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AP1-подобные цис-элементы в 5'-регуляторной области гена аполипопротеина A-I человека. / Lapikov, I. A.; Mogilenko, D. A.; Dizhe, E. B.; Ignatovich, I. A.; Orlov, S. V.; Perevozchikov, A. P.

In: МОЛЕКУЛЯРНАЯ БИОЛОГИЯ, Vol. 42, No. 2, 03.2008, p. 295-305.

Research output: Contribution to journalArticlepeer-review

Harvard

Lapikov, IA, Mogilenko, DA, Dizhe, EB, Ignatovich, IA, Orlov, SV & Perevozchikov, AP 2008, 'AP1-подобные цис-элементы в 5'-регуляторной области гена аполипопротеина A-I человека', МОЛЕКУЛЯРНАЯ БИОЛОГИЯ, vol. 42, no. 2, pp. 295-305.

APA

Lapikov, I. A., Mogilenko, D. A., Dizhe, E. B., Ignatovich, I. A., Orlov, S. V., & Perevozchikov, A. P. (2008). AP1-подобные цис-элементы в 5'-регуляторной области гена аполипопротеина A-I человека. МОЛЕКУЛЯРНАЯ БИОЛОГИЯ, 42(2), 295-305.

Vancouver

Lapikov IA, Mogilenko DA, Dizhe EB, Ignatovich IA, Orlov SV, Perevozchikov AP. AP1-подобные цис-элементы в 5'-регуляторной области гена аполипопротеина A-I человека. МОЛЕКУЛЯРНАЯ БИОЛОГИЯ. 2008 Mar;42(2):295-305.

Author

Lapikov, I. A. ; Mogilenko, D. A. ; Dizhe, E. B. ; Ignatovich, I. A. ; Orlov, S. V. ; Perevozchikov, A. P. / AP1-подобные цис-элементы в 5'-регуляторной области гена аполипопротеина A-I человека. In: МОЛЕКУЛЯРНАЯ БИОЛОГИЯ. 2008 ; Vol. 42, No. 2. pp. 295-305.

BibTeX

@article{5089cffb555d443ba8c699e439dcf066,
title = "AP1-подобные цис-элементы в 5'-регуляторной области гена аполипопротеина A-I человека",
abstract = "Several Ap1-like cis-acting elements were found within 5'-regulatory region (-2497...+173 versus transcription start point) of human apolipoprotein A-I gene (5'-apoA-I). Those elements are capable to interact with transcription factors belonging to Ap1 and CREB/ATF families. Those elements are localized outside of the hepatic enhancer (-220...-110) and the sequence responsible for apoA-I gene transcription in Caco2 cells (-595...-192). One of Ap1-like sites (5'-TGAGGTCT-3, Cre/jun2/apo) is present within 5'-apoA-I in two copies - distal (-1798 ...-1791) and proximal (+99...+106) ones. This and other Ap1-like sites - 5'-TGACTCT-3' (-1798...-1791, PF1) and 5'-TGACATCA-3' (-1171...-1163, Cre/jun1) were characterized by EMSA. It was shown by using the specific antibodies to c-Jun and ATF2 transcription factors in EMSA supershift experiments, that the DNA-protein complexes formed by Cre/jun2/apo, Cre/jun1 elements with nuclear proteins of human hepatoma HepG2 cells contain ATF2. The functional role of 5'-apoA-I regions containing Ap1-like sites was studied in cotransfection experiments of HepG2 cells (synthesize endogenous ApoA-I), human duodenum adenocarcinoma Hutu80 cells (do not synthesize endogenous ApoA-I), human neuroblastoma SK-N-SH cells (do not synthesize endogenous A-I) with expression vectors of c-jun and mekk1 genes. It was shown, that those Ap1-like sites appears to be responsible (the proximal Cre/jun2/apo is more efficient) for tissue-specific regulation of human apoA-I gene expression.",
author = "Lapikov, {I. A.} and Mogilenko, {D. A.} and Dizhe, {E. B.} and Ignatovich, {I. A.} and Orlov, {S. V.} and Perevozchikov, {A. P.}",
year = "2008",
month = mar,
language = "русский",
volume = "42",
pages = "295--305",
journal = "МОЛЕКУЛЯРНАЯ БИОЛОГИЯ",
issn = "0026-8984",
publisher = "Российская академия наук",
number = "2",

}

RIS

TY - JOUR

T1 - AP1-подобные цис-элементы в 5'-регуляторной области гена аполипопротеина A-I человека

AU - Lapikov, I. A.

