domain" @default.
- W2049156612 cites W1486348319 @default.
- W2049156612 cites W1499182986 @default.
- W2049156612 cites W1500224677 @default.
- W2049156612 cites W1520024145 @default.
- W2049156612 cites W1533155803 @default.
- W2049156612 cites W1539870587 @default.
- W2049156612 cites W1542748993 @default.
- W2049156612 cites W1559554438 @default.
- W2049156612 cites W1575311161 @default.
- W2049156612 cites W1607032234 @default.
- W2049156612 cites W1621414326 @default.
- W2049156612 cites W1630449726 @default.
- W2049156612 cites W1841613381 @default.
- W2049156612 cites W1859417845 @default.
- W2049156612 cites W1951806016 @default.
- W2049156612 cites W1968802467 @default.
- W2049156612 cites W1978896972 @default.
- W2049156612 cites W1985584427 @default.
- W2049156612 cites W1987907616 @default.
- W2049156612 cites W1997419979 @default.
- W2049156612 cites W1999485774 @default.
- W2049156612 cites W2005637685 @default.
- W2049156612 cites W2012635848 @default.
- W2049156612 cites W2012755542 @default.
- W2049156612 cites W2014550271 @default.
- W2049156612 cites W2015761344 @default.
- W2049156612 cites W2016922286 @default.
- W2049156612 cites W2027328719 @default.
- W2049156612 cites W2028895755 @default.
- W2049156612 cites W2031236107 @default.
- W2049156612 cites W2046920177 @default.
- W2049156612 cites W2051304379 @default.
- W2049156612 cites W2057823932 @default.
- W2049156612 cites W2058958205 @default.
- W2049156612 cites W2060676190 @default.
- W2049156612 cites W2065897406 @default.
- W2049156612 cites W2067747620 @default.
- W2049156612 cites W2077130049 @default.
- W2049156612 cites W2077844535 @default.
- W2049156612 cites W2079314213 @default.
- W2049156612 cites W2080035645 @default.
- W2049156612 cites W2082497364 @default.
- W2049156612 cites W2083939800 @default.
- W2049156612 cites W2090819627 @default.
- W2049156612 cites W2100837269 @default.
- W2049156612 cites W2114869918 @default.
- W2049156612 cites W2148347504 @default.
- W2049156612 cites W2179190216 @default.
- W2049156612 cites W2190983879 @default.
- W2049156612 cites W2205018925 @default.
- W2049156612 cites W2311219659 @default.
- W2049156612 cites W2344397152 @default.
- W2049156612 cites W247725554 @default.
- W2049156612 doi "https://doi.org/10.1016/0167-4838(92)90320-d" @default.
- W2049156612 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/1643090" @default.
- W2049156612 hasPublicationYear "1992" @default.
- W2049156612 type Work @default.
- W2049156612 sameAs 2049156612 @default.
- W2049156612 citedByCount "3" @default.
- W2049156612 crossrefType "journal-article" @default.
- W2049156612 hasAuthorship W2049156612A5012539361 @default.
- W2049156612 hasAuthorship W2049156612A5054967022 @default.
- W2049156612 hasAuthorship W2049156612A5076187430 @default.
- W2049156612 hasAuthorship W2049156612A5090983324 @default.
- W2049156612 hasConcept C104317684 @default.
- W2049156612 hasConcept C105168689 @default.
- W2049156612 hasConcept C119157956 @default.
- W2049156612 hasConcept C151730666 @default.
- W2049156612 hasConcept C167625842 @default.
- W2049156612 hasConcept C175156509 @default.
- W2049156612 hasConcept C181199279 @default.
- W2049156612 hasConcept C185592680 @default.
- W2049156612 hasConcept C2775880066 @default.
- W2049156612 hasConcept C2776016237 @default.
- W2049156612 hasConcept C2776414213 @default.
- W2049156612 hasConcept C2779856020 @default.
- W2049156612 hasConcept C2781307694 @default.
- W2049156612 hasConcept C43369102 @default.
- W2049156612 hasConcept C515207424 @default.
- W2049156612 hasConcept C552990157 @default.
- W2049156612 hasConcept C55493867 @default.
- W2049156612 hasConcept C57711820 @default.
- W2049156612 hasConcept C64927066 @default.
- W2049156612 hasConcept C86803240 @default.
- W2049156612 hasConceptScore W2049156612C104317684 @default.
- W2049156612 hasConceptScore W2049156612C105168689 @default.
- W2049156612 hasConceptScore W2049156612C119157956 @default.
- W2049156612 hasConceptScore W2049156612C151730666 @default.
- W2049156612 hasConceptScore W2049156612C167625842 @default.