Cited by 156Developmental Biology and Gene RegulationNeurogenesis and neuroplasticity mechanismsGenomics and Chromatin Dynamics

CTIP1 and CTIP2 are differentially expressed during mouse embryogenesis

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Leid, Mark, Ishmael, Jane E., Avram, Dorina, Shepherd, David, Fraulob, Valérie, Dollé, Pascal·2004·Gene Expression Patterns

Abstract

Chicken ovalbumin upstream promoter transcription factor-interacting proteins 1 and 2 (CTIP1 and CTIP2) are related transcriptional regulatory proteins. While overexpression of both of these proteins has been linked to the development of several lymphoid malignancies, lack of CTIP1 and CTIP2 expression results in defective lymphopoiesis and abnormal thymocyte development, respectively. Here, we describe the expression patterns of CTIP1 and CTIP2 during mouse embryogenesis and in the post-natal brain. Both CTIP1 and CTIP2 were expressed diffusely in the embryo at 10.5 days post-coitum (d.p.c.). However, the expression of both genes became increasingly restricted to the central nervous system (CNS) during the course of fetal development, culminating with high, but differential, expression levels throughout the hippocampal subregions, olfactory bulb and cortex, limbic system, basal ganglia and frontal cortex of the developing brain, and in dorsal cells of the spinal cord. The brain expression domains of CTIP1 and CTIP2 were maintained into adulthood. Outside the CNS, both genes exhibited differential expression within the facial mesenchyme at 12.5 d.p.c., and CTIP2 was selectively expressed from day 12.5 onwards in the olfactory epithelium and developing thymus, and to a lesser extent in oral and gut epithelia. Strong CTIP2 expression was maintained in the thymus at 18.5 d.p.c. These results support the selective contributions of both CTIP1 and CTIP2 in the development and function of both the central nervous and immune systems and the importance of future investigations to define the function(s) of both proteins.

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Crossref · 10.1016/j.modgep.2004.03.009

