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<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{Infobox_gene}}
{{PBB_Controls
'''Histone RNA hairpin-binding protein''' or '''stem-loop binding protein''' (SLBP) is a [[protein]] that in humans is encoded by the ''SLBP'' [[gene]].<ref name="pmid9049306">{{cite journal | vauthors = Martin F, Schaller A, Eglite S, Schumperli D, Muller B | title = The gene for histone RNA hairpin binding protein is located on human chromosome 4 and encodes a novel type of RNA binding protein | journal = EMBO J | volume = 16 | issue = 4 | pages = 769–78 |date=Mar 1997 | pmid = 9049306 | pmc = 1169678 | doi = 10.1093/emboj/16.4.769 }}</ref><ref name="pmid1338771">{{cite journal | vauthors = McCombie WR, Martin-Gallardo A, Gocayne JD, FitzGerald M, Dubnick M, Kelley JM, Castilla L, Liu LI, Wallace S, Trapp S | title = Expressed genes, Alu repeats and polymorphisms in cosmids sequenced from chromosome 4p16.3 | journal = Nature Genetics | volume = 1 | issue = 5 | pages = 348–53 |date=August 1992 | pmid = 1338771 | doi = 10.1038/ng0892-348 | url = }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: SLBP stem-loop (histone) binding protein| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7884| accessdate = }}</ref>
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
}}


<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
== Species distribution ==
{{GNF_Protein_box
| image =
| image_source =
| PDB =  
| Name = Stem-loop (histone) binding protein
| HGNCid = 10904
| Symbol = SLBP
| AltSymbols =; HBP
| OMIM = 602422
| ECnumber = 
| Homologene = 31389
| MGIid = 108402
| GeneAtlas_image1 = PBB_GE_SLBP_206052_s_at_tn.png
| Function = {{GNF_GO|id=GO:0003729 |text = mRNA binding}}
| Component = {{GNF_GO|id=GO:0005634 |text = nucleus}} {{GNF_GO|id=GO:0030529 |text = ribonucleoprotein complex}}
| Process = {{GNF_GO|id=GO:0006397 |text = mRNA processing}} {{GNF_GO|id=GO:0006398 |text = histone mRNA 3'-end processing}}
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 7884
    | Hs_Ensembl = ENSG00000163950
    | Hs_RefseqProtein = NP_006518
    | Hs_RefseqmRNA = NM_006527
    | Hs_GenLoc_db = 
    | Hs_GenLoc_chr = 4
    | Hs_GenLoc_start = 1664325
    | Hs_GenLoc_end = 1684080
    | Hs_Uniprot = Q14493
    | Mm_EntrezGene = 20492
    | Mm_Ensembl = ENSMUSG00000004642
    | Mm_RefseqmRNA = NM_009193
    | Mm_RefseqProtein = NP_033219
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = 5
    | Mm_GenLoc_start = 33951991
    | Mm_GenLoc_end = 33969166
    | Mm_Uniprot = Q3TSD8
  }}
}}
'''Stem-loop (histone) binding protein''', also known as '''SLBP''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: SLBP stem-loop (histone) binding protein| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7884| accessdate = }}</ref>


<!-- The PBB_Summary template is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
SLBP has been cloned from humans,  ''[[Caenorhabditis elegans|C. elegans]]'', ''[[Drosophila melanogaster|D. melanogaster]]'', ''[[African clawed frog|X. laevis]]'', and [[sea urchins]].  The full length human protein has 270 amino acids (31 kDa) with a centrally located RNA binding domain (RBD).  The 75 amino acid RBD is well conserved across species, however the remainder of SLBP is highly divergent in most organisms and not homologous to any other protein in the eukaryotic genomes.
{{PBB_Summary
 
| section_title =  
== Function ==
| summary_text = This gene encodes a protein that binds to the stem-loop structure in replication-dependent histone mRNAs. Histone mRNAs do not contain introns or polyadenylation signals, and are processed by endonucleolytic cleavage. The stem-loop structure is essential for efficient processing but this structure also controls the transport, translation and stability of histone mRNAs. Expression of the protein is regulated during the cell cycle, increasing more than 10-fold during the latter part of G1.<ref name="entrez">{{cite web | title = Entrez Gene: SLBP stem-loop (histone) binding protein| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7884| accessdate = }}</ref>
This gene encodes a [[protein]] that binds to the [[histone 3' UTR stem-loop]] structure in [[DNA replication|replication]]-dependent [[histone]] [[messenger RNA|mRNAs]]. Histone mRNAs do not contain [[introns]] or [[polyadenylation]] signals, and are processed by a single [[endonuclease|endonucleolytic]] cleavage event downstream of the stem-loop. The stem-loop structure is essential for efficient processing of the histone pre-mRNA but this structure also controls the transport, [[translation (biology)|translation]] and stability of histone mRNAs. SLBP [[gene expression|expression]] is regulated during S-phase of the [[cell cycle]], increasing more than 10-fold during the latter part of [[G1 phase|G1]].
}}
 
