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Engineering Research

Location:
United States
Posted:
August 06, 2014

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Resume:

CURRICULUM VITAE

Name: Yunlong He, Ph.D.

Email: ****@****.***.***

Work phone #: 301-***-****

Education:

**** *.*. (Biotechnology), Shandong University, Jinan, Shandong, China

**** **.*. (Molecular Microbiology), Shanghai Jiao Tong University, Shanghai, China

Brief Research Experience:

July, 2010-present: Visiting Fellow in Laboratory of Cancer Biology and Genetics, Center for

Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD

1. I generated a transcriptional factor (Tcf1) conditional knockout mouse Tcf1flox/flox. The

master regulator Tcf1 can be deleted in specific tissues or development stages. When

crossed with β-actin cre mice, the homozygous mice Tcf1-/- are partially embryonic

lethal (70% less than Mendel ratio). We did RNA-Seq in Tcf1flox/flox and Tcf1-/-

embryonic stem cells and found Tcf1 is a master regulator for fatty acid metabolism.

It’s also relevant to clear cell renal cell carcinoma (CCRCC). (ongoing work)

The lineage control role of p53 in bone marrow-derived mesenchymal stem cells

2.

(MSCs) and its relevance to osteosarcoma-genesis. My study found p53 inhibits

osteogenic differentiation of MSCs by repressing RunX2, a master regulator of

osteogenesis, but doesn’t affect adipogenic and chondrogenic differentiation. And the

repression was indirectly through miR34s. It indicates that p53 activity can influence

cell fate decision in MSCs, and provide molecular and cellular insight into the

observation that p53 loss is associated with increased osteosarcoma incidence.

(preparing for submission, 2014, first author)

3. To identify p53 targets in a global and unbiased manner, we performed gene expression

microarray and ChIP-chip assays using mouse embryonic fibroblasts (MEFs) and mouse

embryonic stem (mES) cells. We found a novel p53 downstream target, Rap2b which

promotes cell survival after DNA damage. (Cell Cycle, 2013, co-first author)

Yunlong He – CV and Bibliography

4. Whole-genome study of p53-mediated DNA damage signaling in mES cells reveal that

binding of p53 at the promoter region significantly correlates with gene activation but not

with repression. Unexpectedly, we identify a regulatory mode for p53-mediated repression

through interfering with distal enhancer activity. Importantly, many ES cell-enriched core

transcription factors are p53-repressed genes. (Mol Cell, 2012, second author)

2002-2010: Graduate student in Microbial Metabolism Laboratory at Shanghai Jiao Tong

University, Shanghai, China (Supervisor: Prof. Zixin Deng)

Cloning type I polyketide synthase (PKS) gene clusters of meilingmycin from Streptomyces

1.

nanchangensis. Our work provides a more specific strategy for the cloning of modular type

I PKS gene clusters by use of acyltransferase-ketoreductase didomain PCR amplification.

The cloning of the meilingmycin gene clusters paves the way for its pathway engineering.

(Appl Environ Microbiol, 2010, first author)

I constructed two efficient gene knockout and over-expression vectors for engineering in

2.

Streptomyces. (J Microbiol Biotechnol, 2010, first author)

Research Interests:

a. Biology: Biochemistry, Molecular Biology, Cell Biology.

b. Disease: Osteosarcoma and other cancer related research, Fatty acid metabolism disease.

c. Stem cells: Embryonic stem cells, Mesenchymal stem cells

Professional skills:

1. Laboratory research skills in Biochemistry, Molecular Biology, and Cell Biology

Have experiences in most of laboratory techniques of modern Molecular Biology, Biochemistry,

and Cell Biology as reflected from my peer-reviewed publications. These include, just to name a few,

Molecular cloning; Sequence analysis, annotation and functional characterization of DNA, RNA and

proteins; Expression and purification of recombinant proteins; Lentivirus or retrovirus based gene

knocking down or over-expression; Flow cytometry; Chip-Seq; RNA-Seq; Generation of cell culture

models and development of cell-based assays; Generation of genetically-modified animal models for

physiologic studies.

2. Embryonic Stem Cell Biology

I’m familiar with isolating and culturing mouse embryonic stem (ES) cells, reprogramming

Yunlong He – CV and Bibliography

somatic cells into induced pluripotent stem cells (iPSC), screening and validating targeted ES clones

for injection into blastocysts, and identifying mouse lines with germ-line transmission of the modified

genes.

3. Mesenchymal Stem Cell Biology

I have hands-on experience in mouse mesenchymal stem cells (MSCs), including isolating

MSCs from bone marrow by flow cytometry based cell sorting; culturing and differentiating MSCs

into different lineages in vivo and in vitro; and mouse injection for in vivo studies.

