LOCALIZED MRNA IN XENOPUS DEVELOPMENT
LOCALIZED MRNA IN XENOPUS DEVELOPMENT
批准号:
3467120
负责人:
DANIEL L. WEEKS
金额:
$9.03万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1988
资助国家:
美国
项目状态:
已结题
起止时间:
1988-07-01 至 1993-06-30
中文摘要
一个关于控制发展的长期理论
从受精卵到胚胎的过程是母体分子,
是受精前存在于卵子中的分子,
早期胚胎发生的事件。 通过母体定位
卵的特定区域,这些细胞是由
卵子的分裂会遗传不同的母体分子,
赋予他们独特的身份,
发展能力。 理解的职能作用
局部化的母体分子被认为是理解
控制早期发展。
有许多实验结果证实了
局部母体分子 最近有一类
已经鉴定了定位分子,信使RNA(mRNA
克隆。 这些最近的成功鼓励了对
定位mRNA作为理解
局部母体分子的作用。 实验系统
是一种叫做非洲爪蟾的青蛙。
在将要解决的问题中,
编码这些mRNA的基因的转录受到控制。
基因的主要序列将被检查,
相似性和差异性,以及假定的转录
将在卵母细胞发育过程中研究对照区,
胚胎发生,以发现影响它们的因素,
激活和抑制。 这些研究应该会带来更好的
了解是什么调节母体和胚胎
转录。
mRNA通过翻译成蛋白质发挥作用。 的
蛋白质的时间外观和胚胎定位
也将检测定位mRNA的产物。 这些
蛋白质将使用识别它们的抗体来可视化,
他们的功能研究都阐明了他们的相似之处,
通过结构分析已知功能的蛋白,
将其引入发育中的胚胎中以检查其影响
当错误定位,突变,或在更大的丰度比
通常存在于胚胎中。
最后,只有少数定位的mRNA被分离出来,
约会 这类母性的新成员的隔离
分子,来自卵子和胚胎的不同区域,
必要 这些新的分子将被识别和分离,
母体RNA衍生的cDNA λ的差异筛选
图书馆.
英文摘要
One long standing theory concerning the control of development
from fertilized egg into embryo is that maternal molecules, that
is molecules present in the egg prior to fertilization, direct the
events of early embryogenesis. By localization of maternal
molecules to specific regions of the egg, the cells that result from
cleavage of the egg inherit different sets of maternal molecules,
giving them a unique identity and endowing them with defined
developmental capacity. Understanding the functional role of
localized maternal molecules is viewed as a way to understand
control of early development.
There are many experimental results confirming the existence of
localized maternal molecules. Recently members of one class of
localized molecule, messenger RNA (mRNA) have been identified
and cloned. These recent successes encourages the study of
localized mRNA as a starting point towards understanding the
role of localized maternal molecules. The experimental system
that will be used is the frog, Xenopus laevis.
Among the questions that will be addressed, is the way the
transcription of the genes encoding these mRNA are controlled.
The primary sequence of the genes will be examined for
similarities and differences, and the putative transcriptional
control regions will be studied during oocyte development and
embryogenesis to discover the factor that influence both their
activation and repression. These studies should lead to a better
understanding of what regulates maternal and embryonic
transcription.
mRNA exert their role by being translated into proteins. The
temporal appearance, and embryonic localization of the protein
products of the localized mRNAs will also be examined. These
proteins will be visualized using antibodies that recognize them,
their functions studied both by elucidating their similarity to
proteins of known function by structural analysis, and by
introduction back into developing embryos to examine their affect
when mislocalized, mutated, or in greater abundance than
normally found in the embryo.
Finally, only a handful of localized mRNAs have been isolated to
date. The isolation of new members of this class of maternal
molecule, from different regions of the egg and embryo is
necessary. These new molecules will be identified and isolated by
differential screening of maternal RNA derived cDNA lambda
libraries.
期刊论文(4)
专著(0)
科研奖励(0)
会议论文
Cyclin B mRNA depletion only transiently inhibits the Xenopus embryonic cell cycle.
