DEPDC1 is a novel cell cycle related gene that regulates mitotic progression
被引:39
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作者:
Mi, Yan
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Chongqing Med Univ, Affiliated Hosp 1, Dept Otolaryngol, Chongqing 400016, Peoples R ChinaChongqing Med Univ, Affiliated Hosp 1, Dept Otolaryngol, Chongqing 400016, Peoples R China
Mi, Yan
[1
]
Zhang, Chundong
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机构:
Chongqing Med Univ, Dept Biochem & Mol Biol, Chongqing 400016, Peoples R China
Chongqing Med Univ, Mol Med & Canc Res Ctr, Chongqing 400016, Peoples R ChinaChongqing Med Univ, Affiliated Hosp 1, Dept Otolaryngol, Chongqing 400016, Peoples R China
Zhang, Chundong
[2
,3
]
Bu, Youquan
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机构:
Chongqing Med Univ, Dept Biochem & Mol Biol, Chongqing 400016, Peoples R China
Chongqing Med Univ, Mol Med & Canc Res Ctr, Chongqing 400016, Peoples R ChinaChongqing Med Univ, Affiliated Hosp 1, Dept Otolaryngol, Chongqing 400016, Peoples R China
Bu, Youquan
[2
,3
]
Zhang, Ying
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Chongqing Med Univ, Dept Biochem & Mol Biol, Chongqing 400016, Peoples R China
Chongqing Med Univ, Mol Med & Canc Res Ctr, Chongqing 400016, Peoples R ChinaChongqing Med Univ, Affiliated Hosp 1, Dept Otolaryngol, Chongqing 400016, Peoples R China
Zhang, Ying
[2
,3
]
He, Longxia
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Chongqing Med Univ, Affiliated Hosp 1, Dept Otolaryngol, Chongqing 400016, Peoples R China
Chongqing Med Univ, Mol Med & Canc Res Ctr, Chongqing 400016, Peoples R ChinaChongqing Med Univ, Affiliated Hosp 1, Dept Otolaryngol, Chongqing 400016, Peoples R China
He, Longxia
[1
,3
]
Li, Hongxia
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Chongqing Med Univ, Affiliated Hosp 1, Dept Otolaryngol, Chongqing 400016, Peoples R China
Chongqing Med Univ, Mol Med & Canc Res Ctr, Chongqing 400016, Peoples R ChinaChongqing Med Univ, Affiliated Hosp 1, Dept Otolaryngol, Chongqing 400016, Peoples R China
Li, Hongxia
[1
,3
]
Zhu, Huifang
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Chongqing Med Univ, Dept Biochem & Mol Biol, Chongqing 400016, Peoples R China
Chongqing Med Univ, Mol Med & Canc Res Ctr, Chongqing 400016, Peoples R ChinaChongqing Med Univ, Affiliated Hosp 1, Dept Otolaryngol, Chongqing 400016, Peoples R China
Zhu, Huifang
[2
,3
]
Li, Yi
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Chongqing Med Univ, Dept Biochem & Mol Biol, Chongqing 400016, Peoples R China
Chongqing Med Univ, Mol Med & Canc Res Ctr, Chongqing 400016, Peoples R ChinaChongqing Med Univ, Affiliated Hosp 1, Dept Otolaryngol, Chongqing 400016, Peoples R China
Li, Yi
[2
,3
]
Lei, Yunlong
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Chongqing Med Univ, Dept Biochem & Mol Biol, Chongqing 400016, Peoples R China
Chongqing Med Univ, Mol Med & Canc Res Ctr, Chongqing 400016, Peoples R ChinaChongqing Med Univ, Affiliated Hosp 1, Dept Otolaryngol, Chongqing 400016, Peoples R China
Lei, Yunlong
[2
,3
]
Zhu, Jiang
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Chongqing Med Univ, Affiliated Hosp 1, Dept Otolaryngol, Chongqing 400016, Peoples R ChinaChongqing Med Univ, Affiliated Hosp 1, Dept Otolaryngol, Chongqing 400016, Peoples R China
Zhu, Jiang
[1
]
机构:
[1] Chongqing Med Univ, Affiliated Hosp 1, Dept Otolaryngol, Chongqing 400016, Peoples R China
[2] Chongqing Med Univ, Dept Biochem & Mol Biol, Chongqing 400016, Peoples R China
[3] Chongqing Med Univ, Mol Med & Canc Res Ctr, Chongqing 400016, Peoples R China
DEPDC1 is a recently identified novel tumor-related gene that is upregulated in several types of cancer and contributes to tumorigenesis. In this study, we have investigated the expression pattern and functional implications of DEPDC1 during cell cycle progression. Expression studies using synchronized cells demonstrated that DEPDC1 is highly expressed in the mitotic phase of the cell cycle. Immunofluorescence assays showed that DEPDC1 is predominantly localized in the nucleus during interphase and is redistributed into the whole cell upon nuclear membrane breakdown in metaphase. Subsequently, siRNA-mediated knockdown of DEPDC1 caused a significant mitotic arrest. Moreover, knockdown of DEPDC1 resulted in remarkable mitotic defects such as abnormal multiple nuclei and multipolar spindle structures accompanied by the upregulation of the A20 gene as well as several cell cycle-related genes such as CCNB1 and CCNB2. Taken together, our current observations strongly suggest that this novel cancerous gene, DEPDC1, plays a pivotal role in the regulation of proper mitotic progression.
机构:
Nagoya City Univ, Grad Sch Med Sci, Dept Biochem & Cell Biol, Mizuho Ku, Nagoya, Aichi 4678601, JapanNagoya City Univ, Grad Sch Med Sci, Dept Biochem & Cell Biol, Mizuho Ku, Nagoya, Aichi 4678601, Japan
Zineldeen, Doaa H.
Shimada, Midori
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机构:
Nagoya City Univ, Grad Sch Med Sci, Dept Biochem & Cell Biol, Mizuho Ku, Nagoya, Aichi 4678601, JapanNagoya City Univ, Grad Sch Med Sci, Dept Biochem & Cell Biol, Mizuho Ku, Nagoya, Aichi 4678601, Japan
Shimada, Midori
Niida, Hiroyuki
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Nagoya City Univ, Grad Sch Med Sci, Dept Biochem & Cell Biol, Mizuho Ku, Nagoya, Aichi 4678601, JapanNagoya City Univ, Grad Sch Med Sci, Dept Biochem & Cell Biol, Mizuho Ku, Nagoya, Aichi 4678601, Japan
Niida, Hiroyuki
Katsuno, Yuko
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Nagoya City Univ, Grad Sch Med Sci, Dept Biochem & Cell Biol, Mizuho Ku, Nagoya, Aichi 4678601, JapanNagoya City Univ, Grad Sch Med Sci, Dept Biochem & Cell Biol, Mizuho Ku, Nagoya, Aichi 4678601, Japan
Katsuno, Yuko
Nakanishi, Makoto
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Nagoya City Univ, Grad Sch Med Sci, Dept Biochem & Cell Biol, Mizuho Ku, Nagoya, Aichi 4678601, JapanNagoya City Univ, Grad Sch Med Sci, Dept Biochem & Cell Biol, Mizuho Ku, Nagoya, Aichi 4678601, Japan