Type |
Details |
Score |
Strain |
Attribute String: |
targeted mutation, mutant strain, congenic |
|
•
•
•
•
•
|
Strain |
Attribute String: |
congenic, mutant strain, targeted mutation |
|
•
•
•
•
•
|
Strain |
Attribute String: |
mutant strain, coisogenic, targeted mutation |
|
•
•
•
•
•
|
Strain |
Attribute String: |
mutant strain, coisogenic, targeted mutation |
|
•
•
•
•
•
|
Strain |
Attribute String: |
congenic, mutant strain, targeted mutation |
|
•
•
•
•
•
|
Strain |
Attribute String: |
targeted mutation, mutant strain, congenic |
|
•
•
•
•
•
|
Strain |
Attribute String: |
mutant strain, targeted mutation, congenic |
|
•
•
•
•
•
|
Strain |
Attribute String: |
targeted mutation, congenic, mutant strain |
|
•
•
•
•
•
|
Strain |
Attribute String: |
coisogenic, endonuclease-mediated mutation, mutant strain |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 |
Background: |
either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6) |
Zygosity: |
hm |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 |
Background: |
involves: 129S7/SvEvBrd * C57BL/6 |
Zygosity: |
hm |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 |
Background: |
involves: 129S7/SvEvBrd |
Zygosity: |
hm |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rint1/Rint1<+> |
Background: |
Not Specified |
Zygosity: |
ht |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 |
Background: |
involves: 129S7/SvEvBrd |
Zygosity: |
hm |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 |
Background: |
involves: 129S6/SvEvTac * C3H * C57BL/6 |
Zygosity: |
hm |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 |
Background: |
B6.129S6-Rad50 |
Zygosity: |
hm |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 |
Background: |
B6.129S6-Rad50 |
Zygosity: |
hm |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 |
Background: |
B6.129S6-Rad50 |
Zygosity: |
hm |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rint1/Rint1<+> |
Background: |
C57BL/6N-Rint1/J |
Zygosity: |
ht |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rint1/Rint1 Tg(Pax6-cre,GFP)2Pgr/? |
Background: |
involves: 129P2/OlaHsd |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Publication |
First Author: |
Grigaravicius P |
Year: |
2016 |
Journal: |
Cell Death Differ |
Title: |
Rint1 inactivation triggers genomic instability, ER stress and autophagy inhibition in the brain. |
Volume: |
23 |
Issue: |
3 |
Pages: |
454-68 |
|
•
•
•
•
•
|
Publication |
First Author: |
Carney JP |
Year: |
1998 |
Journal: |
Cell |
Title: |
The hMre11/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response. |
Volume: |
93 |
Issue: |
3 |
Pages: |
477-86 |
|
•
•
•
•
•
|
Publication |
First Author: |
Ciapponi L |
Year: |
2004 |
Journal: |
Curr Biol |
Title: |
The Drosophila Mre11/Rad50 complex is required to prevent both telomeric fusion and chromosome breakage. |
Volume: |
14 |
Issue: |
15 |
Pages: |
1360-6 |
|
•
•
•
•
•
|
Publication |
First Author: |
Trujillo KM |
Year: |
2001 |
Journal: |
J Biol Chem |
Title: |
DNA structure-specific nuclease activities in the Saccharomyces cerevisiae Rad50*Mre11 complex. |
Volume: |
276 |
Issue: |
38 |
Pages: |
35458-64 |
|
•
•
•
•
•
|
Publication |
First Author: |
Berardinelli F |
Year: |
2014 |
Journal: |
Int J Radiat Biol |
Title: |
Radiation-induced telomere length variations in normal and in Nijmegen Breakage Syndrome cells. |
Volume: |
90 |
Issue: |
1 |
Pages: |
45-52 |
|
•
•
•
•
•
|
Publication |
First Author: |
Yin Y |
Year: |
2013 |
Journal: |
Mol Cell Biol |
Title: |
Impaired resection of meiotic double-strand breaks channels repair to nonhomologous end joining in Caenorhabditis elegans. |
Volume: |
33 |
Issue: |
14 |
Pages: |
2732-47 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
RAD50 is involved in DNA double-strand break repair (DSBR), telomere maintenance and meiotic recombination [, , ]. The RAD50/MRE11 complex possesses single-strand endonuclease activity and ATP-dependent double-strand-specific exonuclease activity [, ]. RAD50 provides ATP-dependent control of Mre11 by unwinding and/or repositioning DNA ends into the MRE11 active site [, , ]. This entry represents the eukaryotic Rad50 that is distantly related to the SbcC family of bacterial proteins.In Saccharomyces cerevisiae, Rad50 forms the MRX complex with Mre11 and Xrs2. In humans, RAD50 forms the MRN complex with MRE11 and NBN (also known as NBS1). Mutations in the RAD50 gene cause the Nijmegen breakage syndrome-like disorder (NBSLD) []. The genetic variations in the RAD50 gene have been linked to susceptibility to asthma []. |
