Minoru S.H. Ko

ORCID: 0000-0002-3530-3015
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About
Contact & Profiles
Research Areas
  • Pluripotent Stem Cells Research
  • CRISPR and Genetic Engineering
  • Animal Genetics and Reproduction
  • Reproductive Biology and Fertility
  • RNA Research and Splicing
  • Genomics and Chromatin Dynamics
  • Renal and related cancers
  • Gene expression and cancer classification
  • Molecular Biology Techniques and Applications
  • Epigenetics and DNA Methylation
  • Prenatal Screening and Diagnostics
  • 3D Printing in Biomedical Research
  • RNA and protein synthesis mechanisms
  • Chromosomal and Genetic Variations
  • Gene Regulatory Network Analysis
  • Genetic Syndromes and Imprinting
  • RNA modifications and cancer
  • Genetic Mapping and Diversity in Plants and Animals
  • Genetics, Aging, and Longevity in Model Organisms
  • Bioinformatics and Genomic Networks
  • Single-cell and spatial transcriptomics
  • Viral Infectious Diseases and Gene Expression in Insects
  • Virus-based gene therapy research
  • SARS-CoV-2 and COVID-19 Research
  • RNA Interference and Gene Delivery

Elixir Medical (United States)
2023-2025

Keio University
2014-2023

Centre d'Immunologie et des Maladies Infectieuses
2023

Keio University Hospital
2013-2017

National Institute on Aging
2007-2016

National Institutes of Health
2006-2016

Johns Hopkins University
2005-2015

Chinese Academy of Fishery Sciences
2015

Institute on Aging
2004-2013

Japan Science and Technology Agency
2013

Degradation of mRNA is one the key processes that control steady-state level gene expression. However, rate decay for majority genes not known. We successfully obtained 19 977 non-redundant by microarray analysis RNA samples from mouse embryonic stem (ES) cells. Median estimated half-life was 7.1 h and only <100 genes, including Prdm1, Myc, Gadd45 g, Foxa2, Hes5 Trib1, showed less than 1 h. In general, species with short were enriched among regulatory functions (transcription factors),...

10.1093/dnares/dsn030 article EN cc-by-nc DNA Research 2008-11-17
Daniela S. Gerhard Lukas Wagner Elise A. Feingold Carolyn M. Shenmen Lynette Grouse and 95 more Greg Schuler Steven L. Klein Susan Old Rebekah S. Rasooly Peter J. Good Mark S. Guyer Allison M. Peck Jeffery G. Derge David J. Lipman Francis S. Collins Wonhee Jang Stephen T. Sherry Mike Feolo Leonie Misquitta Eduardo Lee Kirill E. Rotmistrovsky Susan F. Greenhut Carl F. Schaefer Kenneth H. Buetow Tom I. Bonner David Haussler Jim Kent Mark Diekhans Terrence S. Furey Michael R. Brent Christa Prange Kirsten Schreiber Nicole Shapiro Narayan Bhat Ralph F. Hopkins Florence Hsie Tom Driscoll Marcelo B. Soares Maria F. Bonaldo T.L. Casavant Todd E. Scheetz Michael Brownstein Ted B. Usdin Toshiyuki Shiraki Piero Carninci Yulan Piao Dawood B. Dudekula Minoru S.H. Ko Koichi Kawakami Yutaka Suzuki Sumio Sugano C. E. Gruber M. Smith Blake A. Simmons Troy Moore Richard Waterman Stephen L. Johnson Yijun Ruan Chia Lin Wei Sinnakaruppan Mathavan Preethi H. Gunaratne Jiaqian Wu Angela Garcia Stephen W. Hulyk Edwin Fuh Ye Yuan Anna Sneed Carla Kowis Anne V. Hodgson Donna M. Muzny John D. McPherson Richard A. Gibbs Jessica Fahey Erin Helton Mark Ketteman Anuradha Madan Stephanie Rodrigues Amy Sanchez Michelle Whiting Anup Madan Alice Young Keith Wetherby Stephen J. Granite Peggy N. Kwong Charles P. Brinkley Russell L. Pearson Gerard G. Bouffard Robert W. Blakesly Eric D. Green Mark Dickson Álex Rodríguez Jonathan Wood Jeremy Schmutz R Myers Yaron S.N. Butterfield Malachi Griffith Obi L. Griffith Martin Krzywinski Nancy Liao Ryan Morrin

