4.5 Article

ANRIL is implicated in the regulation of nucleus and potential transcriptional target of E2F1

Journal

ONCOLOGY REPORTS
Volume 24, Issue 3, Pages 701-707

Publisher

SPANDIDOS PUBL LTD
DOI: 10.3892/or_00000910

Keywords

ANRIL; CDKN2A; E2F1; nucleus; non-coding RNA

Categories

Funding

  1. Institute of Science and Technology Meiji University
  2. Tokai University Educational System General Research Organization
  3. Grants-in-Aid for Scientific Research [22241049] Funding Source: KAKEN

Ask authors/readers for more resources

ANRIL, a large antisense non-coding RNA, is in the proximity of CDKN2A and overlapped with CDKN2B at human chromosome 9p21, and has been strongly implicated in the association with high risk genetic markers of coronary artery disease (CAD). Mice model harboring large deletion of posterior part of ANRIL and CAD high risk genetic markers resulted in substantial suppression of both CDKN2A and CDKN2B; however, the mechanistic insights of regulation and function of ANRIL have remain elusive. To date multiple splice variants of ANRIL have been reported and expression of specific splice variant of ANRIL has been shown to be tightly associated with 9p21 CAD high risk markers. Here we identified a new splice variant of ANRIL and introduced it into HeLa cells to uncover functional aspects of ANRIL towards cellular function. For this purpose, we monitored global mRNA expressional changes and conducted gene ontology enrichment. The majority of mRNAs was down-regulated by ANRIL overexpression. Among them, a subset of mRNAs particularly involved in the regulation of nucleus and establishment or maintenance of chromatin architecture was significantly enriched. Such a circumstance was manifested after 48 h of ANRIL overexpression but no significant changes were seen after 24 h of ANRIL overexpression. Next we analyzed the sequences containing the intergenic region between ANRIL and CDKN2A (p14ARF) by introducing the sequences upstream of luciferase reporter gene. Based on the luciferase activity, the sequences tested were shown to act as promoter for ANRIL and p14ARF. Moreover, as well p14ARF, ANRIL promoter was responsive to transcription factor E2F1 in HeLa and A549 cells. Taken together, our present results indicate that co-regulation of ANRIL and p14ARF could be coupled by their unique intergenic region potentially through E2F1. Judged from the suppressive effect of ANRIL on a subset of mRNAs involved in the nuclear function suggests that ANRIL might have silencing effect on a specific gene set that accounts for a wide array of gene expression.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Nutrition & Dietetics

Association between Vitamin Intake and Chronic Kidney Disease According to a Variant Located Upstream of the PTGS1 Gene: A Cross-Sectional Analysis of Shika Study

Kim-Oanh Pham, Akinori Hara, Hiromasa Tsujiguchi, Keita Suzuki, Fumihiko Suzuki, Sakae Miyagi, Takayuki Kannon, Takehiro Sato, Kazuyoshi Hosomichi, Hirohito Tsuboi, Thao Thi Thu Nguyen, Yukari Shimizu, Yasuhiro Kambayashi, Masaharu Nakamura, Chie Takazawa, Haruki Nakamura, Toshio Hamagishi, Aki Shibata, Tadashi Konoshita, Atsushi Tajima, Hiroyuki Nakamura

Summary: This study aimed to investigate the interaction between dietary vitamin intake and the rs883484 genotype in the development of CKD. The results showed that higher intake of niacin, alpha-tocopherol, and vitamin C were independently associated with a lower tendency of CKD in individuals with the minor homozygotes of the rs883484 gene variant. This suggests the importance of dietary vitamin intake in preventing CKD in middle-aged to older-aged Japanese individuals with this specific gene variant.