All SLBP proteins are capable of forming a highly stable complex with histone stem-loop RNA. Complex formation with the histone mRNA stem-loop is achieved by a novel three-helix bundle fold.  SLBP proteins also recognize the tetraloop structure of the histone hairpin, the base of the stem, and the 5' flanking region. The crystal structure of human SLBP in complex with the stem-loop RNA as well as the [[exonuclease]] [[Eri1]] reveals that the Arg181 residue of SLBP specifically interacts with the second [[guanine]] base in the RNA stem.<ref name="pmid23329046">{{cite journal | author = Dazhi Tan | author2 = William F. Marzluff | author3 = Zbigniew Dominski | author4 = Liang Tong | title = Structure of Histone mRNA Stem-Loop, Human Stem-Loop Binding Protein, and 3′hExo Ternary Complex | journal = Science | volume = 339 | issue = 6117 | pages = 318–321 |date=Jan 2013 | pmid = 23329046 | doi = 10.1126/science.1228705 | pmc=3552377}}</ref> The rest of the protein is intrinsically disordered in fruit-flies as well as in humans.  A unique feature of the SLBP RBD is that it is [[phosphorylated]] in its RNA binding domain at the Thr171 residue. The SLBP RBD also undergoes proline isomerization about this sequence and is a substrate for the prolyl isomerase Pin1.  The [[N-terminal]] domain of human SLBP is required for translation activation of histone mRNAs via its interaction with SLIP1.  SLBP also interacts with the CBP80 associated protein CTIF to facilitate rapid degradation of histone mRNAs.  SLBP is a phosphoprotein and besides T171, it is also phosphorylated at Ser7, Ser20, Ser23, Thr60, Thr61 in mammalian cells.  The phosphorylation at Thr60 is mediated by CK2 and Thr61 is by [[Cyclin A]]/[[Cdk1]].<ref name="entrez" />