|
•
•
•
•
•
|
Publication |
First Author: |
Oikarinen SI |
Year: |
2009 |
Journal: |
Carcinogenesis |
Title: |
Genetic mapping of Mom5, a novel modifier of Apc(Min)-induced intestinal tumorigenesis. |
Volume: |
30 |
Issue: |
9 |
Pages: |
1591-6 |
|
•
•
•
•
•
|
Publication |
First Author: |
Paull TT |
Year: |
1998 |
Journal: |
Mol Cell |
Title: |
The 3' to 5' exonuclease activity of Mre 11 facilitates repair of DNA double-strand breaks. |
Volume: |
1 |
Issue: |
7 |
Pages: |
969-79 |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Nbn/Nbn Rad50/Rad50 |
Background: |
involves: 129S7/SvEvBrd * 129/Sv |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
The Mre11 complex is a multi-subunit nuclease that is composed of Mre11, Rad50 and Nbs1/Xrs2, and is involved in checkpoint signalling and DNA replication []. Mre11 has an intrinsic DNA-binding activity that is stimulated by Rad50 on its own or in combination with Nbs1 []. |
|
•
•
•
•
•
|
Strain |
Attribute String: |
congenic, mutant strain, targeted mutation |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 Trp53/Trp53 |
Background: |
involves: 129S2/SvPas * 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Mre11a/Mre11a Rad50/Rad50 |
Background: |
involves: 129S7/SvEvBrd * C57BL/6 |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 |
Background: |
involves: 129S7/SvEvBrd * C57BL/6 |
Zygosity: |
ht |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Atm/Atm Rad50/Rad50 |
Background: |
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Atm/Atm<+> Rad50/Rad50 |
Background: |
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Nbn/Nbn Rad50/Rad50 |
Background: |
involves: 129S7/SvEvBrd * C57BL/6 |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Nbn/Nbn<+> Rad50/Rad50 |
Background: |
involves: 129S7/SvEvBrd * C57BL/6 |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 Tg(BCL2)22Wehi/? |
Background: |
involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6JWehi * SJL/JWehi |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Chek2/Chek2 Rad50/Rad50 |
Background: |
involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Chek2/Chek2<+> Rad50/Rad50 |
Background: |
involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 Smc1a/Smc1a |
Background: |
involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6 |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Nbn/Nbn<+> Rad50/Rad50 |
Background: |
involves: 129S7/SvEvBrd * 129/Sv |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50<+> |
Background: |
involves: 129/Sv * C57BL/6 |
Zygosity: |
ht |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50<+> |
Background: |
involves: 129/Sv * C57BL/6 |
Zygosity: |
ht |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 |
Background: |
involves: 129/Sv * 129S7/SvEvBrd * C57BL/6 |
Zygosity: |
ht |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50<+> |
Background: |
involves: 129/Sv * C57BL/6 |
Zygosity: |
ht |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rint1/Rint1 Tg(Pax6-cre,GFP)2Pgr/? Trp53/Trp53 |
Background: |
involves: 129P2/OlaHsd |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Publication |
First Author: |
Paull TT |
Year: |
2000 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
A mechanistic basis for Mre11-directed DNA joining at microhomologies. |
Volume: |
97 |
Issue: |
12 |
Pages: |
6409-14 |
|
•
•
•
•
•
|
Publication |
First Author: |
D'Amours D |
Year: |
2002 |
Journal: |
Nat Rev Mol Cell Biol |
Title: |
The Mre11 complex: at the crossroads of dna repair and checkpoint signalling. |
Volume: |
3 |
Issue: |
5 |
Pages: |
317-27 |
|
•
•
•
•
•
|
Publication |
First Author: |
Schiller CB |
Year: |
2012 |
Journal: |
Nat Struct Mol Biol |
Title: |
Structure of Mre11-Nbs1 complex yields insights into ataxia-telangiectasia-like disease mutations and DNA damage signaling. |
Volume: |
19 |
Issue: |
7 |
Pages: |
693-700 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Homologous_superfamily |
Description: |
The Mre11 complex is a multi-subunit nuclease that is composed of Mre11, Rad50 and Nbs1/Xrs2, and is involved in checkpoint signalling and DNA replication []. Mre11 has an intrinsic DNA-binding activity that is stimulated by Rad50 on its own or in combination with Nbs1 [].Mre11 dimerizes via phosphodiesterase domains flanked by a alpha/beta capping domain, process which creates a U-shaped particle with a broad DNA/Rad50 binding cleft []. This superfamily represents the Mre11 capping domain. |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