AU - Mogilenko, D. A.

AU - Dizhe, E. B.

AU - Ignatovich, I. A.

AU - Orlov, S. V.

AU - Perevozchikov, A. P.

PY - 2008/3

Y1 - 2008/3

N2 - Several Ap1-like cis-acting elements were found within 5'-regulatory region (-2497...+173 versus transcription start point) of human apolipoprotein A-I gene (5'-apoA-I). Those elements are capable to interact with transcription factors belonging to Ap1 and CREB/ATF families. Those elements are localized outside of the hepatic enhancer (-220...-110) and the sequence responsible for apoA-I gene transcription in Caco2 cells (-595...-192). One of Ap1-like sites (5'-TGAGGTCT-3, Cre/jun2/apo) is present within 5'-apoA-I in two copies - distal (-1798 ...-1791) and proximal (+99...+106) ones. This and other Ap1-like sites - 5'-TGACTCT-3' (-1798...-1791, PF1) and 5'-TGACATCA-3' (-1171...-1163, Cre/jun1) were characterized by EMSA. It was shown by using the specific antibodies to c-Jun and ATF2 transcription factors in EMSA supershift experiments, that the DNA-protein complexes formed by Cre/jun2/apo, Cre/jun1 elements with nuclear proteins of human hepatoma HepG2 cells contain ATF2. The functional role of 5'-apoA-I regions containing Ap1-like sites was studied in cotransfection experiments of HepG2 cells (synthesize endogenous ApoA-I), human duodenum adenocarcinoma Hutu80 cells (do not synthesize endogenous ApoA-I), human neuroblastoma SK-N-SH cells (do not synthesize endogenous A-I) with expression vectors of c-jun and mekk1 genes. It was shown, that those Ap1-like sites appears to be responsible (the proximal Cre/jun2/apo is more efficient) for tissue-specific regulation of human apoA-I gene expression.

AB - Several Ap1-like cis-acting elements were found within 5'-regulatory region (-2497...+173 versus transcription start point) of human apolipoprotein A-I gene (5'-apoA-I). Those elements are capable to interact with transcription factors belonging to Ap1 and CREB/ATF families. Those elements are localized outside of the hepatic enhancer (-220...-110) and the sequence responsible for apoA-I gene transcription in Caco2 cells (-595...-192). One of Ap1-like sites (5'-TGAGGTCT-3, Cre/jun2/apo) is present within 5'-apoA-I in two copies - distal (-1798 ...-1791) and proximal (+99...+106) ones. This and other Ap1-like sites - 5'-TGACTCT-3' (-1798...-1791, PF1) and 5'-TGACATCA-3' (-1171...-1163, Cre/jun1) were characterized by EMSA. It was shown by using the specific antibodies to c-Jun and ATF2 transcription factors in EMSA supershift experiments, that the DNA-protein complexes formed by Cre/jun2/apo, Cre/jun1 elements with nuclear proteins of human hepatoma HepG2 cells contain ATF2. The functional role of 5'-apoA-I regions containing Ap1-like sites was studied in cotransfection experiments of HepG2 cells (synthesize endogenous ApoA-I), human duodenum adenocarcinoma Hutu80 cells (do not synthesize endogenous ApoA-I), human neuroblastoma SK-N-SH cells (do not synthesize endogenous A-I) with expression vectors of c-jun and mekk1 genes. It was shown, that those Ap1-like sites appears to be responsible (the proximal Cre/jun2/apo is more efficient) for tissue-specific regulation of human apoA-I gene expression.

UR - http://www.scopus.com/inward/record.url?scp=48049097054&partnerID=8YFLogxK

M3 - статья

C2 - 18610838

AN - SCOPUS:48049097054

VL - 42

SP - 295

EP - 305

JO - МОЛЕКУЛЯРНАЯ БИОЛОГИЯ

JF - МОЛЕКУЛЯРНАЯ БИОЛОГИЯ

SN - 0026-8984

IS - 2

ER -

ID: 91966248