The National Institutes of Health's Mammalian Gene Collection (MGC) project was designed to generate and sequence a publicly accessible cDNA resource containing complete open reading frame (ORF) for every human mouse gene. initially used random strategy select clones from large number libraries diverse tissues. Candidate were chosen based on 5′-EST sequences, then fully sequenced high accuracy analyzed by algorithms developed this project. Currently, more than 11,000 10,000 genes are...

10.1101/gr.2596504 article EN cc-by-nc Genome Research 2004-10-15

Decreasing oocyte competence with maternal aging is a major factor in human infertility. To investigate the age-dependent molecular changes mouse model, we compared expression profiles of metaphase II oocytes collected from 5- to 6-week-old mice those 42- 45-week-old using NIA 22K 60-mer oligo microarray. Among approximately 11 000 genes whose transcripts were detected oocytes, about 5% (530) showed statistically significant changes, excluding possibility global decline transcript abundance....

10.1093/hmg/ddh241 article EN Human Molecular Genetics 2004-08-18

We present the AGEMAP (Atlas of Gene Expression in Mouse Aging Project) gene expression database, which is a resource that catalogs changes as function age mice. The database includes for 8,932 genes 16 tissues age. found great heterogeneity amount transcriptional with different tissues. Some displayed large differences old mice, suggesting these may contribute strongly to organismal decline. Other showed few or no age, indicating strong levels homeostasis throughout life. Based on pattern...

10.1371/journal.pgen.0030201 article EN cc-by PLoS Genetics 2007-11-28

cDNA microarray technology has been increasingly used to monitor global gene expression patterns in various tissues and cell types. However, applications mammalian development have hampered by the lack of appropriate collections, particularly for early developmental stages. To overcome this problem, a PCR-based library construction method was derive 52,374 expressed sequence tags from pre- peri-implantation embryos, embryonic day (E) 12.5 female gonad/mesonephros, newborn ovary. From these...

10.1073/pnas.97.16.9127 article EN Proceedings of the National Academy of Sciences 2000-08-01

The analysis of RNA-Seq data from individual differentiating cells enables us to reconstruct the differentiation process and degree (in pseudo-time) each cell. Such analyses can reveal detailed expression dynamics functional relationships for differentiation. To further elucidate processes, more insight into gene regulatory networks is required. pseudo-time be regarded as time information and, therefore, single-cell are time-course with high resolution. Although useful inferring networks,...

10.1093/bioinformatics/btx194 article EN cc-by Bioinformatics 2017-04-02

B-type lamins, the major components of nuclear lamina, are believed to be essential for cell proliferation and survival. We found that mouse embryonic stem cells (ESCs) do not need any lamins self-renewal pluripotency. Although genome-wide lamin-B binding profiles correlate with reduced gene expression, such is directly required silencing in ESCs or trophectoderm cells. However, proper organogenesis. Defects spindle orientation neural progenitor migration neurons probably cause brain...

10.1126/science.1211222 article EN Science 2011-11-25

Embryonic stem cells (ESCs) are derived from mammalian embryos during the transition totipotency, when individual blastomeres can make all lineages, to pluripotency, they competent only embryonic lineages. ESCs maintained with inhibitors of MEK and GSK3 (2i) thought represent an embryonically restricted ground state. However, we observed heterogeneous expression extraembryonic endoderm marker Hex in 2i-cultured embryos, suggesting that 2i blocked development prior epiblast commitment....

10.1016/j.celrep.2013.04.034 article EN cc-by-nc-nd Cell Reports 2013-06-01

Loss of imprinting (LOI) the insulin-like growth factor II gene ( IGF2 ) is an epigenetic alteration that results in a modest increase expression, and it present normal colonic mucosa about 30% patients with colorectal cancer. To investigate its role intestinal tumorigenesis, we created mouse model Igf2 LOI by crossing female H19 +/– mice male Apc +/Min mice. Mice developed twice as many tumors did control littermates. Notably, these also showed shift toward less differentiated epithelium,...

