XPB — разлика између измена

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м додана категорија Поправка ДНК помоћу геџета HotCat
 
(Није приказано 13 међуизмена 9 корисника)
Ред 1:
{{PBB|geneid=2071}}
-{'''XPB'''}- (-{Xeroderma Pigmentosum B}-) je [[Adenozin trifosfat|ATP]] zavisna ljudska DNK [[helikaza]] koja je deo kompleksa [[Transkripcioni faktor II H|TFIIH]] [[Transkripcioni faktor|transkripcionog faktora]]. 3D struktura -{XPB}- homologa je kristalografski.<ref>{{cite journal |authorvauthors=Fan L, Arvai A, Cooper P, Iwai S, Hanaoka F, Tainer J |title=Conserved XPB core structure and motifs for DNA unwinding: implications for pathway selection of transcription or excision repair |journal=Mol Cell |volume=22 |issue=1 |pages=27–37 |year=2006 |pmid=16600867 |doi=10.1016/j.molcel.2006.02.017|pages=27–37}}</ref>
 
== Funkcija ==
-{XPB}- učestvuje u normalnoj bazalnoj transkripciji, [[Transkripciono spregnuta popravka|transkripciono spregnutoj popravci]] (TCR), i [[Popravka isecanjem nukleotida|popravci isecanjem nukleotida]] (-{NER}-). Pokazano jed a prečišćeni -{XPB}- razvija DNK u 3’-5’ pravcu.
 
