Type |
Details |
Score |
Allele |
Name: |
nuclear factor I/X; endonuclease-mediated mutation 2, Harwell |
Allele Type: |
Endonuclease-mediated |
Attribute String: |
Modified isoform(s) |
|
•
•
•
•
•
|
Publication |
First Author: |
Qin K |
Year: |
2022 |
Journal: |
Nat Genet |
Title: |
Dual function NFI factors control fetal hemoglobin silencing in adult erythroid cells. |
Volume: |
54 |
Issue: |
6 |
Pages: |
874-884 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
168
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
96
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
274
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Publication |
First Author: |
Mermod N |
Year: |
1989 |
Journal: |
Cell |
Title: |
The proline-rich transcriptional activator of CTF/NF-I is distinct from the replication and DNA binding domain. |
Volume: |
58 |
Issue: |
4 |
Pages: |
741-53 |
|
•
•
•
•
•
|
Publication |
First Author: |
Alevizopoulos A |
Year: |
1995 |
Journal: |
Genes Dev |
Title: |
A proline-rich TGF-beta-responsive transcriptional activator interacts with histone H3. |
Volume: |
9 |
Issue: |
24 |
Pages: |
3051-66 |
|
•
•
•
•
•
|
Publication |
First Author: |
Rupp RA |
Year: |
1990 |
Journal: |
Nucleic Acids Res |
Title: |
Chicken NFI/TGGCA proteins are encoded by at least three independent genes: NFI-A, NFI-B and NFI-C with homologues in mammalian genomes. |
Volume: |
18 |
Issue: |
9 |
Pages: |
2607-16 |
|
•
•
•
•
•
|
Publication |
First Author: |
Nagata K |
Year: |
1982 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Adenovirus DNA replication in vitro: identification of a host factor that stimulates synthesis of the preterminal protein-dCMP complex. |
Volume: |
79 |
Issue: |
21 |
Pages: |
6438-42 |
|
•
•
•
•
•
|
Publication |
First Author: |
Whittle CM |
Year: |
2009 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
DNA-binding specificity and in vivo targets of Caenorhabditis elegans nuclear factor I. |
Volume: |
106 |
Issue: |
29 |
Pages: |
12049-54 |
|
•
•
•
•
•
|
Publication |
First Author: |
Chen KS |
Year: |
2017 |
Journal: |
Cancer Lett |
Title: |
The convergent roles of the nuclear factor I transcription factors in development and cancer. |
Volume: |
410 |
|
Pages: |
124-138 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
Nuclear factor I (NF-I) or CCAAT box-binding transcription factor (CTF) [, , ](also known as TGGCA-binding proteins) are a family of vertebrate nuclear proteins which recognise and bind, as dimers, the palindromic DNA sequence 5'-TGGCANNNTGCCA-3'. This family was first described for its role in stimulating the initiation of adenovirus DNA replication []. In vertebrates there are four members NFIA, NFIB, NFIC, and NFIX and an orthologue from Caenorhabditis elegans has been described, called Nuclear factor I family protein (NFI-I) []. The CTF/NF-I proteins are individually capable of activating transcription and DNA replication, thus they function by regulating cell proliferation and differentiation. They are involved in normal development and have been associated with developmental abnormalities and cancer in humans []. In a given species, there are a large number of different CTF/NF-I proteins, generated both by alternative splicing and by the occurrence of four different genes. CTF/NF-1 proteins contain 400 to 600 amino acids. The N-terminal 200 amino-acid sequence, almost perfectly conserved in all species and genes sequenced, mediates site-specific DNA recognition, protein dimerisation and Adenovirus DNA replication. The C-terminal 100 amino acids contain the transcriptional activation domain. This activation domain is the target of gene expression regulatory pathways elicited by growth factors and it interacts with basal transcription factors and with histone H3 []. |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
Nuclear factor I (NF-I) or CCAAT box-binding transcription factor (CTF) [, , ](also known as TGGCA-binding proteins) are a family of vertebrate nuclear proteins which recognise and bind, as dimers, the palindromic DNA sequence 5'-TGGCANNNTGCCA-3'. This family was first described for its role in stimulating the initiation of adenovirus DNA replication []. In vertebrates there are four members NFIA, NFIB, NFIC, and NFIX and an orthologue from Caenorhabditis elegans has been described, called Nuclear factor I family protein (NFI-I) []. The CTF/NF-I proteins are individually capable of activating transcription and DNA replication, thus they function by regulating cell proliferation and