The catalytic domains of Rad50 are similar to the ATP-binding cassette of ABC transporters, but are not associated with membrane-spanning domains. The conserved ATP-binding motifs common to Rad50 and the ABC transporter family include the Walker A and Walker B motifs, the Q loop, a histidine residue in the switch region, a D-loop, and a conserved LSGG sequence. This conserved sequence, LSGG, is the most specific and characteristic motif of this family and is thus known as the ABC signature sequence []. |
|
•
•
•
•
•
|
Publication |
First Author: |
Kafer GR |
Year: |
2020 |
Journal: |
Front Cell Dev Biol |
Title: |
A Survey of Essential Genome Stability Genes Reveals That Replication Stress Mitigation Is Critical for Peri-Implantation Embryogenesis. |
Volume: |
8 |
|
Pages: |
416 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
261
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
486
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Mre11a/Mre11a<+> Rad50/Rad50 |
Background: |
involves: 129S7/SvEvBrd * C57BL/6 |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 Tg(Mx1-cre)1Cgn/? |
Background: |
involves: 129S7/SvEvBrd * C57BL/6 * CBA |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 Tg(Pcp2-cre)2Mpin/? |
Background: |
involves: 129S7/SvEvBrd * C57BL/6 |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 Tg(Cd4-cre)1Cwi/? |
Background: |
involves: 129S6/SvEvTac * C57BL/6 * DBA/2 |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Atm/Atm Rad50/Rad50<+> |
Background: |
involves: 129/Sv * 129S6/SvEvTac * C57BL/6 |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50<+> Spo11/Spo11 |
Background: |
involves: 129/Sv * C57BL/6 |
Zygosity: |
cx |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
170
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Domain |
Description: |
This AAA domain is found in a group of uncharacterised proteins, including YhaN from Bacillus subtilis and DNA double-strand break repair Rad50 ATPase from Archaeoglobus fulgidus.AAA ATPases belong to the AAA+ superfamily of ringshaped P-loop NTPases, which exert their activity through the energy-dependent unfolding of macromolecules []. |
|
•
•
•
•
•
|
Allele |
Name: |
transgene insertion 1, Edward M Rubin |
Allele Type: |
Transgenic |
Attribute String: |
Inserted expressed sequence |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> Rad50/Rad50 |
Background: |
involves: 129/Sv * C57BL/6 |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Genotype |
Symbol: |
Rad50/Rad50 Gt(ROSA)26Sor/Gt(ROSA)26Sor<+> |
Background: |
involves: 129/Sv * C57BL/6 |
Zygosity: |
cn |
Has Mutant Allele: |
true |
|
•
•
•
•
•
|
Publication |
First Author: |
Johzuka K |
Year: |
1995 |
Journal: |
Genetics |
Title: |
Interaction of Mre11 and Rad50: two proteins required for DNA repair and meiosis-specific double-strand break formation in Saccharomyces cerevisiae. |
Volume: |
139 |
Issue: |
4 |
Pages: |
1521-32 |
|
•
•
•
•
•
|
Publication |
First Author: |
Tavassoli M |
Year: |
1995 |
Journal: |
Nucleic Acids Res |
Title: |
Cloning and characterisation of the Schizosaccharomyces pombe rad32 gene: a gene required for repair of double strand breaks and recombination. |
Volume: |
23 |
Issue: |
3 |
Pages: |
383-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Furuse M |
Year: |
1998 |
Journal: |
EMBO J |
Title: |
Distinct roles of two separable in vitro activities of yeast Mre11 in mitotic and meiotic recombination. |
Volume: |
17 |
Issue: |
21 |
Pages: |
6412-25 |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
Mre11 and Rad50 are two proteins required for DNA repair and meiosis-specific double-strand break formation in Saccharomyces cerevisiae. Mre11 by itself has 3' to 5' exonuclease activity that is increased when Mre11 is in a complex with Rad50 []. These eukaryotic proteins contain one metallo-phosphoesterase domain followed by an Mre11 DNA-binding domain. S. cerevisiae Mre11 is required for DNA repair and meiosis-specificdouble-strand break (DSB) formation []and has both 3' to 5' exonuclease activity (whichincreases when in complex with Rad50) and endonuclease activity. The N-terminal phosphoesterase domain isrequired for DSB repair, and the carboxyl-terminal dsDNA-binding domain is essential during meiosis forchromatin modification and DSB formation []. Schizosaccharomyces pombe rad32 is required for repair of double strand breaks and recombination []. |
