Entry - *614536 - SWIM-TYPE ZINC FINGER DOMAIN-CONTAINING PROTEIN 7-ASSOCIATED PROTEIN 1; SWSAP1 - OMIM
 
* 614536

SWIM-TYPE ZINC FINGER DOMAIN-CONTAINING PROTEIN 7-ASSOCIATED PROTEIN 1; SWSAP1


Alternative titles; symbols

SWS1-ASSOCIATED PROTEIN 1
ZSWIM7-ASSOCIATED PROTEIN 1; ZSWIM7AP1
CHROMOSOME 19 OPEN READING FRAME 39; C19ORF39


HGNC Approved Gene Symbol: SWSAP1

Cytogenetic location: 19p13.2     Genomic coordinates (GRCh38): 19:11,374,666-11,376,169 (from NCBI)


TEXT

Description

Homologous recombination repair is a well-conserved cellular process for the repair of DNA lesions that uses the intact sister chromatid as a template. SWSAP1 forms a heterodimer with SWS1 (ZSWIM7; 614535) that functions in homologous recombination repair (Liu et al., 2011).


Cloning and Expression

By PCR, Liu et al. (2011) cloned human SWSAP1. The deduced 229-amino acid protein contains Walker A and Walker B nucleotide-binding boxes in its N-terminal half, suggesting that it functions as an ATPase.


Gene Function

Liu et al. (2011) found that SWSAP1 affinity purified with SWS1 from HEK293T cells. The heterodimeric SWS1-SWSAP1 complex had an apparent molecular mass of about 40 kD. Expression of either epitope-tagged SWSAP1 or SWS1 was enhanced upon coexpression. Conversely, knockdown of either SWS1 or SWSAP1 expression via small interfering RNA led to a dramatic decrease in the level of the other protein. SWSAP1 or the SWSAP1-SWS1 complex hydrolyzed ATP in vitro, and activity was significantly increased in the presence of single-stranded DNA compared with double-stranded DNA. SWSAP1 or the SWS1-SWSAP1 complex, but not SWS1 alone, bound DNA in an ATP-independent manner. Knockdown of SWS1 or SWSAP1 increased cell sensitivity to the DNA damaging agent methylmethane sulfonate (MMS) and reduced RAD51 (see 179617) foci formation. Double knockdown of SWSAP1 and RAD51C (602774) further increased MMS sensitivity and further reduced RAD51 foci formation compared with SWSAP1 or RAD51C single-knockdown cells, indicating that SWS1-SWSAP1 and RAD51 likely represent independent subpathways of homologous recombination.


Mapping

Hartz (2012) mapped the SWSAP1 gene to chromosome 19p13.2 based on an alignment of the SWSAP1 sequence (GenBank AK092438) with the genomic sequence (GRCh37).


REFERENCES

  1. Hartz, P. A. Personal Communication. Baltimore, Md. 3/14/2012.

  2. Liu, T., Wan, L., Wu, Y., Chen, J., Huang, J. hSWS1-SWSAP1 is an evolutionarily conserved complex required for efficient homologous recombination repair. J. Biol. Chem. 286: 41758-41766, 2011. [PubMed: 21965664, images, related citations] [Full Text]


Creation Date:
Patricia A. Hartz : 3/16/2012
Edit History:
mgross : 03/16/2012

* 614536

SWIM-TYPE ZINC FINGER DOMAIN-CONTAINING PROTEIN 7-ASSOCIATED PROTEIN 1; SWSAP1


Alternative titles; symbols

SWS1-ASSOCIATED PROTEIN 1
ZSWIM7-ASSOCIATED PROTEIN 1; ZSWIM7AP1
CHROMOSOME 19 OPEN READING FRAME 39; C19ORF39


HGNC Approved Gene Symbol: SWSAP1

Cytogenetic location: 19p13.2     Genomic coordinates (GRCh38): 19:11,374,666-11,376,169 (from NCBI)


TEXT

Description

Homologous recombination repair is a well-conserved cellular process for the repair of DNA lesions that uses the intact sister chromatid as a template. SWSAP1 forms a heterodimer with SWS1 (ZSWIM7; 614535) that functions in homologous recombination repair (Liu et al., 2011).


Cloning and Expression

By PCR, Liu et al. (2011) cloned human SWSAP1. The deduced 229-amino acid protein contains Walker A and Walker B nucleotide-binding boxes in its N-terminal half, suggesting that it functions as an ATPase.


Gene Function

Liu et al. (2011) found that SWSAP1 affinity purified with SWS1 from HEK293T cells. The heterodimeric SWS1-SWSAP1 complex had an apparent molecular mass of about 40 kD. Expression of either epitope-tagged SWSAP1 or SWS1 was enhanced upon coexpression. Conversely, knockdown of either SWS1 or SWSAP1 expression via small interfering RNA led to a dramatic decrease in the level of the other protein. SWSAP1 or the SWSAP1-SWS1 complex hydrolyzed ATP in vitro, and activity was significantly increased in the presence of single-stranded DNA compared with double-stranded DNA. SWSAP1 or the SWS1-SWSAP1 complex, but not SWS1 alone, bound DNA in an ATP-independent manner. Knockdown of SWS1 or SWSAP1 increased cell sensitivity to the DNA damaging agent methylmethane sulfonate (MMS) and reduced RAD51 (see 179617) foci formation. Double knockdown of SWSAP1 and RAD51C (602774) further increased MMS sensitivity and further reduced RAD51 foci formation compared with SWSAP1 or RAD51C single-knockdown cells, indicating that SWS1-SWSAP1 and RAD51 likely represent independent subpathways of homologous recombination.


Mapping

Hartz (2012) mapped the SWSAP1 gene to chromosome 19p13.2 based on an alignment of the SWSAP1 sequence (GenBank AK092438) with the genomic sequence (GRCh37).


REFERENCES

  1. Hartz, P. A. Personal Communication. Baltimore, Md. 3/14/2012.

  2. Liu, T., Wan, L., Wu, Y., Chen, J., Huang, J. hSWS1-SWSAP1 is an evolutionarily conserved complex required for efficient homologous recombination repair. J. Biol. Chem. 286: 41758-41766, 2011. [PubMed: 21965664] [Full Text: https://doi.org/10.1074/jbc.M111.271080]


Creation Date:
Patricia A. Hartz : 3/16/2012

Edit History:
mgross : 03/16/2012