differentiation. They are involved in normal development and have been associated with developmental abnormalities and cancer in humans []. In a given species, there are a large number of different CTF/NF-I proteins, generated both by alternative splicing and by the occurrence of four different genes. CTF/NF-1 proteins contain 400 to 600 amino acids. The N-terminal 200 amino-acid sequence, almost perfectly conserved in all species and genes sequenced, mediates site-specific DNA recognition, protein dimerisation and Adenovirus DNA replication. The C-terminal 100 amino acids contain the transcriptional activation domain. This activation domain is the target of gene expression regulatory pathways elicited by growth factors and it interacts with basal transcription factors and with histone H3 [].This entry represents the 200 amino-acid DNA-binding domain found in N-terminal of CTF/NF1 proteins. It mediates site-specific DNA recognition, protein dimerisation and Adenovirus DNA replication. The CTF/NF-I DNA-binding domain contains four conserved Cys residues, which are required for its DNA-binding activity []. |
|
•
•
•
•
•
|
Publication |
First Author: |
Sakai-Takemura F |
Year: |
2018 |
Journal: |
Sci Rep |
Title: |
Premyogenic progenitors derived from human pluripotent stem cells expand in floating culture and differentiate into transplantable myogenic progenitors. |
Volume: |
8 |
Issue: |
1 |
Pages: |
6555 |
|
•
•
•
•
•
|
Publication |
First Author: |
Plachez C |
Year: |
2008 |
Journal: |
J Comp Neurol |
Title: |
Nuclear factor I gene expression in the developing forebrain. |
Volume: |
508 |
Issue: |
3 |
Pages: |
385-401 |
|
•
•
•
•
•
|
Publication |
First Author: |
Shu T |
Year: |
2003 |
Journal: |
J Neurosci |
Title: |
Abnormal development of forebrain midline glia and commissural projections in Nfia knock-out mice. |
Volume: |
23 |
Issue: |
1 |
Pages: |
203-12 |
|
•
•
•
•
•
|
Publication |
First Author: |
Deák F |
Year: |
2014 |
Journal: |
J Cell Sci |
Title: |
Extracellular deposition of matrilin-2 controls the timing of the myogenic program during muscle regeneration. |
Volume: |
127 |
Issue: |
Pt 15 |
Pages: |
3240-56 |
|
•
•
•
•
•
|
Publication |
First Author: |
Plachez C |
Year: |
2012 |
Journal: |
J Comp Neurol |
Title: |
Expression of nuclear factor one A and -B in the olfactory bulb. |
Volume: |
520 |
Issue: |
14 |
Pages: |
3135-49 |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Nfia/Nfia Nfib/Nfib Nfix/Nfix Tg(Chx10-EGFP/cre,-ALPP)2Clc/? |
Background: |
involves: 129S4/SvJae * C57BL/6N * SJL |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Nfia/Nfia<+> Nfib/Nfib<+> Nfix/Nfix<+> Tg(Chx10-EGFP/cre,-ALPP)2Clc/? |
Background: |
involves: 129S4/SvJae * C57BL/6N * SJL |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Publication |
First Author: |
Novak A |
Year: |
1992 |
Journal: |
J Biol Chem |
Title: |
Four conserved cysteine residues are required for the DNA binding activity of nuclear factor I. |
Volume: |
267 |
Issue: |
18 |
Pages: |
12986-90 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
570
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
488
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
532
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
439
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
532
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
420
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
493
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
391
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
569
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
420
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
439
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
428
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
507
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
175
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
380
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
461
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
488
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
455
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
492
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
498
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
494
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
225
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
487
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
406
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
174
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
269