Awards and Honors:

1. Winner of Fellows Award for Research Excellence (FARE) 2013

2. Editorial Board for the Journal of Cancer Biology & Treatment (CBT) since 2014

3. Chief Judge for Stem Cells-General Section of FARE 2014 Travel Award Competition

4. Active Judge for Stress, Aging and Oxidative Stress/Free Radical Research Section of FARE

2015 Travel Award Competition

5. Associate Member of American Association for Cancer Research (AACR) since 2012

6. Active Member of Society of Chinese Bioscientists in America (SCBA) since 2012

Publications:

1. He Y, Dubios W, Yang H, Jiang S, Mishra P, Ren L, Gou H, Lal A, Khanna C, Merlino G, Lee M,

Huang J. p53 loss increases the heterogeneity and osteogenic differentiation of mesenchymal stem

cells. Stem cells. (undergoing review, 2014)

2. Shin MH, He Y, Huang J. Embryonic stem cells shed new light on the developmental roles of p53.

Cell & Bioscience. Oct 9, 2013, 3:42

3. Zhang X*, He Y*, Lee KH, Dubois W, Li Z, Wu X, Kovalchuk A, Zhang W and Huang J. Rap2b,

a novel p53 target, regulates p53-mediated pro-survival function. Cell Cycle. 12:8, 1279–1291;

April 15, 2013. (*co-first author)

4. Li M, He Y, Dubois W, Wu X, Shi J, Huang J. Distinct regulatory mechanisms and functions of

p53-activated and p53-repressed DNA damage response genes in embryonic stem cells.

Molecular Cell. 46(1):30-42. Apr 13, 2012.

Yunlong He – CV and Bibliography

5. Li M, He Y, Feng X, Huang J. Genome-wide studies of the transcriptional regulation by p53.

Biochim Biophys Acta, Feb 10, 2012.

6. He Y, Korboukh I, Jin J, Huang J. Targeting protein lysine methylation and demethylation in

cancers. Acta Biochim. Biophys. Sin. (Shanghai). 44: 70-9, 2012.

7. Liu F, Barsyte-Lovejoy D, Allali-Hassani A, He Y, Martin M, Chen X, Yates C, Frye S, Brown P,

Huang J, Vedadi M, Arrowsmith C, Jin J. Optimization of Cellular Activity of G9a Inhibitors

7-Aminoalkoxy-quinazolines. Journal of Medicinal Chemistry. 8: 6139, 2011.

8. He Y, Sun Y, Liu T, Zhou X, Bai L, Deng Z. Cloning of the separate meilingmycin biosynthetic

gene clusters through acyltransferase-ketoreductase (AT-KR) di-domain PCR amplification.

Applied and Environment Microbiology. 76(10): 3283-92, 2010.

9. He Y, Wang Z, Bai L, Liang J, Zhou X, Deng Z. Two pHZ1358-derivative vectors for efficient

gene knockout in Streptomyces. Journal of Microbiology and Biotechnology. 20(4): 678-82,

2010.

10. He Y, Zhu D, Bai L, Deng Z. Cloning of antibiotic biosynthetic gene clusters from genomic

library by narrow-down PCR. Journal of Shanghai Jiao Tong University. 43(1): 5-8, 2009.

11. Zhu D, He Y, Bai L, Deng Z. Positive regulation of avermectin biosynthesis by AveR in

Streptomyces avermitilis. Journal of Shanghai Jiao Tong University. 42(9): 1448-1452, 2008.

Contact information for references:

Stuart H. Yuspa, M.D.

Laboratory of Cancer Biology and Genetics

Head, In Vitro Pathogenesis Section

Laboratory Co-Chief

Center for Cancer Research

National Cancer Institute

Phone: 301-***-****

301-***-****

Fax:

E-Mail: *****@***.***

Yunlong He – CV and Bibliography

Curtis C. Harris, M.D.

Laboratory of Human Carcinogenesis

Head, Molecular Genetics and Carcinogenesis Section

Laboratory Chief

Center for Cancer Research

National Cancer Institute

Phone: 301-***-****

301-***-****

Fax:

E-Mail: *************@***.***

Beverly Mock, Ph.D.

Laboratory of Cancer Biology and Genetics

Head, Cancer Genetics Section

Deputy Laboratory Chief

Center for Cancer Research

National Cancer Institute

Phone: 301-***-****

301-***-****

Fax:

E-Mail: *****@****.***.***

Yunlong He – CV and Bibliography



Contact this candidate