==References==
==References==
{{reflist|2}}
{{reflist}}
 
==Further reading==
==Further reading==
{{refbegin | 2}}
{{refbegin | 2}}
{{PBB_Further_reading
* {{cite journal | vauthors = Choe J, Mi Kim K, Park S, Kyung Lee Y, ((Song O-K)), Kim MK, Lee BG, Song HK, Kim YK | title = Rapid degradation of replication-dependent histone mRNAs largely occurs on mRNAs bound by nuclear cap-binding proteins 80 and 20 | journal = Nucleic Acids Research |  year = 2013 | volume = 41 | issue = 2 | pages = 1307–1318 | doi = 10.1093/nar/gks1196 }}
| citations =
* {{cite journal | vauthors = Bansal N, Zhang M, Bhaskar A, Itotia P, Lee E, Shlyakhtenko LS, Lam TT, Fritz A, Berezney R, Lyubchenko YL, Stafford WF, Thapar R | title = Assembly of the SLIP1-SLBP complex on histone mRNA requires heterodimerization and sequential binding of SLBP followed by SLIP1 | journal = Biochemistry |date=January 2013 | volume = 52 | issue = 3 | pages = 520–536 | doi = 10.1021/bi301074r | pmid=23286197 | pmc=3580866}}
*{{cite journal | author=McCombie WR, Martin-Gallardo A, Gocayne JD, ''et al.'' |title=Expressed genes, Alu repeats and polymorphisms in cosmids sequenced from chromosome 4p16.3. |journal=Nat. Genet. |volume=1 |issue= 5 |pages= 348-53 |year= 1993 |pmid= 1338771 |doi= 10.1038/ng0892-348 }}
* {{cite journal | vauthors = Martin L, Meier M, Lyons SM, Sit RV, Marzluff WF, Quake SR, Chang HY |authorlink7=Howard Y. Chang| title = Systematic reconstruction of RNA functional motifs with high-throughput microfluidics | journal = Nature Methods | volume = 9 | issue = 12 | pages = 1192–4 |date=December 2012 | doi = 10.1038/nmeth.2225 | pmc = 3863600 }}
*{{cite journal | author=Hanson RJ, Sun J, Willis DG, Marzluff WF |title=Efficient extraction and partial purification of the polyribosome-associated stem-loop binding protein bound to the 3' end of histone mRNA. |journal=Biochemistry |volume=35 |issue= 7 |pages= 2146-56 |year= 1996 |pmid= 8652556 |doi= 10.1021/bi9521856 }}
* {{cite journal | vauthors = Krishnan N, Lam TT, Fritz A, Rempinski D, O'Loughlin K, Minderman H, Berezney R, Marzluff WF, Thapar R | title = The Prolyl Isomerase Pin1 Targets Stem-Loop Binding Protein (SLBP) To Dissociate the SLBP-Histone mRNA Complex Linking Histone mRNA Decay with SLBP Ubiquitination | journal = Mol. Cell. Biol. | volume = 32 | issue = 21 | pages = 4306–22 |date=November 2012 | pmid = 22907757 | doi = 10.1128/MCB.00382-12 | pmc = 3486140 }}
*{{cite journal | author=Wang ZF, Whitfield ML, Ingledue TC, ''et al.'' |title=The protein that binds the 3' end of histone mRNA: a novel RNA-binding protein required for histone pre-mRNA processing. |journal=Genes Dev. |volume=10 |issue= 23 |pages= 3028-40 |year= 1997 |pmid= 8957003 |doi= }}
* {{cite journal | vauthors = Zhang M, Lam TT, Tonelli M, Marzluff WF, Thapar R | title = Interaction of the histone mRNA hairpin with stem-loop binding protein (SLBP) and regulation of the SLBP-RNA complex by phosphorylation and proline isomerization | journal = Biochemistry | volume = 51 | issue = 15 | pages = 3215–31 |date=April 2012 | pmid = 22439849 | doi = 10.1021/bi2018255 | pmc = 3328597 }}
*{{cite journal | author=Martin F, Schaller A, Eglite S, ''et al.'' |title=The gene for histone RNA hairpin binding protein is located on human chromosome 4 and encodes a novel type of RNA binding protein. |journal=EMBO J. |volume=16 |issue= 4 |pages= 769-78 |year= 1997 |pmid= 9049306 |doi= 10.1093/emboj/16.4.769 }}
* {{cite journal | vauthors = Borchers CH, Thapar R, Petrotchenko EV, Torres MP, Speir JP, Easterling M, Dominski Z, Marzluff WF | title = Combined top-down and bottom-up proteomics identifies a phosphorylation site in stem-loop-binding proteins that contributes to high-affinity RNA binding | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 103 | issue = 9 | pages = 3094–9 |date=February 2006 | pmid = 16492733 | pmc = 1413926 | doi = 10.1073/pnas.0511289103 }}
*{{cite journal | author=Dominski Z, Zheng LX, Sanchez R, Marzluff WF |title=Stem-loop binding protein facilitates 3'-end formation by stabilizing U7 snRNP binding to histone pre-mRNA. |journal=Mol. Cell. Biol. |volume=19 |issue= 5 |pages= 3561-70 |year= 1999 |pmid= 10207079 |doi= }}
* {{cite journal | vauthors = Thapar R, Marzluff WF, Redinbo MR | title = Electrostatic contribution of serine phosphorylation to the Drosophila SLBP--histone mRNA complex | journal = Biochemistry | volume = 43 | issue = 29 | pages = 9401–12 |date=July 2004 | pmid = 15260483 | doi = 10.1021/bi036315j }}
