Cloning and expression of truncated CTCF
The CTCF gene maps on chromosome 16 at 16q21- q22.3. It encodes a transcriptional factor protein CTCF called zinc finger protein. CTCF has a number of fUnctions in the cell including controls of cell proliferation by having interactions with other proteins. There are several proteins associated w...
Saved in:
| Main Author: | |
|---|---|
| Format: | Article |
| Language: | en |
| Published: |
Pusat Pengajian Sains Kesihatan, Universiti Sains Malaysia
2005
|
| Subjects: | |
| Online Access: | http://eprints.usm.my/47200/1/PTA...Chot%20San%20Ngan...2005...-24%20pages.pdf http://eprints.usm.my/47200/ |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| _version_ | 1834503792404463616 |
|---|---|
| author | Ngan, Chot San |
| author_facet | Ngan, Chot San |
| author_sort | Ngan, Chot San |
| building | Hamzah Sendut Library |
| collection | Institutional Repository |
| content_provider | Universiti Sains Malaysia |
| content_source | USM Institutional Repository |
| continent | Asia |
| country | Malaysia |
| description | The CTCF gene maps on chromosome 16 at 16q21- q22.3. It encodes a transcriptional
factor protein CTCF called zinc finger protein. CTCF has a number of fUnctions in the
cell including controls of cell proliferation by having interactions with other proteins.
There are several proteins associated with CTCF. Among them are proteins involved in
transcriptional and cell proliferation control, RNA processing, signal transduction,
nucleosome components and tumor suppressors.
CTCF consists of N-terminal domain, zmc finger domain and C-terminal domain.
Extensive research have been done to elucidate the important regions that might play
important role in both DNA binding and protein-protein interactions. Previous studies has
shown there was a region in the C-domain which has direct interaction with large subunit
of RNA polymerase II and controlling various cellular process.
In this study, a tnmcated CTCF from the C-terminal domain was produced by polymerase
chain reaction (PCR). The amplified products was then subcloned into the intermediate
cloning vector, pTOP02.1 and transformed into E. coli strain DH5 a. The insert was then
cut with respective restriction enzyme to obtain the truncated region and further ligated
into pETI6b expression vector for its expression in E. coli strain BL21 (DE3). Expressed
protein was separated using SDS-PAGE followed by Western Blotting using a-Histag
monoclonal antibody. The truncated CTCF protein was detected to migrate at the size ofapproximately 27kDa despite its theoretical size of 4kDa. This migration was expected
and due to anomalous conformational changes during migration. |
| format | Article |
| id | my.usm.eprints.47200 |
| institution | Universiti Sains Malaysia |
| language | en |
| publishDate | 2005 |
| publisher | Pusat Pengajian Sains Kesihatan, Universiti Sains Malaysia |
| record_format | eprints |
| spelling | my.usm.eprints.47200 http://eprints.usm.my/47200/ Cloning and expression of truncated CTCF Ngan, Chot San R Medicine (General) The CTCF gene maps on chromosome 16 at 16q21- q22.3. It encodes a transcriptional factor protein CTCF called zinc finger protein. CTCF has a number of fUnctions in the cell including controls of cell proliferation by having interactions with other proteins. There are several proteins associated with CTCF. Among them are proteins involved in transcriptional and cell proliferation control, RNA processing, signal transduction, nucleosome components and tumor suppressors. CTCF consists of N-terminal domain, zmc finger domain and C-terminal domain. Extensive research have been done to elucidate the important regions that might play important role in both DNA binding and protein-protein interactions. Previous studies has shown there was a region in the C-domain which has direct interaction with large subunit of RNA polymerase II and controlling various cellular process. In this study, a tnmcated CTCF from the C-terminal domain was produced by polymerase chain reaction (PCR). The amplified products was then subcloned into the intermediate cloning vector, pTOP02.1 and transformed into E. coli strain DH5 a. The insert was then cut with respective restriction enzyme to obtain the truncated region and further ligated into pETI6b expression vector for its expression in E. coli strain BL21 (DE3). Expressed protein was separated using SDS-PAGE followed by Western Blotting using a-Histag monoclonal antibody. The truncated CTCF protein was detected to migrate at the size ofapproximately 27kDa despite its theoretical size of 4kDa. This migration was expected and due to anomalous conformational changes during migration. Pusat Pengajian Sains Kesihatan, Universiti Sains Malaysia 2005 Article NonPeerReviewed application/pdf en http://eprints.usm.my/47200/1/PTA...Chot%20San%20Ngan...2005...-24%20pages.pdf Ngan, Chot San (2005) Cloning and expression of truncated CTCF. approximately 27kDa despite its theoretical size of 4kDa. This migration was expected and due to anomalous conformational changes during migration.. (Submitted) |
| spellingShingle | R Medicine (General) Ngan, Chot San Cloning and expression of truncated CTCF |
| title | Cloning and expression of truncated
CTCF |
| title_full | Cloning and expression of truncated
CTCF |
| title_fullStr | Cloning and expression of truncated
CTCF |
| title_full_unstemmed | Cloning and expression of truncated
CTCF |
| title_short | Cloning and expression of truncated
CTCF |
| title_sort | cloning and expression of truncated
ctcf |
| topic | R Medicine (General) |
| url | http://eprints.usm.my/47200/1/PTA...Chot%20San%20Ngan...2005...-24%20pages.pdf http://eprints.usm.my/47200/ |
| url_provider | http://eprints.usm.my/ |