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
486
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
560
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
Nuclear factor I (NF-I) or CCAAT box-binding transcription factor (CTF) [, , ](also known as TGGCA-binding proteins) are a family of vertebrate nuclear proteins which recognise and bind, as dimers, the palindromic DNA sequence 5'-TGGCANNNTGCCA-3'. This family was first described for its role in stimulating the initiation of adenovirus DNA replication []. In vertebrates there are four members NFIA, NFIB, NFIC, and NFIX and an orthologue from Caenorhabditis elegans has been described, called Nuclear factor I family protein (NFI-I) []. The CTF/NF-I proteins are individually capable of activating transcription and DNA replication, thus they function by regulating cell proliferation and differentiation. They are involved in normal development and have been associated with developmental abnormalities and cancer in humans []. In a given species, there are a large number of different CTF/NF-I proteins, generated both by alternative splicing and by the occurrence of four different genes. CTF/NF-1 proteins contain 400 to 600 amino acids. The N-terminal 200 amino-acid sequence, almost perfectly conserved in all species and genes sequenced, mediates site-specific DNA recognition, protein dimerisation and Adenovirus DNAreplication. The C-terminal 100 amino acids contain the transcriptional activation domain. This activation domain is the target of gene expression regulatory pathways elicited by growth factors and it interacts with basal transcription factors and with histone H3 [].This entry represents the N terminus, of which 200 residues contain the DNA-binding and dimerisation domain, but also has an 8-47 residue highly conserved region 5' of this, whose function is not known. Deletion of the N-terminal 200 amino acids removes the DNA-binding activity, dimerisation-ability and the stimulation of adenovirus DNA replication []. |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Conserved_site |
Description: |
Nuclear factor I (NF-I) or CCAAT box-binding transcription factor (CTF) [, , ](also known as TGGCA-binding proteins) are a family of vertebrate nuclear proteins which recognise and bind, as dimers, the palindromic DNA sequence 5'-TGGCANNNTGCCA-3'. This family was first described for its role in stimulating the initiation of adenovirus DNA replication []. In vertebrates there are four members NFIA, NFIB, NFIC, and NFIX and an orthologue from Caenorhabditis elegans has been described, called Nuclear factor I family protein (NFI-I) []. The CTF/NF-I proteins are individually capable of activating transcription and DNA replication, thus they function by regulating cell proliferation and differentiation. They are involved in normal development and have been associated with developmental abnormalities and cancer in humans []. In a given species, there are a large number of different CTF/NF-I proteins, generated both by alternative splicing and by the occurrence of four different genes. CTF/NF-1 proteins contain 400 to 600 amino acids. The N-terminal 200 amino-acid sequence, almost perfectly conserved in all species and genes sequenced, mediates site-specific DNA recognition, protein dimerisation and Adenovirus DNA replication. The C-terminal 100 amino acids contain the transcriptional activation domain. This activation domain is the target of gene expression regulatory pathways elicited by growth factors and it interacts with basal transcription factors and with histone H3 [].This entry represents a specific signature for this family of proteins, which includes the four vertebrate members NFIA, NFIB, NFIC and NFIX. The signature is a perfectly conserved, highly charged 12-residue peptide located in the DNA-binding domain of CTF/NF-I. It does not contain the four conserved Cys residues, which are required for its DNA-binding activity []. |
|
•
•
•
•
•
|
Publication |
First Author: |
Keeley PW |
Year: |
2023 |
Journal: |
J Neurosci |
Title: |
Nfia Is Critical for AII Amacrine Cell Production: Selective Bipolar Cell Dependencies and Diminished ERG. |
Volume: |
43 |
Issue: |
49 |
Pages: |
8367-8384 |
|
•
•
•
•
•
|
Publication |
First Author: |
The Gene Expression Nervous System Atlas (GENSAT) Project, The Rockefeller University (New York, NY) |
Year: |
2005 |
Journal: |
Database Download |
Title: |
MGI download of GENSAT transgene data |
|
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•
•
•
•
•
|