*{{cite journal | author=Whitfield ML, Zheng LX, Baldwin A, ''et al.'' |title=Stem-loop binding protein, the protein that binds the 3' end of histone mRNA, is cell cycle regulated by both translational and posttranslational mechanisms. |journal=Mol. Cell. Biol. |volume=20 |issue= 12 |pages= 4188-98 |year= 2000 |pmid= 10825184 |doi= }}
* {{cite journal | vauthors = Thapar R, Mueller GA, Marzluff WF | title = The N-terminal domain of the Drosophila histone mRNA binding protein, SLBP, is intrinsically disordered with nascent helical structure | journal = Biochemistry | volume = 43 | issue = 29 | pages = 9390–400 |date=July 2004 | pmid = 15260482 | doi = 10.1021/bi036314r }}
*{{cite journal | author=Kato M, Miyazawa K, Kitamura N |title=A deubiquitinating enzyme UBPY interacts with the Src homology 3 domain of Hrs-binding protein via a novel binding motif PX(V/I)(D/N)RXXKP. |journal=J. Biol. Chem. |volume=275 |issue= 48 |pages= 37481-7 |year= 2001 |pmid= 10982817 |doi= 10.1074/jbc.M007251200 }}
* {{cite journal | vauthors = Wang ZF, Whitfield ML, Ingledue TC, Dominski Z, Marzluff WF | title = The protein that binds the 3' end of histone mRNA: a novel RNA-binding protein required for histone pre-mRNA processing | journal = Genes Dev. | volume = 10 | issue = 23 | pages = 3028–40 |date=December 1996 | pmid = 8957003 | doi = 10.1101/gad.10.23.3028  }}
*{{cite journal | author=Dominski Z, Erkmann JA, Greenland JA, Marzluff WF |title=Mutations in the RNA binding domain of stem-loop binding protein define separable requirements for RNA binding and for histone pre-mRNA processing. |journal=Mol. Cell. Biol. |volume=21 |issue= 6 |pages= 2008-17 |year= 2001 |pmid= 11238936 |doi= 10.1128/MCB.21.6.2008-2017.2001 }}
* {{cite journal | vauthors = Dominski Z, Zheng LX, Sanchez R, Marzluff WF | title = Stem-loop binding protein facilitates 3'-end formation by stabilizing U7 snRNP binding to histone pre-mRNA | journal = Mol. Cell. Biol. | volume = 19 | issue = 5 | pages = 3561–70 |date=May 1999 | pmid = 10207079 | pmc = 84148 | doi = 10.1128/mcb.19.5.3561}}
*{{cite journal | author=Dominski Z, Erkmann JA, Yang X, ''et al.'' |title=A novel zinc finger protein is associated with U7 snRNP and interacts with the stem-loop binding protein in the histone pre-mRNP to stimulate 3'-end processing. |journal=Genes Dev. |volume=16 |issue= 1 |pages= 58-71 |year= 2002 |pmid= 11782445 |doi= 10.1101/gad.932302 }}
* {{cite journal | vauthors = Whitfield ML, Zheng LX, Baldwin A, Ohta T, Hurt MM, Marzluff WF | title = Stem-loop binding protein, the protein that binds the 3' end of histone mRNA, is cell cycle regulated by both translational and posttranslational mechanisms | journal = Mol. Cell. Biol. | volume = 20 | issue = 12 | pages = 4188–98 |date=June 2000 | pmid = 10825184 | pmc = 85788 | doi = 10.1128/MCB.20.12.4188-4198.2000 }}
*{{cite journal | author=Allard P, Champigny MJ, Skoggard S, ''et al.'' |title=Stem-loop binding protein accumulates during oocyte maturation and is not cell-cycle-regulated in the early mouse embryo. |journal=J. Cell. Sci. |volume=115 |issue= Pt 23 |pages= 4577-86 |year= 2003 |pmid= 12415002 |doi= }}
* {{cite journal | vauthors = Dominski Z, Erkmann JA, Greenland JA, Marzluff WF | title = Mutations in the RNA binding domain of stem-loop binding protein define separable requirements for RNA binding and for histone pre-mRNA processing | journal = Mol. Cell. Biol. | volume = 21 | issue = 6 | pages = 2008–17 |date=March 2001 | pmid = 11238936 | pmc = 86798 | doi = 10.1128/MCB.21.6.2008-2017.2001 }}
*{{cite journal | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899-903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 }}
* {{cite journal | vauthors = Allard P, Champigny MJ, Skoggard S, Erkmann JA, Whitfield ML, Marzluff WF, Clarke HJ | title = Stem-loop binding protein accumulates during oocyte maturation and is not cell-cycle-regulated in the early mouse embryo | journal = J. Cell Sci. | volume = 115 | issue = Pt 23 | pages = 4577–86 |date=December 2002 | pmid = 12415002 | doi = 10.1242/jcs.00132 }}
