기관회원 [로그인]
소속기관에서 받은 아이디, 비밀번호를 입력해 주세요.
개인회원 [로그인]

비회원 구매시 입력하신 핸드폰번호를 입력해 주세요.
본인 인증 후 구매내역을 확인하실 수 있습니다.

회원가입
서지반출
Coordinated Spatial and Temporal Expression of Voltage-sensitive calcium Channel ${alpha}_{1A}$ and $eta_4$ Subunit mRNAs in Rat Cerebellum
[STEP1]서지반출 형식 선택
파일형식
@
서지도구
SNS
기타
[STEP2]서지반출 정보 선택
  • 제목
  • URL
돌아가기
확인
취소
  • Coordinated Spatial and Temporal Expression of Voltage-sensitive calcium Channel ${alpha}_{1A}$ and $eta_4$ Subunit mRNAs in Rat Cerebellum
  • Coordinated Spatial and Temporal Expression of Voltage-sensitive calcium Channel ${alpha}_{1A}$ and $eta_4$ Subunit mRNAs in Rat Cerebellum
저자명
Kim. Dong-Sun-Chin. Hemin,Chin. Hemin-Chin
간행물명
Korean journal of biological sciences
권/호정보
1997년|1권 4호|pp.589-594 (6 pages)
발행정보
한국동물학회
파일정보
정기간행물|ENG|
PDF텍스트
주제분야
기타
이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
서지반출

기타언어초록

The neuronal voltage-sensitive calcium channels (VSCCs) are multisubunit complexes consisting of $alpha_1,;alpha_2-delta$ and $eta$ subunits. Heterologous expression and biochemical studies have shown that the activity of VSCCs is regulated by their $eta$ subunits in a $eta$ subunit isoform-specific manner. To elucidate the $eta$ subunit identity of the P/Q-type calcium channel encoded by an $alpha_{1A}$ subunit, which is exclusively expressed in the Purkinje and granule cell of the cerebellum, we have examined the spatial and temporal expression patterns of $eta$ subunits and compared them with those of $alpha_{1A}$ subunit in the developing rat cerebellum. Reverse transcriptase- polymerase chain reaction (RT-PCR) and Northern blot analysis have shown that $eta_4$ subunit mRNA was prominently expressed in the cerebellum and much more abundant than any other distinct $eta$ subunits. RNase protection assay has further demonstrated that the expression of $alpha_{1A}$ and $eta_4$ subunits increased during cerebellar development, while the amount of $eta_2$ and $eta_3$ mRNAs did not significantly change. In addition, a $eta_4$ transcript was present in cultured cerebellar granule cells, but not in astrocyte cells, and the level of $eta_4$ mRNA expression increased gradually in vitro seen as in vivo. Based on the spatial and temporal expression patterns of $eta_4$ subunit, we conclude that $eta_4$ may predominantly associate, but probably not exclusively, with the $alpha_{1A}$ subunit in rat cerebellar granule cells.