== Interakcije ==
-{XPB}- formira [[Protein-protein interakcija|interakcije]] sa [[XPC (gen)|-{XPC}-]],<ref name="pmid10734143">{{cite journal |last=Yokoi |first=M |authorlinkdisplay-authors= |coauthors=Masutani C, Maekawa T, Sugasawa K, Ohkuma Y, Hanaoka Fetal |year=2000|month=March |title=The xeroderma pigmentosum group C protein complex XPC-HR23B plays an important role in the recruitment of transcription factor IIH to damaged DNA |journal=J. Biol. Chem. |volume=275 |issue=13 |pages=9870–5 |publisher= |location = UNITED STATES| issn = 0021-9258| pmid = 10734143 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |doi=10.1074/jbc.275.13.9870 |pages=9870–5}}</ref> [[BCR gen|-{BCR}- genom]],<ref name="pmid9874796">{{cite journal |last=Takeda |first=N |authorlinkdisplay-authors= |coauthors=Shibuya M, Maru Yetal |year=1999|month=January |title=The BCR-ABL oncoprotein potentially interacts with the xeroderma pigmentosum group B protein |journal= Proc. Natl. Acad. Sci. U.S.A. |volume=96 |issue=1 |pages=203–7 |publisher= |location = UNITED STATES| issn = 0027-8424| pmid = 9874796 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |doi=10.1073/pnas.96.1.203 |pmc=15117 |pages=203–7}}</ref> -{[[ERCC2]]}-,<ref name="pmid15220921">{{cite journal |last=Giglia-Mari |first=Giuseppina |authorlinkdisplay-authors= |coauthors=Coin Frederic, Ranish Jeffrey A, Hoogstraten Deborah, Theil Arjan, Wijgers Nils, Jaspers Nicolaas G J, Raams Anja, Argentini Manuela, van der Spek P J, Botta Elena, Stefanini Miria, Egly Jean-Marc, Aebersold Ruedi, Hoeijmakers Jan H J, Vermeulen Wimetal |year=2004|month=July |title=A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A |journal=Nat. Genet. |volume=36 |issue=7 |pages=714–9 |publisher= |location = United States| issn = 1061-4036| pmid = 15220921 |doi = 10.1038/ng1387 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |unused_data=DUPLICATE DATA: pmid = 15226750 }}</ref><ref name="pmid9118947">{{cite journal |last=Marinoni |first=J C |authorlinkdisplay-authors= |coauthors=Roy R, Vermeulen W, Miniou P, Lutz Y, Weeda G, Seroz T, Gomez D M, Hoeijmakers J H, Egly J M etal|year=1997|month=March |title=Cloning and characterization of p52, the fifth subunit of the core of the transcription/DNA repair factor TFIIH |journal=EMBO J. |volume=16 |issue=5 |pages=1093–102 |publisher= |location = ENGLAND| issn = 0261-4189| pmid = 9118947 |doi = 10.1093/emboj/16.5.1093 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |pmc=1169708 |pages=714–9}}</ref><ref name="pmid8152490">{{cite journal |last=Drapkin |first=R |authorlinkdisplay-authors= |coauthors=Reardon J T, Ansari A, Huang J C, Zawel L, Ahn K, Sancar A, Reinberg Detal |year=1994|month=April |title=Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II |journal= Nature |volume=368 |issue=6473 |pages=769–72 |publisher= |location = ENGLAND| issn = 0028-0836| pmid = 8152490 |doi = 10.1038/368769a0 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |pages=769–72}}</ref><ref name="pmid8652557">{{cite journal |last=Iyer |first=N |authorlinkdisplay-authors= |coauthors=Reagan M S, Wu K J, Canagarajah B, Friedberg E Cetal |year=1996|month=February |title=Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein |journal=Biochemistry |volume=35 |issue=7 |pages=2157–67 |publisher= |location = UNITED STATES| issn = 0006-2960| pmid = 8652557 |doi = 10.1021/bi9524124 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |pages=2157–67}}</ref> -{[[P53]]}-,<ref name="pmid7663514">{{cite journal |last=Wang |first=X W |authorlinkdisplay-authors= |coauthors=Yeh H, Schaeffer L, Roy R, Moncollin V, Egly J M, Wang Z, Freidberg E C, Evans M K, Taffe B G etal|year=1995|month=June |title=p53 modulation of TFIIH-associated nucleotide excision repair activity |journal=Nat. Genet. |volume=10 |issue=2 |pages=188–95 |publisher= |location = UNITED STATES| issn = 1061-4036| pmid = 7663514 |doi = 10.1038/ng0695-188 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |pages=188–95}}</ref> -{[[GTF2H2]]}-,<ref name="pmid15220921"/><ref name="pmid9118947"/> -{[[GTF2H1]]}-,<ref name="pmid15220921"/><ref name="pmid9118947"/><ref name="pmid9130708">{{cite journal |last=Rossignol |first=M |authorlinkdisplay-authors= |coauthors=Kolb-Cheynel I, Egly J Metal |year=1997|month=April |title=Substrate specificity of the cdk-activating kinase (CAK) is altered upon association with TFIIH |journal=EMBO J. |volume=16 |issue=7 |pages=1628–37 |publisher= |location = ENGLAND| issn = 0261-4189| pmid = 9130708 |doi = 10.1093/emboj/16.7.1628 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |pmc=1169767 |pages=1628–37}}</ref> -{[[GTF2H5]]}-,<ref name="pmid15220921"/> [[Ciklin zavisna kinaza 7|ciklin zavisnom kinazom]],<ref name="pmid15220921"/><ref name="pmid9130708"/><ref name="pmid8521393">{{cite journal |last=Yee |first=A |authorlinkdisplay-authors= |coauthors=Nichols M A, Wu L, Hall F L, Kobayashi R, Xiong Yetal |year=1995|month=December |title=Molecular cloning of CDK7-associated human MAT1, a cyclin-dependent kinase-activating kinase (CAK) assembly factor |journal=Cancer Res. |volume=55 |issue=24 |pages=6058–62 |publisher= |location = UNITED STATES| issn = 0008-5472| pmid = 8521393 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |pages=6058–62}}</ref> -{[[PSMC5]]}-<ref name="pmid9173976">{{cite journal |last=Weeda |first=G |authorlinkdisplay-authors= |coauthors=Rossignol M, Fraser R A, Winkler G S, Vermeulen W, van 't Veer L J, Ma L, Hoeijmakers J H, Egly J Metal |year=1997|month=June |title=The XPB subunit of repair/transcription factor TFIIH directly interacts with SUG1, a subunit of the 26S proteasome and putative transcription factor |journal=Nucleic Acids Res. |volume=25 |issue=12 |pages=2274–83 |publisher= |location = ENGLAND| issn = 0305-1048| pmid = 9173976 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |doi=10.1093/nar/25.12.2274 |pmc=146752 |pages=2274–83}}</ref> i -{[[GTF2H4]]}-.<ref name="pmid15220921"/><ref name="pmid9118947"/>
 