*{{cite journal | author=Zheng L, Dominski Z, Yang XC, ''et al.'' |title=Phosphorylation of stem-loop binding protein (SLBP) on two threonines triggers degradation of SLBP, the sole cell cycle-regulated factor required for regulation of histone mRNA processing, at the end of S phase. |journal=Mol. Cell. Biol. |volume=23 |issue= 5 |pages= 1590-601 |year= 2003 |pmid= 12588979 |doi= }}
* {{cite journal | vauthors = Zheng L, Dominski Z, Yang XC, Elms P, Raska CS, Borchers CH, Marzluff WF | title = Phosphorylation of stem-loop binding protein (SLBP) on two threonines triggers degradation of SLBP, the sole cell cycle-regulated factor required for regulation of histone mRNA processing, at the end of S phase | journal = Mol. Cell. Biol. | volume = 23 | issue = 5 | pages = 1590–601 |date=March 2003 | pmid = 12588979 | pmc = 151715 | doi = 10.1128/MCB.23.5.1590-1601.2003 }}
*{{cite journal | author=Dominski Z, Yang XC, Kaygun H, ''et al.'' |title=A 3' exonuclease that specifically interacts with the 3' end of histone mRNA. |journal=Mol. Cell |volume=12 |issue= 2 |pages= 295-305 |year= 2003 |pmid= 14536070 |doi= }}
* {{cite journal | vauthors = Koseoglu MM, Graves LM, Marzluff WF | title = Phosphorylation of threonine 61 by cyclin a/Cdk1 triggers degradation of stem-loop binding protein at the end of S phase | journal = Mol. Cell. Biol. | volume = 28 | issue = 14 | pages = 4469–79 |date=July 2008 | pmid = 18490441 | pmc = 2447125 | doi = 10.1128/MCB.01416-07 }}
*{{cite journal | author=Ota T, Suzuki Y, Nishikawa T, ''et al.'' |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40-5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}
* {{cite journal | vauthors = Sànchez R, Marzluff WF | title = The stem-loop binding protein is required for efficient translation of histone mRNA in vivo and in vitro | journal = Mol. Cell. Biol. | volume = 22 | issue = 20 | pages = 7093–104 |date=October 2002 | pmid = 12242288 | pmc = 139811 | doi = 10.1128/mcb.22.20.7093-7104.2002}}
*{{cite journal | author=Gerhard DS, Wagner L, Feingold EA, ''et al.'' |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121-7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 }}
* {{cite journal | vauthors = Zhao X, McKillop-Smith S, Müller B | title = The human histone gene expression regulator HBP/SLBP is required for histone and DNA synthesis, cell cycle progression and cell proliferation in mitotic cells | journal = J. Cell Sci. | volume = 117 | issue = Pt 25 | pages = 6043–51 |date=December 2004 | pmid = 15546920 | doi = 10.1242/jcs.01523 }}
*{{cite journal | author=Zhao X, McKillop-Smith S, Müller B |title=The human histone gene expression regulator HBP/SLBP is required for histone and DNA synthesis, cell cycle progression and cell proliferation in mitotic cells. |journal=J. Cell. Sci. |volume=117 |issue= Pt 25 |pages= 6043-51 |year= 2005 |pmid= 15546920 |doi= 10.1242/jcs.01523 }}
* {{cite journal | vauthors = Erkmann JA, Wagner EJ, Dong J, Zhang Y, Kutay U, Marzluff WF | title = Nuclear import of the stem-loop binding protein and localization during the cell cycle | journal = Mol. Biol. Cell | volume = 16 | issue = 6 | pages = 2960–71 |date=June 2005 | pmid = 15829567 | pmc = 1142439 | doi = 10.1091/mbc.E04-11-1023 }}
*{{cite journal | author=Erkmann JA, Wagner EJ, Dong J, ''et al.'' |title=Nuclear import of the stem-loop binding protein and localization during the cell cycle. |journal=Mol. Biol. Cell |volume=16 |issue= 6 |pages= 2960-71 |year= 2005 |pmid= 15829567 |doi= 10.1091/mbc.E04-11-1023 }}
*{{cite journal | author=Wagner EJ, Berkow A, Marzluff WF |title=Expression of an RNAi-resistant SLBP restores proper S-phase progression. |journal=Biochem. Soc. Trans. |volume=33 |issue= Pt 3 |pages= 471-3 |year= 2005 |pmid= 15916543 |doi= 10.1042/BST0330471 }}
*{{cite journal  | author=Rual JF, Venkatesan K, Hao T, ''et al.'' |title=Towards a proteome-scale map of the human protein-protein interaction network. |journal=Nature |volume=437 |issue= 7062 |pages= 1173-8 |year= 2005 |pmid= 16189514 |doi= 10.1038/nature04209 }}
*{{cite journal  | author=Borchers CH, Thapar R, Petrotchenko EV, ''et al.'' |title=Combined top-down and bottom-up proteomics identifies a phosphorylation site in stem-loop-binding proteins that contributes to high-affinity RNA binding. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=103 |issue= 9 |pages= 3094-9 |year= 2006 |pmid= 16492733 |doi= 10.1073/pnas.0511289103 }}
}}
{{refend}}
{{refend}}
{{protein-stub}}
{{WikiDoc Sources}}

