FUNCTION OF N-MYC PROTEIN IN LYMPHOCYTE DIFFERENTIATION
N-MYC 蛋白在淋巴细胞分化中的功能
基本信息
- 批准号:2443043
- 负责人:
- 金额:$ 15.65万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1993
- 资助国家:美国
- 起止时间:1993-07-01 至 1999-06-30
- 项目状态:已结题
- 来源:
- 关键词:B lymphocyte T lymphocyte apoptosis cell line cell nucleus chimeric proteins cytoplasm developmental genetics gene expression gene mutation gene targeting gestational age hematopoiesis hematopoietic growth factor immunofluorescence technique in situ hybridization laboratory mouse lymphocyte proliferation messenger RNA mutant nucleic acid probes nucleic acid sequence protooncogene temperature sensitive mutant tissue /cell culture transcription factor
项目摘要
N-myc is a member of a family of proto-oncogenes that encode related but
distinct nuclear proteins. Myc genes are putative transcription factors
that are thought to function in the regulation of gene expression in the
context of cell growth and differentiation. However, the exact function
of myc genes is unknown. Each myc gene is associated with a unique
tissue-specific pattern of spontaneously arising tumors that partially
reflects the expression pattern in normal development. The finding that
a null mutation of N-myc when homozygous in the germline of the mouse is
embryonic lethal suggests that N-myc plays a unique physiological role
during development.
N-myc is highly regulated during B lymphocyte development. Pre-B cells
express both c-myc and N-myc. The expression of c-myc and N-myc mRNA is
induced in normal pre-B cells by treatment with the pre-B cell specific
growth factor IL-7; at this stage, regulation is mediated by releasing a
block to transcriptional elongation. When cells mature to the B cell
stage, transcriptional initiation of N-myc is down-regulated, while c-myc
continues to be expressed. Together, these findings suggest that N-myc
has a specific function in the early stages of B cell development. We
hypothesize that N-myc is required for the expansion of precursor B cells
either by promoting their growth, inhibiting their death, and/or
preventing their terminal differentiation. The goal of these studies is
to define precisely the function of N-myc during B lymphocyte development
and how it relates to c-myc function. How N-myc may be involved in
determination of other hematopoietic lineages will also be examined.
The exact stages within B lymphocyte and T lymphocyte differentiation
when N-myc is expressed will be determined. This expression will be
correlated with expression of other stage-specific features within that
lineage. The affect of a null N-myc mutation on development of committed
and uncommitted progenitor cells will be determined. If a maturational
block in B cell development is found, the differentiation stage at which
it occurs will be defined and characterized. Transformed and
nontransformed cell lines will be derived in order to determine how
expression of other stage-specific genes are affected by lack of N-myc
expression. The response of these cells to growth factor and mitogenic
signals will be tested. A novel approach is presented for the derivation
of immortalized cell lines that represent B cell differentiation stages
and that retain full differentiative capacity is presented. Using "hit
and run" gene targeting techniques, the sequences within each of the myc
genes that determine their unique functions within lymphocyte
differentiation will be determined. Finally, we will determine if N-myc
may function during hematopoiesis by induction of apoptosis or modulation
of c-myc-induced apoptosis.
Besides providing insights into the molecular mechanisms underlying
lymphocyte development, these studies may also yield revelations about
myc gene function generally during embryogenesis and how transcription
factors function in developmental processes. Furthermore, an
understanding of how myc genes function in normal development may reveal
how inappropriate expression leads to oncogenesis.
N-myc是原癌基因家族的成员,编码相关的但是
项目成果
期刊论文数量(3)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Truncated immunoglobulin Dmu causes incomplete developmental progression of RAG-deficient pro-B cells.
截短的免疫球蛋白 Dmu 会导致 RAG 缺陷的亲 B 细胞发育不完全。
- DOI:10.1016/s0161-5890(01)00085-2
- 发表时间:2002
- 期刊:
- 影响因子:3.6
- 作者:Malynn,BarbaraA;Shaw,AlbertC;Young,Faith;Stewart,Valerie;Alt,FrederickW
- 通讯作者:Alt,FrederickW
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BARBARA A MALYNN其他文献
BARBARA A MALYNN的其他文献
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{{ truncateString('BARBARA A MALYNN', 18)}}的其他基金
FUNCTION OF N-MYC PROTEIN IN LYMPHOCYTE DIFFERENTIATION
N-MYC 蛋白在淋巴细胞分化中的功能
- 批准号:
2101775 - 财政年份:1993
- 资助金额:
$ 15.65万 - 项目类别:
FUNCTION OF N-MYC PROTEIN IN LYMPHOCYTE DIFFERENTIATION
N-MYC 蛋白在淋巴细胞分化中的功能
- 批准号:
3460858 - 财政年份:1993
- 资助金额:
$ 15.65万 - 项目类别:
FUNCTION OF N-MYC PROTEIN IN LYMPHOCYTE DIFFERENTIATION
N-MYC 蛋白在淋巴细胞分化中的功能
- 批准号:
2101774 - 财政年份:1993
- 资助金额:
$ 15.65万 - 项目类别:
FUNCTION OF N-MYC PROTEIN IN LYMPHOCYTE DIFFERENTIATION
N-MYC 蛋白在淋巴细胞分化中的功能
- 批准号:
2101776 - 财政年份:1993
- 资助金额:
$ 15.65万 - 项目类别:
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