== Literatura ==
{{refbeginЛитература | 2}}
{{PBB_Further_reading
| citations =
* {{cite journal | authorlast=Jeang KT |first=Jeang|title=Tat, Tat-associated kinase, and transcription. |journal=J. Biomed. Sci. |volume=5 |issue= 1 |pages= 24–7 |year= 1998 |pmid= 9570510 |doi=10.1007/BF02253352 |pages=24–7}}
* {{cite journal | authorvauthors=Yankulov K, Bentley D |title=Transcriptional control: Tat cofactors and transcriptional elongation. |journal=Curr. Biol. |volume=8 |issue= 13 |pages= R447–9 |year= 1998 |pmid= 9651670 |doi=10.1016/S0960-9822(98)70289-1 }}
* {{cite journal | authorvauthors=Cleaver JE, Thompson LH, Richardson AS, States JC |title=A summary of mutations in the UV-sensitive disorders: xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy. |journal=Hum. Mutat. |volume=14 |issue= 1 |pages= 9–22 |year= 1999 |pmid= 10447254 |doi= 10.1002/(SICI)1098-1004(1999)14:1<9::AID-HUMU2>3.0.CO;2-6 |pages=9–22}}
* {{cite journal | authorlast1=Ma L, |first1=Ma|author2=Weeda G, Jochemsen |last3=AG, ''et al.'' |first3=Jochemsen|display-authors=etal|title=Molecular and functional analysis of the XPBC/ERCC-3 promoter: transcription activity is dependent on the integrity of an Sp1-binding site. |journal=Nucleic Acids Res. |volume=20 |issue= 2 |pages= 217–24 |year= 1992 |pmid= 1741247 |doi=10.1093/nar/20.2.217 | pmc=310357 |pages=217–24}}
* {{cite journal | authorlast1=G|first1=Weeda G, |author2=Wiegant J, |author3=van der Ploeg M, ''et al.'' |display-authors=etal|title=Localization of the xeroderma pigmentosum group B-correcting gene ERCC3 to human chromosome 2q21. |journal=Genomics |volume=10 |issue= 4 |pages= 1035–1040 |year= 1991 |pmid= 1916809 |doi=10.1016/0888-7543(91)90195-K |pages=1035–1040}}
* {{cite journal | authorlast1=Weeda G, |first1=Weeda|author2=Ma LB, |author3=van Ham RC, ''et al.'' |display-authors=etal|title=Structure and expression of the human XPBC/ERCC-3 gene involved in DNA repair disorders xeroderma pigmentosum and Cockayne's syndrome. |journal=Nucleic Acids Res. |volume=19 |issue= 22 |pages= 6301–6308 |year= 1991 |pmid= 1956789 |doi=10.1093/nar/19.22.6301 | pmc=329143 |pages=6301–6308}}
* {{cite journal | authorlast1=Weeda G, |first1=Weeda|author2=van Ham RC, Masurel |last3=R, ''et al.'' |first3=Masurel|display-authors=etal|title=Molecular cloning and biological characterization of the human excision repair gene ERCC-3. |url=https://archive.org/details/sim_molecular-and-cellular-biology_1990-06_10_6/page/2570|journal=Mol. Cell. Biol. |volume=10 |issue= 6 |pages= 2570–2581 |year= 1990 |pmid= 2111438 |doi= | pmc=360615 |pages=2570–2581}}
* {{cite journal | authorlast1=Weeda G, |first1=Weeda|author2=van Ham RC, |last3=W|first3=Vermeulen W, ''et al.'' |display-authors=etal|title=A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome. |journal=Cell |volume=62 |issue= 4 |pages= 777–91 |year= 1990 |pmid= 2167179 |doi=10.1016/0092-8674(90)90122-U |pages=777–91}}
* {{cite journal | authorlast1=XW|first1=Wang XW, |author2=Yeh H, Schaeffer |last3=L, ''et al.'' |first3=Schaeffer|display-authors=etal|title=p53 modulation of TFIIH-associated nucleotide excision repair activity. |journal=Nat. Genet. |volume=10 |issue= 2 |pages= 188–95 |year= 1995 |pmid= 7663514 |doi= 10.1038/ng0695-188 |pages=188–95}}
* {{cite journal | authorvauthors=Maxon ME, Goodrich JA, Tjian R |title=Transcription factor IIE binds preferentially to RNA polymerase IIa and recruits TFIIH: a model for promoter clearance. |journal=Genes Dev. |volume=8 |issue= 5 |pages= 515–24 |year= 1994 |pmid= 7926747 |doi=10.1101/gad.8.5.515 |pages=515–24}}
* {{cite journal | authorvauthors=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1–2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=10.1016/0378-1119(94)90802-8 |pages=171–4}}