Latest revision as of 12:00, 10 January 2019

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

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Ensembl

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UniProt

n/a

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RefSeq (mRNA)

n/a

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Histone RNA hairpin-binding protein or stem-loop binding protein (SLBP) is a protein that in humans is encoded by the SLBP gene.[1][2][3]

Species distribution

SLBP has been cloned from humans, C. elegans, D. melanogaster, X. laevis, and sea urchins. The full length human protein has 270 amino acids (31 kDa) with a centrally located RNA binding domain (RBD). The 75 amino acid RBD is well conserved across species, however the remainder of SLBP is highly divergent in most organisms and not homologous to any other protein in the eukaryotic genomes.

Function

This gene encodes a protein that binds to the histone 3' UTR stem-loop structure in replication-dependent histone mRNAs. Histone mRNAs do not contain introns or polyadenylation signals, and are processed by a single endonucleolytic cleavage event downstream of the stem-loop. The stem-loop structure is essential for efficient processing of the histone pre-mRNA but this structure also controls the transport, translation and stability of histone mRNAs. SLBP expression is regulated during S-phase of the cell cycle, increasing more than 10-fold during the latter part of G1.

All SLBP proteins are capable of forming a highly stable complex with histone stem-loop RNA. Complex formation with the histone mRNA stem-loop is achieved by a novel three-helix bundle fold. SLBP proteins also recognize the tetraloop structure of the histone hairpin, the base of the stem, and the 5' flanking region. The crystal structure of human SLBP in complex with the stem-loop RNA as well as the exonuclease Eri1 reveals that the Arg181 residue of SLBP specifically interacts with the second guanine base in the RNA stem.[4] The rest of the protein is intrinsically disordered in fruit-flies as well as in humans. A unique feature of the SLBP RBD is that it is phosphorylated in its RNA binding domain at the Thr171 residue. The SLBP RBD also undergoes proline isomerization about this sequence and is a substrate for the prolyl isomerase Pin1. The N-terminal domain of human SLBP is required for translation activation of histone mRNAs via its interaction with SLIP1. SLBP also interacts with the CBP80 associated protein CTIF to facilitate rapid degradation of histone mRNAs. SLBP is a phosphoprotein and besides T171, it is also phosphorylated at Ser7, Ser20, Ser23, Thr60, Thr61 in mammalian cells. The phosphorylation at Thr60 is mediated by CK2 and Thr61 is by Cyclin A/Cdk1.[3]

References

  1. ↑ Martin F, Schaller A, Eglite S, Schumperli D, Muller B (Mar 1997). "The gene for histone RNA hairpin binding protein is located on human chromosome 4 and encodes a novel type of RNA binding protein". EMBO J. 16 (4): 769–78. doi:10.1093/emboj/16.4.769. PMC 1169678. PMID 9049306.
  2. ↑ McCombie WR, Martin-Gallardo A, Gocayne JD, FitzGerald M, Dubnick M, Kelley JM, Castilla L, Liu LI, Wallace S, Trapp S (August 1992). "Expressed genes, Alu repeats and polymorphisms in cosmids sequenced from chromosome 4p16.3". Nature Genetics. 1 (5): 348–53. doi:10.1038/ng0892-348. PMID 1338771.
  3. ↑ 3.0 3.1 "Entrez Gene: SLBP stem-loop (histone) binding protein".
  4. ↑ Dazhi Tan; William F. Marzluff; Zbigniew Dominski; Liang Tong (Jan 2013). "Structure of Histone mRNA Stem-Loop, Human Stem-Loop Binding Protein, and 3′hExo Ternary Complex". Science. 339 (6117): 318–321. doi:10.1126/science.1228705. PMC 3552377. PMID 23329046.

Further reading

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