细胞周期蛋白 B mRNA 耗尽只会暂时抑制非洲爪蟾胚胎细胞周期。
DOI:
10.1242/dev.111.4.1173
发表时间:
1991
期刊:
Development (Cambridge, England)
影响因子:
--
作者:
[Weeks,DL, Walder,JA, Dagle,JM]
通讯作者:
Dagle,JM
Amyloids, aggregates and Nucleolar activity in Xenopus development
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批准号:10170380
-
项目类别:
-
资助金额:$30.4万
-
财政年份:2018
-
负责人:DANIEL L. WEEKS
-
依托单位:
Nkx2-5 and congenital heart defects in Xenopus
-
批准号:8469049
-
项目类别:
-
资助金额:$30.67万
-
财政年份:2004
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负责人:DANIEL L. WEEKS
-
依托单位:
Nkx2-5 and congenital heart defects in Xenopus
-
批准号:6992703
-
项目类别:
-
资助金额:$28.81万
-
财政年份:2004
-
负责人:DANIEL L. WEEKS
-
依托单位:
Nkx2-5 and congenital heart defects in Xenopus
-
批准号:6719707
-
项目类别:
-
资助金额:$29.5万
-
财政年份:2004
-
负责人:DANIEL L. WEEKS
-
依托单位:
Nkx2-5 and congenital heart defects in Xenopus
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批准号:7159309
-
项目类别:
-
资助金额:$27.97万
-
财政年份:2004
-
负责人:DANIEL L. WEEKS
-
依托单位:
Nkx2-5 and congenital heart defects in Xenopus
-
批准号:8269765
-
项目类别:
-
资助金额:$31.79万
-
财政年份:2004
-
负责人:DANIEL L. WEEKS
-
依托单位:
Nkx2-5 and congenital heart defects in Xenopus
-
批准号:6838792
-
项目类别:
-
资助金额:$29.5万
-
财政年份:2004
-
负责人:DANIEL L. WEEKS
-
依托单位:
Nkx2-5 and congenital heart defects in Xenopus
-
批准号:7987632
-
项目类别:
-
资助金额:$31.93万
-
财政年份:2004
-
负责人:DANIEL L. WEEKS
-
依托单位:
Nkx2-5 and congenital heart defects in Xenopus
-
批准号:8110014
-
项目类别:
-
资助金额:$31.79万
-
财政年份:2004
-
负责人:DANIEL L. WEEKS
-
依托单位:
CARDIOVASCULAR DEVELOPMENT IN XENOPUS LAEVIS
-
批准号:6565114
-
项目类别:
-
资助金额:$44.31万
-
财政年份:2002
-
负责人:DANIEL L. WEEKS
-
依托单位:
CARDIOVASCULAR DEVELOPMENT IN XENOPUS LAEVIS
-
批准号:6413002
-
项目类别:
-
资助金额:$44.31万
-
财政年份:2001
-
负责人:DANIEL L. WEEKS
-
依托单位:
CARDIOVASCULAR DEVELOPMENT IN XENOPUS LAEVIS
-
批准号:6302552
-
项目类别:
-
资助金额:$13.23万
-
财政年份:2000
-
负责人:DANIEL L. WEEKS
-
依托单位:
CARDIOVASCULAR DEVELOPMENT IN XENOPUS LAEVIS
-
批准号:6111046
-
项目类别:
-
资助金额:$13.23万
-
财政年份:1999
-
负责人:DANIEL L. WEEKS
-
依托单位:
CORE--MOLECULAR BIOLOGY
-
批准号:6109983
-
项目类别:
-
资助金额:$17.73万
-
财政年份:1998
-
负责人:DANIEL L. WEEKS
-
依托单位:
REGULATION OF ATRIOVENTRICULAR CANAL MESENCHYME FORMATION
-
批准号:6109980
-
项目类别:
-
资助金额:$17.73万
-
财政年份:1998
-
负责人:DANIEL L. WEEKS
-
依托单位:
TRIPLEX FORMING CATIONIC OLIGOS IN XENOPUS
-
批准号:2653326
-
项目类别:
-
资助金额:$10.0万
-
财政年份:1997
-
负责人:DANIEL L. WEEKS
-
依托单位:
REGULATION OF ATRIOVENTRICULAR CANAL MESENCHYME FORMATION
-
批准号:6242046
-
项目类别:
-
资助金额:$16.91万
-
财政年份:1997
-
负责人:DANIEL L. WEEKS
-
依托单位:
CORE--MOLECULAR BIOLOGY
-
批准号:6242049
-
项目类别:
-
资助金额:$16.91万
-
财政年份:1997
-
负责人:DANIEL L. WEEKS
-
依托单位:
LOCALIZED MRNA IN XENOPUS DEVELOPMENT
-
批准号:3467116
-
项目类别:
-
资助金额:$11.63万
-
财政年份:1988
-
负责人:DANIEL L. WEEKS
-
依托单位:
LOCALIZED MRNA IN XENOPUS DEVELOPMENT
-
批准号:3467117
-
项目类别:
-
资助金额:$7.97万
-
财政年份:1988
-
负责人:DANIEL L. WEEKS
-
依托单位:
海外基金