10.1126/science.1108080 article EN Science 2005-02-25

Mouse Tabby ( Ta ) and X chromosome-linked human EDA share the features of hypoplastic hair, teeth, eccrine sweat glands. We have cloned gene find it to be homologous gene. The is altered in two alleles with a point mutation or deletion. expressed developing teeth epidermis; no expression seen corresponding tissues from mice. genes both encode alternatively spliced forms; novel exons now extend 3′ end All transcripts recovered same 5′ exon. longest cDNA encodes 391-residue transmembrane...

10.1073/pnas.94.24.13069 article EN Proceedings of the National Academy of Sciences 1997-11-25

Delayed implantation (embryonic diapause) occurs when the embryo at blastocyst stage achieves a state of suspended animation. During this period, growth is very slow, with minimal or no cell division. Nearly 100 mammals in seven different orders undergo delayed implantation, but underlying molecular mechanisms that direct process remain largely unknown. In mice, ovariectomy before preimplantation ovarian estrogen secretion on day 4 pregnancy initiates dormancy, which normally lasts for 1–2...

10.1073/pnas.0402597101 article EN Proceedings of the National Academy of Sciences 2004-07-01

We have developed a program for microarray data analysis, which features the false discovery rate testing statistical significance and principal component analysis using singular value decomposition method detecting global trends of gene-expression patterns. Additional include variance with multiple methods error adjustment, correction cross-channel correlation two-color microarrays, identification genes specific to each cluster tissue samples, biplot tissues corresponding tissue-specific...

10.1093/bioinformatics/bti343 article EN Bioinformatics 2005-02-25

ABSTRACT Little is known about gene action in the preimplantation events that initiate mammalian development. Based on cDNA collections made from each stage egg to blastocyst, 25438 3′-ESTs were derived, and represent 9718 genes, half of them novel. Thus, a considerable fraction genes dedicated embryonic expression. This study reveals profound changes expression include transient induction transcripts at stage. These results raise possibility development driven by series stage-specific...

10.1242/dev.127.8.1737 article EN Development 2000-04-15

Although the POU transcription factor Oct3/4 is pivotal in maintaining self renewal of embryonic stem (ES) cells, little known its molecular mechanisms. We previously reported that N-terminal transactivation domain required for activation Lefty1 expression (H. Niwa, S. Masui, I. Chambers, A. G. Smith, and J. Miyazaki, Mol. Cell. Biol. 22:1526-1536, 2002). Here we test whether a direct target Oct3/4. identified an ES cell-specific enhancer upstream promoter contains binding sites Sox2. Unlike...

10.1128/mcb.00468-06 article EN Molecular and Cellular Biology 2006-10-01

ES cells are defined as self-renewing, pluripotent cell lines derived from early embryos. Cultures of also characterized by the expression certain markers thought to represent state. However, despite widespread key such Oct4 and appearance a characteristic undifferentiated morphology, functional may only small fraction cultures grown under self-renewing conditions. Thus phenotypically "undifferentiated" consist heterogeneous population functionally distinct types. Here we use transgenic...

10.1371/journal.pbio.1000379 article EN cc-by PLoS Biology 2010-05-25

Large-scale gene expression profiling was performed on embryo-derived stem cell lines to identify molecular signatures of pluripotency and lineage specificity. Analysis pluripotent embryonic (ES) cells, extraembryonic-restricted trophoblast (TS) terminally-differentiated mouse embryo fibroblast (MEF) cells identified profiles unique each type, as well genes common only ES TS cells. Whereas most the MEF-specific had been characterized previously, majority (67%) ES-specific were novel did not...

10.1101/gr.670002 article EN cc-by-nc Genome Research 2002-12-01

10.1016/s0022-5193(05)80421-7 article EN Journal of Theoretical Biology 1991-11-01
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