NUTRIENTS (2022)

Article Clinical Neurology

Association Between Serum 25-Hydroxyvitamin D Concentrations, CDX2 Polymorphism in Promoter Region of Vitamin D Receptor Gene and Chronic Pain in Rural Japanese Residents

Keita Suzuki, Hiromasa Tsujiguchi, Akinori Hara, Oanh Kim Pham, Sakae Miyagi, Thao Thi Thu Nguyen, Haruki Nakamura, Fumihiko Suzuki, Tomoko Kasahara, Yukari Shimizu, Yohei Yamada, Yasuhiro Kambayashi, Hirohito Tsuboi, Takehiro Sato, Takayuki Kannon, Kazuyoshi Hosomichi, Atsushi Tajima, Toshinari Takamura, Hiroyuki Nakamura

Summary: This study investigated the association between chronic pain, serum 25-hydroxyvitamin D concentrations, and single nucleotide polymorphisms. The results suggest that lower serum 25-hydroxyvitamin D concentrations are associated with chronic pain in individuals with a specific polymorphism.

JOURNAL OF PAIN RESEARCH (2022)

Article Multidisciplinary Sciences

Localized astrogenesis regulates gyrification of the cerebral cortex

Yohei Shinmyo, Kengo Saito, Toshihide Hamabe-Horiike, Narufumi Kameya, Akitaka Ando, Kanji Kawasaki, Tung Anh Dinh Duong, Masataka Sakashita, Jureepon Roboon, Tsuyoshi Hattori, Takayuki Kannon, Kazuyoshi Hosomichi, Michal Slezak, Matthew G. Holt, Atsushi Tajima, Osamu Hori, Hiroshi Kawasaki

Summary: This study reveals the important role of localized astrogenesis in gyrus formation in the mammalian brain. The findings suggest that the positive feedback loop of FGF signaling is a crucial mechanism underlying cortical folding.

SCIENCE ADVANCES (2022)

Article Genetics & Heredity

Genetic factors associated with serum amylase in a Japanese population: combined analysis of copy-number and single-nucleotide variants

Zannatun Nayema, Takehiro Sato, Takayuki Kannon, Hiromasa Tsujiguchi, Kazuyoshi Hosomichi, Hiroyuki Nakamura, Atsushi Tajima

Summary: Amylase activity and levels are heritable quantitative traits. A genome-wide association study (GWAS) in 814 Japanese individuals identified significant single-nucleotide variants (SNVs) near the AMY cluster on chromosome 1 that are associated with serum amylase levels (SAL). The study also found that the diploid copy number of AMY1 is significantly associated with SAL, while no significant associations were found for AMY2A or AMY2B. The AMY1 CNV appears to be the major genetic factor influencing SAL in the Japanese population.

JOURNAL OF HUMAN GENETICS (2023)

Article Psychology, Multidisciplinary

Relationships among Depressive Symptoms, Body Weight, and Chronic Pain: A Cross-Sectional Analysis of the Shika Study

Shinobu Fukushima, Fumihiko Suzuki, Hiromasa Tsujiguchi, Akinori Hara, Sakae Miyagi, Takayuki Kannon, Keita Suzuki, Yukari Shimizu, Thao Thi Thu Nguyen, Toru Yanagisawa, Fumika Oku, Kuniko Sato, Masaharu Nakamura, Koichiro Hayashi, Aki Shibata, Tadashi Konoshita, Yasuhiro Kambayashi, Hirohito Tsuboi, Atsushi Tajima, Hiroyuki Nakamura

Summary: This study investigated the relationships among depression, body mass index (BMI), and chronic pain (CP). The results showed a positive correlation between depression and lumbar/knee pain in the BMI < 25 group, but not in the BMI >= 25 group. Additionally, a higher BMI was associated with lumbar/knee pain.

BEHAVIORAL SCIENCES (2023)

Article Cardiac & Cardiovascular Systems

The utility of zebrafish cardiac arrhythmia model to predict the pathogenicity of KCNQ1 variants

Shihe Cui, Kenshi Hayashi, Isao Kobayashi, Kazuyoshi Hosomichi, Akihiro Nomura, Ryota Teramoto, Keisuke Usuda, Hirofumi Okada, Yaowen Deng, Jingjing Kobayashi-Sun, Tetsuo Nishikawa, Hiroshi Furusho, Takekatsu Saito, Hiroaki Hirase, Kunio Ohta, Manabu Fujimoto, Yuki Horita, Takashi Kusayama, Toyonobu Tsuda, Hayato Tada, Takeshi Kato, Soichiro Usui, Kenji Sakata, Noboru Fujino, Atsushi Tajima, Masakazu Yamagishi, Masayuki Takamura

Summary: Genetic testing is crucial for identifying disease-causing variants and distinguishing between pathogenic and benign variants. In this study, a zebrafish model was used to investigate the clinical significance of KCNQ1 variants. The results showed that KCNQ1 variants could affect action potential duration and should be reevaluated physiologically.

JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (2023)

Article Nutrition & Dietetics

Higher Intake of Vegetable Protein and Lower Intake of Animal Fats Reduce the Incidence of Diabetes in Non-Drinking Males: A Prospective Epidemiological Analysis of the Shika Study

Aya Ogawa, Hiromasa Tsujiguchi, Masaharu Nakamura, Koichi Hayashi, Akinori Hara, Keita Suzuki, Sakae Miyagi, Takayuki Kannon, Chie Takazawa, Jiaye Zhao, Yasuhiro Kambayashi, Yukari Shimizu, Aki Shibata, Tadashi Konoshita, Fumihiko Suzuki, Hirohito Tsuboi, Atsushi Tajima, Hiroyuki Nakamura

Summary: This study investigated the interrelationships among nutrient intake, alcohol consumption, and the incidence of diabetes. It found that vegetable protein intake was negatively associated with the incidence of diabetes in males, while animal fat intake was positively associated with the incidence of diabetes. Therefore, considering vegetable protein and animal fat intake, along with drinking habits, is important for the prevention of diabetes.

NUTRIENTS (2023)

Article Nutrition & Dietetics

Nutrigenetic Interaction Between Apolipoprotein C3 Polymorphism and Fat Intake in People with Nonalcoholic Fatty Liver Disease

Reina Yamamoto, Yumie Takeshita, Hiromasa Tsujiguchi, Takayuki Kannon, Takehiro Sato, Kazuyoshi Hosomichi, Keita Suzuki, Yuki Kita, Takeo Tanaka, Hisanori Goto, Yujiro Nakano, Tatsuya Yamashita, Shuichi Kaneko, Atsushi Tajima, Hiroyuki Nakamura, Toshinari Takamura

Summary: Recent studies have shown that nonalcoholic fatty liver disease (NAFLD) is correlated with genetic polymorphisms. However, the effects of genetic variation on nutritional metabolism and NAFLD are complex and further studies are needed.

CURRENT DEVELOPMENTS IN NUTRITION (2023)

Article Biochemistry & Molecular Biology

Postnatal expression of CD38 in astrocytes regulates synapse formation and adult social memory

Tsuyoshi Hattori, Stanislav M. Cherepanov, Ryo Sakaga, Jureepon Roboon, Dinh Thi Nguyen, Hiroshi Ishii, Mika Takarada-Iemata, Takumi Nishiuchi, Takayuki Kannon, Kazuyoshi Hosomichi, Atsushi Tajima, Yasuhiko Yamamoto, Hiroshi Okamoto, Akira Sugawara, Haruhiro Higashida, Osamu Hori

Summary: This study reveals that astrocytes, specifically the CD38 protein expressed in them, play a crucial role in social behavior by regulating oxytocin release and synapse formation. Deletion of CD38 in postnatal astrocytes impairs social memory and inhibits synaptogenesis, highlighting the importance of astrocytes in neural circuit formation.

EMBO JOURNAL (2023)

Article Nutrition & Dietetics

Distinct associations between dietary omega-3 and omega-6 fatty acids intake with chronic kidney disease in adults with and without diabetes: A cross-sectional study

Akinori Hara, Hiromasa Tsujiguchi, Keita Suzuki, Masaharu Nakamura, Masaru Okada, Jiaye Zhao, Chie Takazawa, Fumihiko Suzuki, Tomoko Kasahara, Yukari Shimizu, Hirohito Tsuboi, Takayuki Kannon, Atsushi Tajima, Toshinari Takamura, Hiroyuki Nakamura

Summary: The study explored the relationship between dietary intake of fatty acids and chronic kidney disease (CKD) in Japanese people. It found that low intake of omega-3 and high omega-6-to-omega-3 ratio were associated with CKD in participants with diabetes, but not in those without diabetes.

