2013
DOI: 10.5483/bmbrep.2013.46.3.171
|View full text |Cite
|
Sign up to set email alerts
|

Identification of a novel circularized transcript of the AML1 gene

Abstract: The AML1 gene is an essential transcription factor regulating the differentiation of hematopoietic stem cells into mature blood cells. Though at least 12 different alternatively spliced AML1 mRNAs are generated, three splice variants (AML1a, AML1b and AML1c) have been characterized. Here, using the reverse transcription-polymerase chain reaction with outwardfacing primers, we identified a novel non-polyadenylated transcript from the AML1 gene, with exons 5 and 6 scrambled. The novel transcript resisted RNase R… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
4
0

Year Published

2014
2014
2022
2022

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(4 citation statements)
references
References 22 publications
0
4
0
Order By: Relevance
“…Following the observation of circular molecules in viral genome, the first circRNAs in eukaryotic cells were confirmed in the cytoplasmic region of HeLa cells [4], and yeast mitochondrial RNA [5]. Subsequent evidence on individual circRNAs was then continually reported in different human and rat tissues, for example circRNAs derived from ETS-1, SRY, P450, ABP, DYSTROPHIN, MBL, and AML [6][7][8][9][10][11][12]. Though multiple experiments prove the existence of circRNAs, the identified circRNAs were generally less abundant than the linear products from the same parental genes.…”
Section: Background: Origin Of Circrnas As Functional Noncoding Rnasmentioning
confidence: 99%
“…Following the observation of circular molecules in viral genome, the first circRNAs in eukaryotic cells were confirmed in the cytoplasmic region of HeLa cells [4], and yeast mitochondrial RNA [5]. Subsequent evidence on individual circRNAs was then continually reported in different human and rat tissues, for example circRNAs derived from ETS-1, SRY, P450, ABP, DYSTROPHIN, MBL, and AML [6][7][8][9][10][11][12]. Though multiple experiments prove the existence of circRNAs, the identified circRNAs were generally less abundant than the linear products from the same parental genes.…”
Section: Background: Origin Of Circrnas As Functional Noncoding Rnasmentioning
confidence: 99%
“…To evaluate cytokine mRNA expression levels, RAW264.7 cells pre-treated with MPP (0~50 µM) for 30 min were incubated with LPS (1 µg/ml) for 6 h. Total RNA was isolated using TRIzol Reagent (Gibco BRL) according to the manufacturer's instructions, and stored at –70℃ until further use. Semiquantitative RT reactions were conducted as previously reported [ 19 ]. The primers (Bioneer, Seoul, Korea) used in these experiments are listed in Table 1 (F: forward, R: reverse).…”
Section: Methodsmentioning
confidence: 99%
“…To evaluate cytokine mRNA expression levels, RAW264.7 cells pre-treated with Gl-ME (0-300 μg/mL) for 30 min were incubated with LPS (1 μg/mL) for 6 h. Total RNA was isolated using TRIzol Reagent (Gibco BRL) according to the manufacturer's instructions and stored at À70°C until further use. Semiquantitative RT reactions were conducted as previously reported (Xu et al, 2013). The primers (Bioneer, Seoul, Korea) used in these experiments are listed in Table 1 (F: forward, R: reverse).…”
Section: Methodsmentioning
confidence: 99%