Dnase1l2-KO Mouse
Common Name
Dnase1l2-KO
제품 ID
S-KO-11870
Backgroud
C57BL/6JCya
품종 계통계통 ID
KOCMP-66705-Dnase1l2-B6J-VA
상태
이 마우스 계통을 논문에서 사용할 경우, “Dnase1l2-KO Mouse (카탈로그 번호 S-KO-11870)은 Cyagen에서 구입하였습니다.”라고 명시해 주시기 바랍니다.
구매 가능한 제품 종류
연령
Genotype
성별
수량
표준 제공 조건은 최소 3마리의 이형접합(heterozygous) 보균자를 보장합니다. 동형접합(homozygous) 보균자 및/또는 특정 성별에 대한 브리딩 서비스도 제공됩니다.
기본 정보
품종 계통
Dnase1l2-KO
품종 계통계통 ID
KOCMP-66705-Dnase1l2-B6J-VA
유전자명
제품 ID
S-KO-11870
유전자 별칭
4733401H14Rik
배경
C57BL/6JCya
NCBI ID
변형 내용
Conventional knockout
염색체
Chr 17
Phenotype
Datasheet
적용 분야
--
품종 계통 설명
Ensembl 전사체 ID
ENSMUST00000088506
NCBI 전사체 ID
NM_025718
타겟 영역
Exon 2~7
유효 영역 크기
~1.5 kb
유전자 연구 개요
Dnase1l2, or DNase1-like 2, is an endonuclease with metal-dependent endonuclease activity, having a broad pH range with an acidic optimum [2,5]. It plays a crucial role in DNA degradation processes, especially during the terminal differentiation of keratinocytes. This involves the removal of nuclear DNA in the formation of the stratum corneum, hair, nails, and in maintaining innate antimicrobial defense in the epidermis [3,4,8]. It may also be involved in biological processes related to the epithelial-mesenchymal transition [1]. Genetic models, such as knockout mice, have been essential in studying its functions.
In mouse models, inactivation of Dnase1l2 alone or in combination with other nucleases has provided insights into its role. For example, Dnase1l2 -/- mice showed aberrant retention of DNA in hair, nails, tongue, and esophagus epithelia, with the presence of nuclear DNA disturbing the normal arrangement of structural proteins in hair corneocytes and reducing hair's mechanical stress resistance [8]. In Dnase1l2 -/- Dnase2 Δep mice, nuclear DNA was retained in the stratum corneum, leading to parakeratosis, indicating cooperation between Dnase1l2 and Dnase2 in epidermal cornification [6]. Double deficiency of Trex2 and Dnase1l2 led to massive DNA fragment accumulation in the cornified layers of the tongue epithelium without activating inflammatory responses, suggesting their cooperation in lingual keratinocyte cornification [7].
In conclusion, Dnase1l2 is essential for DNA degradation during the terminal differentiation of keratinocytes in various tissues. Studies using gene knockout mouse models have revealed its role in maintaining the normal structure and function of skin appendages, epidermal cornification, and in preventing parakeratosis. Its potential as a carcinogenic marker in breast cancer, as well as its role in cystic fibrosis lung disease treatment and innate antimicrobial defense, highlights its significance in multiple disease areas [1,2,3].
References:
1. Liu, Chang-Rui, Meng, Fan-Hua. 2020. DNASE1L2, as a Carcinogenic Marker, Affects the Phenotype of Breast Cancer Cells Via Regulating Epithelial-Mesenchymal Transition Process. In Cancer biotherapy & radiopharmaceuticals, 36, 180-188. doi:10.1089/cbr.2019.3504. https://pubmed.ncbi.nlm.nih.gov/32343605/
2. Delfino, Danila, Mori, Giulia, Rivetti, Claudio, Pasut, Gianfranco, Percudani, Riccardo. 2021. Actin-Resistant DNase1L2 as a Potential Therapeutics for CF Lung Disease. In Biomolecules, 11, . doi:10.3390/biom11030410. https://pubmed.ncbi.nlm.nih.gov/33802146/
3. Eckhart, L, Fischer, H, Barken, K B, Tolker-Nielsen, T, Tschachler, E. 2007. DNase1L2 suppresses biofilm formation by Pseudomonas aeruginosa and Staphylococcus aureus. In The British journal of dermatology, 156, 1342-5. doi:. https://pubmed.ncbi.nlm.nih.gov/17459041/
4. Fischer, Heinz, Eckhart, Leopold, Mildner, Michael, Ghannadan, Minoo, Tschachler, Erwin. 2006. DNase1L2 degrades nuclear DNA during corneocyte formation. In The Journal of investigative dermatology, 127, 24-30. doi:. https://pubmed.ncbi.nlm.nih.gov/16902420/
5. Mori, Giulia, Delfino, Danila, Pibiri, Paola, Rivetti, Claudio, Percudani, Riccardo. 2022. Origin and significance of the human DNase repertoire. In Scientific reports, 12, 10364. doi:10.1038/s41598-022-14133-w. https://pubmed.ncbi.nlm.nih.gov/35725583/
6. Fischer, Heinz, Buchberger, Maria, Napirei, Markus, Tschachler, Erwin, Eckhart, Leopold. 2017. Inactivation of DNase1L2 and DNase2 in keratinocytes suppresses DNA degradation during epidermal cornification and results in constitutive parakeratosis. In Scientific reports, 7, 6433. doi:10.1038/s41598-017-06652-8. https://pubmed.ncbi.nlm.nih.gov/28743926/
7. Manils, Joan, Fischer, Heinz, Climent, Joan, Eckhart, Leopold, Soler, Concepció. 2017. Double deficiency of Trex2 and DNase1L2 nucleases leads to accumulation of DNA in lingual cornifying keratinocytes without activating inflammatory responses. In Scientific reports, 7, 11902. doi:10.1038/s41598-017-12308-4. https://pubmed.ncbi.nlm.nih.gov/28928425/
8. Fischer, Heinz, Szabo, Sandra, Scherz, Jennifer, Tschachler, Erwin, Eckhart, Leopold. 2011. Essential role of the keratinocyte-specific endonuclease DNase1L2 in the removal of nuclear DNA from hair and nails. In The Journal of investigative dermatology, 131, 1208-15. doi:10.1038/jid.2011.13. https://pubmed.ncbi.nlm.nih.gov/21307874/
품질 관리 기준
정자 검사
동결 보존 전: 정자 농도 측정 및 정자 생존율 평가.
동결 보존 후: 각 배치에서 동결 보존된 정자 바이알 1개를 선택하여 체외수정(in vitro fertilization)에 사용합니다.
Environmental Standards:
SPFAvailable Region:
GlobalSource:
Cyagen문의하기
맞춤형 동물 모델 관련 상담을 위해 Cyagen 전문가와 연락해 보세요. 아래 양식을 작성하여 상담을 시작하거나 견적을 요청하시기 바랍니다.
Cyagen은 고객님의 개인정보를 소중히 여깁니다. 최신 제품, 서비스 및 인사이트를 안내드리고자 합니다. 고객님의 수신 설정은 다음과 같습니다:
해당 커뮤니케이션은 언제든지 수신 거부하실 수 있습니다. 수신 거부 방법 및 데이터 보호에 대한 자세한 내용은 개인정보처리방침을 참고해 주시기 바랍니다.
아래 버튼을 클릭함으로써, 요청하신 콘텐츠 제공을 위해 본 양식을 통해 제출된 개인정보를 Cyagen이 저장 및 처리하는 데 동의하게 됩니다.