|
•
•
•
•
•
|
Publication |
First Author: |
Trujillo KM |
Year: |
1998 |
Journal: |
J Biol Chem |
Title: |
Nuclease activities in a complex of human recombination and DNA repair factors Rad50, Mre11, and p95. |
Volume: |
273 |
Issue: |
34 |
Pages: |
21447-50 |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
706
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
513
 |
Fragment?: |
true |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
706
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
679
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
This entry represents a small group of nuclease SbcCD subunit C (SbcC) proteins, mainly from gammaproteobacteria. SbcC are known are part of an exonuclease complex with sbcD homologues. SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'->5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity [].The entry also includes a small number of proteins annotated as probable DNA double-strand break repair Rad50 ATPase, but which are experimentally uncharacterised. |
|
•
•
•
•
•
|
Publication |
First Author: |
Kim JH |
Year: |
2017 |
Journal: |
Cell Rep |
Title: |
The Mre11-Nbs1 Interface Is Essential for Viability and Tumor Suppression. |
Volume: |
18 |
Issue: |
2 |
Pages: |
496-507 |
|
•
•
•
•
•
|
Publication |
First Author: |
Lee GR |
Year: |
2003 |
Journal: |
Immunity |
Title: |
Regulation of the Th2 cytokine locus by a locus control region. |
Volume: |
19 |
Issue: |
1 |
Pages: |
145-53 |
|
•
•
•
•
•
|
Publication |
First Author: |
van den Bosch M |
Year: |
2003 |
Journal: |
EMBO Rep |
Title: |
The MRN complex: coordinating and mediating the response to broken chromosomes. |
Volume: |
4 |
Issue: |
9 |
Pages: |
844-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
de Jager M |
Year: |
2001 |
Journal: |
Mol Cell |
Title: |
Human Rad50/Mre11 is a flexible complex that can tether DNA ends. |
Volume: |
8 |
Issue: |
5 |
Pages: |
1129-35 |
|
•
•
•
•
•
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Protein Domain |
Type: |
Domain |
Description: |
The MRN complex (Mre11-Rad50-Nbs1) plays an important role in many DNA metabolic events that involve DNA double-stranded breaks. MRN is one of the first factors to be localised to DNA lesions where it might have a structural role by tethering and stabilising broken chromosomes [, ]. Rad50 is a split ABC-type ATPase; its centre contains a long heptad repeat that folds into an antiparallel coiled coil, bringing the N-terminal (Walker A) and the C-terminal (Walker B) domains in close proximity []. The apex of the coiled coil contains a dimerization interface, a conserved Cys-X-X-Cys motif in a hook-shaped domain that dimerizes with a second hook domain via cysteine-mediated zinc ion coordination. This zinc dependent dimerization event allows the formation of a complex that has appropriate lengths and conformational proporties to link sister chromatids in homologous recombination and DNA ends in non-homologous end-joining. |
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Strain |
Attribute String: |
deletion, mutant stock, transgenic, targeted mutation |
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Genotype |
Symbol: |
Del(11Irf1-D11Mit23)1Rub/Del(11Irf1-D11Mit23)1Rub Tg(A94G6)1Rub/? |
Background: |
involves: 129S6/SvEvTac * C57BL/6J |
Zygosity: |
cx |
Has Mutant Allele: |
true |
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Publication |
First Author: |
Collin GB |
Year: |
2012 |
Journal: |
PLoS One |
Title: |
The Alström syndrome protein, ALMS1, interacts with α-actinin and components of the endosome recycling pathway. |
Volume: |
7 |
Issue: |
5 |
Pages: |
e37925 |
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Publication |
First Author: |
Loseva EF |
Year: |
2000 |
Journal: |
Genetika |
Title: |
[Cloning of a new murine gene coding for a protein immunologically related to RecA protein from Escherichia coli]. |
Volume: |
36 |
Issue: |
5 |
Pages: |
613-21 |
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Publication |
First Author: |
Nairz K |
Year: |
1997 |
Journal: |
Genes Dev |
Title: |
mre11S--a yeast mutation that blocks double-strand-break processing and permits nonhomologous synapsis in meiosis. |
Volume: |
11 |
Issue: |
17 |
Pages: |
2272-90 |
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Publication |
First Author: |
Chamankhah M |
Year: |
1998 |
Journal: |
Gene |
Title: |
