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Literature DB >> 18322011

Does antisense make sense of AID targeting?

Sergio Roa¹, Fei Li Kuang, Matthew D Scharff.

Abstract

Mesh：

Substances：

Year: 2008 PMID： 18322011 PMCID： PMC2268770 DOI： 10.1073/pnas.0800935105

Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN： 0027-8424 Impact factor: 11.205

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21 in total

1. V(D)J recombinational accessibility-heading in the opposite direction?

Authors: Cosmas Giallourakis; Frederick W Alt; Craig H Bassing
Journal: Nat Immunol Date: 2004-06 Impact factor: 25.606

2. Antisense intergenic transcription in V(D)J recombination.

Authors: Daniel J Bolland; Andrew L Wood; Colette M Johnston; Sam F Bunting; Geoff Morgan; Lyubomira Chakalova; Peter J Fraser; Anne E Corcoran
Journal: Nat Immunol Date: 2004-04-25 Impact factor: 25.606

3. Both DNA strands of antibody genes are hypermutation targets.

Authors: C Milstein; M S Neuberger; R Staden
Journal: Proc Natl Acad Sci U S A Date: 1998-07-21 Impact factor: 11.205

4. Shutdown of class switch recombination by deletion of a switch region control element.

Authors: S Jung; K Rajewsky; A Radbruch
Journal: Science Date: 1993-02-12 Impact factor: 47.728

5. Two antisense promoters in the immunoglobulin mu-switch region drive expression of c-myc in the Burkitt's lymphoma cell line BL67.

Authors: T W Apel; J Mautner; A Polack; G W Bornkamm; D Eick
Journal: Oncogene Date: 1992-07 Impact factor: 9.867

6. Activation-induced cytidine deaminase (AID) can target both DNA strands when the DNA is supercoiled.

Authors: Hong Ming Shen; Ursula Storb
Journal: Proc Natl Acad Sci U S A Date: 2004-08-24 Impact factor: 11.205

7. Antisense transcripts from immunoglobulin heavy-chain locus V(D)J and switch regions.

Authors: Thomas Perlot; Gang Li; Frederick W Alt
Journal: Proc Natl Acad Sci U S A Date: 2008-02-21 Impact factor: 11.205

8. Separate domains of AID are required for somatic hypermutation and class-switch recombination.

Authors: Reiko Shinkura; Satomi Ito; Nasim A Begum; Hitoshi Nagaoka; Masamichi Muramatsu; Kazuo Kinoshita; Yoshimasa Sakakibara; Hiroko Hijikata; Tasuku Honjo
Journal: Nat Immunol Date: 2004-06-13 Impact factor: 25.606

9. Transcription enhances AID-mediated cytidine deamination by exposing single-stranded DNA on the nontemplate strand.

Authors: Almudena R Ramiro; Pete Stavropoulos; Mila Jankovic; Michel C Nussenzweig
Journal: Nat Immunol Date: 2003-05 Impact factor: 25.606

10. Translocated c-myc genes produce chimeric transcripts containing antisense sequences of the immunoglobulin heavy chain locus in mouse plasmacytomas.

Authors: M A Julius; A J Street; P D Fahrlander; J Q Yang; R N Eisenman; K B Marcu
Journal: Oncogene Date: 1988-05 Impact factor: 9.867

6 in total

Does antisense make sense of AID targeting?

1. V(D)J recombinational accessibility-heading in the opposite direction?

2. Antisense intergenic transcription in V(D)J recombination.

3. Both DNA strands of antibody genes are hypermutation targets.

4. Shutdown of class switch recombination by deletion of a switch region control element.

5. Two antisense promoters in the immunoglobulin mu-switch region drive expression of c-myc in the Burkitt's lymphoma cell line BL67.

6. Activation-induced cytidine deaminase (AID) can target both DNA strands when the DNA is supercoiled.

7. Antisense transcripts from immunoglobulin heavy-chain locus V(D)J and switch regions.

8. Separate domains of AID are required for somatic hypermutation and class-switch recombination.

9. Transcription enhances AID-mediated cytidine deamination by exposing single-stranded DNA on the nontemplate strand.

10. Translocated c-myc genes produce chimeric transcripts containing antisense sequences of the immunoglobulin heavy chain locus in mouse plasmacytomas.

1. Seeking sense of antisense switch transcripts.

2. Sense transcription through the S region is essential for immunoglobulin class switch recombination.

Review 3. Regulatory roles of natural antisense transcripts.

4. Determinants of R-loop formation at convergent bidirectionally transcribed trinucleotide repeats.

Review 5. Epigenomic Modifications Mediating Antibody Maturation.

6. Characterization of DNA G-Quadruplex Structures in Human Immunoglobulin Heavy Variable (IGHV) Genes.