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  1. Avram D, Fields A, Pretty On Top K, Nevrivy DJ, Ishmael JE, Leid M. Isolation of a novel family of C(2)H(2) zinc finger proteins implicated in transcriptional repression mediated by chicken ovalbumin upstream promoter transcription factor (COUP-TF) orphan nuclear receptors. J. Biol. Chem. 2000;275:10315–10322. doi: 10.1074/jbc.275.14.10315. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  2. Avram D, Fields A, Senawong T, Topark-Ngarm A, Leid M. COUP-TF (chicken ovalbumin upstream promoter transcription factor)-interacting protein 1 (CTIP1) is a sequence-specific DNA binding protein. Biochem. J. 2002;368:555–563. doi: 10.1042/BJ20020496. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  3. Ghez C, Thack WT. The cerebellum. In: Kandel ER, et al., editors. Principles of Neural Science. New York: McGraw-Hill; 2000. pp. 832–852. [Google Scholar]
  4. Gunnersen JM, Augustine C, Spirkoska V, Kim M, Brown M, Tan SS. Global analysis of gene expression patterns in developing mouse neocortex using serial analysis of gene expression. Mol. Cell. Neurosci. 2002;19:560–573. doi: 10.1006/mcne.2001.1098. [DOI] [PubMed] [Google Scholar] · DOI
  5. Jonk LJ, de Jonge ME, Pals CE, Wissink S, Vervaart JM, Schoorlemmer J, Kruijer W. Cloning and expression during development of three murine members of the COUP family of nuclear orphan receptors. Mech. Dev. 1994;47:81–97. doi: 10.1016/0925-4773(94)90098-1. [DOI] [PubMed] [Google Scholar] · DOI
  6. Liu Q, Dwyer ND, O’Leary DD. Differential expression of COUP-TFI, CHL1, and two novel genes in developing neocortex identified by differential display PCR. J. Neurosci. 2000;20:7682–7690. doi: 10.1523/JNEUROSCI.20-20-07682.2000. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  7. Lopes da Silva S, Cox JJ, Jonk LJ, Kruijer W, Burbach JP. Localization of transcripts of the related nuclear orphan receptors COUP-TF I and ARP-1 in the adult mouse brain. Brain Res. Mol. Brain Res. 1995;30:131–136. doi: 10.1016/0169-328x(94)00289-q. [DOI] [PubMed] [Google Scholar] · DOI
  8. Nakamura T, Yamazaki Y, Saiki Y, Moriyama M, Largaespada DA, Jenkins NA, Copeland NG. Evi9 encodes a novel zinc finger protein that physically interacts with BCL6, a known human B-cell proto-oncogene product. Mol. Cell. Biol. 2000;20:3178–3186. doi: 10.1128/mcb.20.9.3178-3186.2000. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  9. Niederreither K, Dolle P. In situ hybridization with 35S-labeled probes for retinoid receptors. Methods Mol. Biol. 1998;89:247–267. doi: 10.1385/0-89603-438-0:247. [DOI] [PubMed] [Google Scholar] · DOI
  10. Qiu Y, Cooney AJ, Kuratani S, DeMayo FJ, Tsai SY, Tsai MJ. Spatiotemporal expression patterns of chicken ovalbumin upstream promoter-transcription factors in the developing mouse central nervous system: evidence for a role in segmental patterning of the diencephalon. Proc. Natl Acad. Sci. USA. 1994;91:4451–4455. doi: 10.1073/pnas.91.10.4451. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  11. Rohr O, Lecestre D, Chasserot-Golaz S, Marban C, Avram D, Aunis D, et al. Recruitment of Tat to heterochromatin protein HP1 via interaction with CTIP2 inhibits human immunodeficiency virus type 1 replication in microglial cells. J. Virol. 2003;77:5415–5427. doi: 10.1128/JVI.77.9.5415-5427.2003. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  12. Saiki Y, Yamazaki Y, Yoshida M, Katoh O, Nakamura T. Human EVI9, a homologue of the mouse myeloid leukemia gene, is expressed in the hematopoietic progenitors and down-regulated during myeloid differentiation of HL60 cells. Genomics. 2000;70:387–391. doi: 10.1006/geno.2000.6385. [DOI] [PubMed] [Google Scholar] · DOI
  13. Satterwhite E, Sonoki T, Willis TG, Harder L, Nowak R, Arriola EL, et al. The BCL11 gene family: involvement of BCL11A in lymphoid malignancies. Blood. 2001;98:3413–3420. doi: 10.1182/blood.v98.12.3413. [DOI] [PubMed] [Google Scholar] · DOI
  14. Senawong T, Peterson VJ, Avram D, Shepherd DM, Frye RA, Minucci S, Leid M. Involvement of the histone deacetylase SIRT1 in COUP-TF-interacting protein 2-mediated transcriptional repression. J. Biol. Chem. 2003;278:43041–43050. doi: 10.1074/jbc.M307477200. [DOI] [PMC free article] [PubMed] [Google Scholar] · DOI
  15. Wakabayashi Y, Inoue J, Takahashi Y, Matsuki A, Kosugi-Okano H, Shinbo T, et al. Homozygous deletions and point mutations of the Rit1/Bcl11b gene in gamma-ray induced mouse thymic lymphomas. Biochem. Biophys. Res. Commun. 2003a;301:598–603. doi: 10.1016/s0006-291x(02)03069-3. [DOI] [PubMed] [Google Scholar] · DOI
  16. Wakabayashi Y, Watanabe H, Inoue J, Takeda N, Sakata J, Mishima Y, et al. Bcl11b is required for differentiation and survival of alphabeta T lymphocytes. Nat. Immunol. 2003b;4:533–539. doi: 10.1038/ni927. [DOI] [PubMed] [Google Scholar] · DOI
  17. Zhou C, Qiu Y, Pereira FA, Crair MC, Tsai SY, Tsai MJ. The nuclear orphan receptor COUP-TFI is required for differentiation of subplate neurons and guidance of thalamocortical axons. Neuron. 1999;24:847–859. doi: 10.1016/s0896-6273(00)81032-6. [DOI] [PubMed] [Google Scholar] · DOI

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Authors
Leid, M., Ishmael, J. E., Avram, D., Shepherd, D., Fraulob, V., & Dollé, P.
Affiliations
  • Oregon State University (US)
  • Albany Medical College (US)
  • University of Montana (US)
  • Centre National de la Recherche Scientifique (FR)
Corresponding author
Leid, Mark
Venue
Gene Expression Patterns
Publisher
Elsevier BV
Published
2004-10
Volume
4
Issue
6
Pages
733-739
ISSN
1567-133X (ISSN-L)
OpenAlex
W2088654564
Cited by
156
References
1
Citations by year
2026: 3 · 2025: 4 · 2024: 11 · 2023: 14 · 2022: 5 · 2021: 8 · 2020: 7 · 2019: 7 · 2018: 8 · 2017: 9 · 2016: 8 · 2015: 6 · 2014: 6 · 2013: 5 · 2012: 13
FWCI
1.19
Type
journal article
Language
en
Open access
Locations
  • Gene Expression Patterns (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
  • HAL (submittedVersion)
Funders
  • Oregon State University
  • National Institutes of Health
  • National Institute of General Medical Sciences (GM 60852, R01GM060852)
  • National Institute of Environmental Health Sciences (ES-00-210, P30ES000210)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
Keywords
CTIP2, mouse embryo development, central nervous system development, brain development, thymus development, olfactory epithelium, facial mesenchyme, hippocampus, olfactory bulb, T cell development, lymphocyte development, transcriptional regulatory proteins
MeSH terms
Animals, Brain, Carrier Proteins, Central Nervous System, Cerebellum, DNA-Binding Proteins, Hippocampus, Immune System, Models, Biological, Nuclear Proteins, Receptors, Steroid, Repressor Proteins, Time Factors, Transcription Factors, In Situ Hybridization, Gene Expression Regulation, Developmental, Mice, COUP Transcription Factors

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