Isolation of hMRE11B: failure to complement yeast mre11 defects due to species-specific protein interactions. |
Volume: |
225 |
Issue: |
1-2 |
Pages: |
107-16 |
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Publication |
First Author: |
Yang YG |
Year: |
2006 |
Journal: |
EMBO J |
Title: |
Conditional deletion of Nbs1 in murine cells reveals its role in branching repair pathways of DNA double-strand breaks. |
Volume: |
25 |
Issue: |
23 |
Pages: |
5527-38 |
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Publication |
First Author: |
Solaimani P |
Year: |
2013 |
Journal: |
Toxicol Sci |
Title: |
Genome-wide RNAi high-throughput screen identifies proteins necessary for the AHR-dependent induction of CYP1A1 by 2,3,7,8-tetrachlorodibenzo-p-dioxin. |
Volume: |
136 |
Issue: |
1 |
Pages: |
107-19 |
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Publication |
First Author: |
Chen Z |
Year: |
2007 |
Journal: |
J Bacteriol |
Title: |
The sbcDC locus mediates repression of type 5 capsule production as part of the SOS response in Staphylococcus aureus. |
Volume: |
189 |
Issue: |
20 |
Pages: |
7343-50 |
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Publication |
First Author: |
Sweet DJ |
Year: |
1993 |
Journal: |
EMBO J |
Title: |
The TIP1 gene of Saccharomyces cerevisiae encodes an 80 kDa cytoplasmic protein that interacts with the cytoplasmic domain of Sec20p. |
Volume: |
12 |
Issue: |
7 |
Pages: |
2831-40 |
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Publication |
First Author: |
Xiao J |
Year: |
2001 |
Journal: |
J Biol Chem |
Title: |
RINT-1, a novel Rad50-interacting protein, participates in radiation-induced G(2)/M checkpoint control. |
Volume: |
276 |
Issue: |
9 |
Pages: |
6105-11 |
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Publication |
First Author: |
Kong LJ |
Year: |
2006 |
Journal: |
Mol Cell |
Title: |
The Rb-related p130 protein controls telomere lengthening through an interaction with a Rad50-interacting protein, RINT-1. |
Volume: |
22 |
Issue: |
1 |
Pages: |
63-71 |
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Publication |
First Author: |
Arasaki K |
Year: |
2006 |
Journal: |
Mol Biol Cell |
Title: |
RINT-1 regulates the localization and entry of ZW10 to the syntaxin 18 complex. |
Volume: |
17 |
Issue: |
6 |
Pages: |
2780-8 |
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Publication |
First Author: |
Li L |
Year: |
2006 |
Journal: |
Plant Cell |
Title: |
MAIGO2 is involved in exit of seed storage proteins from the endoplasmic reticulum in Arabidopsis thaliana. |
Volume: |
18 |
Issue: |
12 |
Pages: |
3535-47 |
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Protein Domain |
Type: |
Family |
Description: |
This entry includes RINT-1 from animals, Tip20 from yeasts and MAIGO2 (Mag2) from plants. They play a role in anterograde transport from the endoplasmic reticulum (ER) to the Golgi and/or retrograde transport from the Golgi to the ER share sequence similarity []. They are part of the CATCHR (complexes associated with tethering containing helical rods) family which comprises the exocyst, COG, GARP, and DSL1 complexes and share a similar structure organisation with an N-terminal coiled-coil and a C-terminal α-helical bundle, which might be a protein-protein interaction module necessary for the formation of functional complexes.RINT-1 interacts with Rad50 only during late S and G2/M phases and participates in radiation induced checkpoint control []. RINT-1 also functions in membrane trafficking from the endoplasmic reticulum (ER) to the Golgi complex in interphase cells [, , ].Tip20 is involved in the retrograde transport from the Golgi to the ER [, ].Arabidopsis Mag2 functions in the transport of storage protein precursors between the ER and Golgi complex in plants [, ]. |
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Publication |
First Author: |
Ding M |
Year: |
2021 |
Journal: |
Front Aging Neurosci |
Title: |
The Essential DNA Damage Response Complex MRN Is Dispensable for the Survival and Function of Purkinje Neurons. |
Volume: |
13 |
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Pages: |
786199 |
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Publication |
First Author: |
Li L |
Year: |
2013 |
Journal: |
Plant J |
Title: |
MAG2 and three MAG2-INTERACTING PROTEINs form an ER-localized complex to facilitate storage protein transport in Arabidopsis thaliana. |
Volume: |
76 |
Issue: |
5 |
Pages: |
781-91 |
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