NUTRITION (2023)

Article Multidisciplinary Sciences

A comprehensive risk factor analysis using association rules in people with diabetic kidney disease

Tadashi Toyama, Miho Shimizu, Taihei Yamaguchi, Hidekazu Kurita, Tetsurou Morita, Megumi Oshima, Shinji Kitajima, Akinori Hara, Norihiko Sakai, Atsushi Hashiba, Takuzo Takayama, Atsushi Tajima, Kengo Furuichi, Takashi Wada, Yasunori Iwata

Summary: Association rule, a transparent machine learning method, was used to evaluate the risk for kidney disease in diabetic patients. The study found significant relationships between glycemic control, anemia, obesity, and hypertension with kidney function. Stratified risk assessment using association rules revealed the importance of the presence or absence of risk factors.

SCIENTIFIC REPORTS (2023)

Article Chemistry, Multidisciplinary

An Observational Study on Changes in the Oral and Gut Microbiota through Professional Mechanical Tooth Cleaning, including Tooth-Brushing Instructions in Patients with Multi-Bracket Appliances

Satoko Okuwaki, Kazuyoshi Hosomichi, Atsushi Tajima, Tetsutaro Yamaguchi

Summary: In this study, continuous professional mechanical tooth cleaning (PMTC) for orthodontic patients wearing multi-bracket appliances was found to significantly reduce plaque in the oral cavity without causing changes in the oral or gut microbiota or an increase in pathogenic bacteria. This suggests that continuous PMTC can inhibit the growth of pathogenic bacteria by maintaining a clean oral environment and avoiding dysbiosis in both the oral and gut microbiota. Furthermore, differences in food intake and choices at each treatment stage may affect the gut microbiota.

APPLIED SCIENCES-BASEL (2023)

Article Health Care Sciences & Services

Association between Bone Mineral Density and Oral Frailty on Renal Function: Findings from the Shika Study

Shingo Nakai, Fumihiko Suzuki, Shigefumi Okamoto, Sakae Miyagi, Hiromasa Tsujiguchi, Akinori Hara, Thao Thi Thu Nguyen, Yukari Shimizu, Koichiro Hayashi, Keita Suzuki, Tomoko Kasahara, Masaharu Nakamura, Chie Takazawa, Takayuki Kannon, Atsushi Tajima, Hirohito Tsuboi, Noriyoshi Ogino, Tadashi Konoshita, Toshinari Takamura, Hiroyuki Nakamura

Summary: This study aimed to investigate the association between oral frailty and decreased bone mineral density (BMD) and renal function. The results showed that lower BMD was significantly associated with lower renal function in individuals with an estimated glomerular filtration rate (eGFR) of < 60 and oral frailty. Further longitudinal studies are needed to confirm these findings.

HEALTHCARE (2023)

Article Genetics & Heredity

Identification of potential disease-associated variants in idiopathic generalized epilepsy using targeted sequencing

Regina Gamirova, Elena Shagimardanova, Takehiro Sato, Takayuki Kannon, Rimma Gamirova, Atsushi Tajima

Summary: This study aimed to explore the genetics of idiopathic generalized epilepsy (IGE) and identify candidate gene variants associated with IGE. Through whole-exome sequencing analysis, the study found that IGE shows high heterogeneity and identified several novel candidate variants. The results suggest that the current Genes4Epilepsy panel is incomplete for the clinical diagnosis of IGE.

JOURNAL OF HUMAN GENETICS (2023)

Letter Oncology

Minor GPI(-) granulocyte populations in aplastic anemia and healthy individuals derived from a few PIGA-mutated hematopoietic stem progenitor cells

Hiroki Mizumaki, Dung Cao Tran, Kohei Hosokawa, Kazuyoshi Hosomichi, Yoshitaka Zaimoku, Hiroyuki Takamatsu, Hirohito Yamazaki, Ken Ishiyama, Rena Yamazaki, Hiroshi Fujiwara, Atsushi Tajima, Shinji Nakao

BLOOD CANCER JOURNAL (2023)

No Data Available