Zbtb33 Gene Knockout Changes Transcription of the Fgf9, Fgfr3, c-Myc and FoxG1 Genes in the Developing Mouse Brain

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Zbtb33 Gene Knockout Changes Transcription of the Fgf9, Fgfr3, c-Myc and FoxG1 Genes in the Developing Mouse Brain. / Illarionova, N. B.; Borisova, M. A.; Bazhenova, E. Y. et al.

In: Molecular Biology, Vol. 55, No. 3, 05.2021, p. 363-371.

Research output: Contribution to journal › Article › peer-review

Author

Illarionova, N. B. ; Borisova, M. A. ; Bazhenova, E. Y. et al. / Zbtb33 Gene Knockout Changes Transcription of the Fgf9, Fgfr3, c-Myc and FoxG1 Genes in the Developing Mouse Brain. In: Molecular Biology. 2021 ; Vol. 55, No. 3. pp. 363-371.

BibTeX

@article{60344fd21b854acbaebc107564cd7d62,

title = "Zbtb33 Gene Knockout Changes Transcription of the Fgf9, Fgfr3, c-Myc and FoxG1 Genes in the Developing Mouse Brain",

abstract = "The transcription factor KAISO is important for proper development of animal embryos. In the cell, KAISO regulates cell division and apoptosis. KAISO is abundant in the central nervous system. Here we describe the effects of Zbtb33 gene knockout on the transcription of several genes that regulate the development of the central nervous system, including Fgf9, Fgfr3, Sox9, Sox2, c-Myc, NeuroD1 and FoxG1. These genes are related to the Wnt/β-catenin signaling pathway, which is closely connected to KAISO. Hippocampal, frontal cortical, and striatal tissue from C57BL/6j mice with a knockout in the Zbtb33 gene encoding KAISO (ZBTB33-) and wild-type mice (ZBTB33 +) were collected and profiled at different stages of development. Age-dependent and region-specific differences in the mRNA levels of the Fgf9, Fgfr3, c-Myc, FoxG1 genes in the developing brain of ZBTB33– and ZBTB33+ mice were described and discussed.",

keywords = "Fgf9, Fgfr3, FoxG1, frontal cortex, hippocampus, Kaiso, mouse, Real-time PCR, striatum, Wnt/β-catenin signaling, с-Мyc",

author = "Illarionova, {N. B.} and Borisova, {M. A.} and Bazhenova, {E. Y.} and Zabelina, {D. S.} and Fursenko, {D. V.} and Kulikov, {A. V.}",

note = "Funding Information: The experimental part of the work was supported by a grant from the Russian Foundation for Basic Research (no. 18-04-00869 A, brain dissection, RNA isolation and real-time PCR) and budget project no. 0259-2021-0015 (housing and breeding animals) and was carried out using equipment belonging to the Shared Center for Genetic Resources of Laboratory Animals, Federal Research Center of ICG SB RAS, supported by the Ministry of Education and Science of Russia (Unique project identifier RFMEFI62119X0023). Publisher Copyright: {\textcopyright} 2021, Pleiades Publishing, Inc.",

year = "2021",

month = may,

doi = "10.1134/S0026893321020230",

language = "English",

volume = "55",

pages = "363--371",

journal = "Molecular Biology",

issn = "0026-8933",

publisher = "Maik Nauka-Interperiodica Publishing",

number = "3",

}

RIS

TY - JOUR

T1 - Zbtb33 Gene Knockout Changes Transcription of the Fgf9, Fgfr3, c-Myc and FoxG1 Genes in the Developing Mouse Brain

AU - Illarionova, N. B.

AU - Borisova, M. A.

AU - Bazhenova, E. Y.

AU - Zabelina, D. S.

AU - Fursenko, D. V.

AU - Kulikov, A. V.

N1 - Funding Information: The experimental part of the work was supported by a grant from the Russian Foundation for Basic Research (no. 18-04-00869 A, brain dissection, RNA isolation and real-time PCR) and budget project no. 0259-2021-0015 (housing and breeding animals) and was carried out using equipment belonging to the Shared Center for Genetic Resources of Laboratory Animals, Federal Research Center of ICG SB RAS, supported by the Ministry of Education and Science of Russia (Unique project identifier RFMEFI62119X0023). Publisher Copyright: © 2021, Pleiades Publishing, Inc.

PY - 2021/5

Y1 - 2021/5

N2 - The transcription factor KAISO is important for proper development of animal embryos. In the cell, KAISO regulates cell division and apoptosis. KAISO is abundant in the central nervous system. Here we describe the effects of Zbtb33 gene knockout on the transcription of several genes that regulate the development of the central nervous system, including Fgf9, Fgfr3, Sox9, Sox2, c-Myc, NeuroD1 and FoxG1. These genes are related to the Wnt/β-catenin signaling pathway, which is closely connected to KAISO. Hippocampal, frontal cortical, and striatal tissue from C57BL/6j mice with a knockout in the Zbtb33 gene encoding KAISO (ZBTB33-) and wild-type mice (ZBTB33 +) were collected and profiled at different stages of development. Age-dependent and region-specific differences in the mRNA levels of the Fgf9, Fgfr3, c-Myc, FoxG1 genes in the developing brain of ZBTB33– and ZBTB33+ mice were described and discussed.

AB - The transcription factor KAISO is important for proper development of animal embryos. In the cell, KAISO regulates cell division and apoptosis. KAISO is abundant in the central nervous system. Here we describe the effects of Zbtb33 gene knockout on the transcription of several genes that regulate the development of the central nervous system, including Fgf9, Fgfr3, Sox9, Sox2, c-Myc, NeuroD1 and FoxG1. These genes are related to the Wnt/β-catenin signaling pathway, which is closely connected to KAISO. Hippocampal, frontal cortical, and striatal tissue from C57BL/6j mice with a knockout in the Zbtb33 gene encoding KAISO (ZBTB33-) and wild-type mice (ZBTB33 +) were collected and profiled at different stages of development. Age-dependent and region-specific differences in the mRNA levels of the Fgf9, Fgfr3, c-Myc, FoxG1 genes in the developing brain of ZBTB33– and ZBTB33+ mice were described and discussed.

KW - Fgf9

KW - Fgfr3

KW - FoxG1

KW - frontal cortex

KW - hippocampus

KW - Kaiso

KW - mouse

KW - Real-time PCR

KW - striatum

KW - Wnt/β-catenin signaling

KW - с-Мyc

UR - http://www.scopus.com/inward/record.url?scp=85121437061&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/7725ac08-df15-3fcd-9b90-7dc29ab0563a/

U2 - 10.1134/S0026893321020230

DO - 10.1134/S0026893321020230

M3 - Article

AN - SCOPUS:85121437061

VL - 55

SP - 363

EP - 371

JO - Molecular Biology

JF - Molecular Biology

SN - 0026-8933

IS - 3

ER -

ID: 35041471