* {{cite journal | authorlast1=R|first1=Drapkin R, |author2=Reardon JT, Ansari |last3=A, ''et al.'' |first3=Ansari|display-authors=etal|title=Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II |journal=Nature |volume=368 |issue= 6473 |pages= 769–72 |year= 1994 |pmid= 8152490 |doi= 10.1038/368769a0 |pages=769–72}}
* {{cite journal | authorauthor1=van Vuuren AJ, Vermeulen |last2=W, |first2=Vermeulen|author3=Ma L, ''et al.'' |display-authors=etal|title=Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH) |journal=EMBO J. |volume=13 |issue= 7 |pages= 1645–1653 |year= 1994 |pmid= 8157004 |doi= | pmc=394995 |pages=1645–1653}}
* {{cite journal | authorlast1=L|first1=Schaeffer L, |author2=Moncollin V, |last3=R|first3=Roy R, ''et al.'' |display-authors=etal|title=The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor |journal=EMBO J. |volume=13 |issue= 10 |pages= 2388–2392 |year= 1994 |pmid= 8194528 |doi= | pmc=395103 |pages=2388–2392}}
* {{cite journal | authorlast1=SN|first1=Guzder SN, |author2=Sung P, Bailly |last3=V, ''et al.'' |first3=Bailly|display-authors=etal|title=RAD25 is a DNA helicase required for DNA repair and RNA polymerase II transcription |journal=Nature |volume=369 |issue= 6481 |pages= 578–81 |year= 1994 |pmid= 8202161 |doi= 10.1038/369578a0 |pages=578–81}}
* {{cite journal | authorlast1=Vermeulen W, |first1=Vermeulen|author2=Scott RJ, Rodgers |last3=S, ''et al.'' |first3=Rodgers|display-authors=etal|title=Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3 |url=https://archive.org/details/sim_american-journal-of-human-genetics_1994-02_54_2/page/191|journal=Am. J. Hum. Genet. |volume=54 |issue= 2 |pages= 191–200 |year= 1994 |pmid= 8304337 |doi= | pmc=1918172 |pages=191–200}}
* {{cite journal | authorlast1=Scott RJ, |first1=Scott|author2=Itin P, Kleijer |last3=WJ, ''et al.'' |first3=Kleijer|display-authors=etal|title=Xeroderma pigmentosum-Cockayne syndrome complex in two patients: absence of skin tumors despite severe deficiency of DNA excision repair |journal=J. Am. Acad. Dermatol. |volume=29 |issue= 5 Pt 2 |pages= 883–9 |year= 1993 |pmid= 8408834 |doi=10.1016/0190-9622(93)70263-S |pages=883–9}}
* {{cite journal | authorlast1=Blau J, |first1=Blau|author2=Xiao H, McCracken |last3=S, ''et al.'' |first3=McCracken|display-authors=etal|title=Three functional classes of transcriptional activation domain |url=https://archive.org/details/sim_molecular-and-cellular-biology_1996-05_16_5/page/2044|journal=Mol. Cell. Biol. |volume=16 |issue= 5 |pages= 2044–2055 |year= 1996 |pmid= 8628270 |doi= | pmc=231191 |pages=2044–2055}}
* {{cite journal | authorlast1=Iyer N, |first1=Iyer|author2=Reagan MS, |last3=KJ|first3=Wu KJ, ''et al.'' |display-authors=etal|title=Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein |journal=Biochemistry |volume=35 |issue= 7 |pages= 2157–2167 |year= 1996 |pmid= 8652557 |doi= 10.1021/bi9524124 |pages=2157–2167}}
* {{cite journal | authorlast1=Hwang JR, |first1=Hwang|author2=Moncollin V, |last3=W|first3=Vermeulen W, ''et al.'' |display-authors=etal|title=A 3' --> 5' XPB helicase defect in repair/transcription factor TFIIH of xeroderma pigmentosum group B affects both DNA repair and transcription |journal=J. Biol. Chem. |volume=271 |issue= 27 |pages= 15898–904 |year= 1996 |pmid= 8663148 |doi=10.1074/jbc.271.27.15898 |pages=15898–904}}
}}
{{Литература крај}}
{{refend}}
 
== Reference ==
Ред 41:
* [[Kseroderma pigmentozum]]
 
== Spoljašnje veze ==
* [http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=xp -{Xeroderma Pigmentosum}-]
* {{MeshName|XPBC-ERCC-3+protein}}
 
{{normativna kontrola}}
 
[[Категорија:Поправка ДНК]]
 
[[de:TFIIH-Helikase XPB]]
[[en:XPB]]