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Hou Research

Contact

Name: Ya-Ming Hou, PhD
Position: Professor

233 South 10th Street
BLSB 220
Philadelphia, PA 19107

Contact Number(s):

Recent Publications

 

Comprehensive Peer-Reviewed Publications via Scopus

2019

  1. Morelli, KH, Griffin, LB, Pyne, NK, Wallace, LM, Fowler, AM, Oprescu, SN, Takase, R, Wei, N, Meyer-Schuman, R, Mellacheruvau, D, Kitzman, JO, Kocen, SG, Lupski, JR, Nesvizhskii, A, Mancias, P, Butler, I, Yang, XL, Hou, YM, Antonellis, A, Harper, SQ, Burgress, RW. (2019) Allele-specific RNA interference: Precision gene therapy for dominant inherited neuropathy. J. Clinical Investigation 129: 5568-5583. PMID: 31557132; PMCID:PMC6877339. 
  2. Yin S, Dhital B, Hou YM. How to Untie a Protein Knot. Structure, 2019.
  3. Kuo ME, Theil AF, Kievit A, Malicdan MC, Introne WJ, Christian T, Verheijen FW, Smith DEC, Mendes MI, Hussaarts-Odijk L, van der Meijden E, van Slegtenhorst M, Wilke M, Vermeulen W, Raams A, Groden C, Shimada S, Meyer-Schuman R, Hou YM, Gahl WA, Antonellis A, Salomons GS, Mancini GMS. Cysteinyl-tRNA Synthetase Mutations Cause a Multi-System, Recessive Disease That Includes Microcephaly, Developmental Delay, and Brittle Hair and Nails. Am J Hum Genet. 7 March 2019.
  4. Masuda I, Matsubara R, Christian T, Rojas ER, Yadavalli SS, Zhang L, Goulian M, Foster L, Huang KC, Hou YM. tRNA Methylation Is a Global Determinant of Bacterial Multi-drug Resistance. Cell Systems 10 April 2019.
  5. Sun C, Song J, Jiang Y, Zhao C, Lu J, Li Y, Wang Y, Gao M, Xi J, Luo S, Li M, Donaldson K, Oprescu SN, Slavin TP, Lee S, Magoulas PL, Lewis AM, Emrick L, Lalani SR, Niu Z, Landsverk ML, Walkiewicz M, Person RE, Mei H, Rosenfeld JA, Yang Y, Antonellis A, Hou YM, Lin J, Zhang VW. Loss-of-function mutations in Lysyl-tRNA synthetase cause various leukoencephalopathy phenotypes. Neurology Genetics. April 2019.
  6. Hou YM, Masuda I, Gamper H. (2019) Codon-Specific Translation by m1G37 Methylation of tRNA. Front. Genet. 10 January 2019

2018

  1. Masuda, I, Takase, R, Matsubara, R, Paulines, MJ, Gamper, H, Limbach, PA, Hou, YM. (2018) Selective terminal methylation of a tRNA wobble base. Nucleic Acids Res, 46 (7):e37.

  2. Weterman, MAJ, Kuo, M, Kenter, SB, Gordillo, S, Karjosukarso, D, Takase, R, Bronk, M, Oprescu, S, de Wissel, M, van Ruissen, F, Breuning, M, Hou, YM, de Visser, M, Antonellis, A, Baas, F. (2018) Hypermorphic and hypomorphic AARS alleles in patients with CMT2N expands clinical and molecular heterogeneities. Human Molecular Genetics, in press.

  3. Gamper, H, Hou, YM. (2018) tRNA 3'-amino-tailing for stable amino acid attachment. RNA.

  4. Kwon NH, Lee JY, Ryu YL, Kim C, Kong J, Oh S, Kim SH, Ahn SG, Jeong J, Kim HK, Kim JH, Han DY, Park MC, Takase R, Masuda I, Hou YM, Jang SI, Chang YS, Lee DK, Guo M, Kang BS, Wang MW, Basappa B, Lee JH, Kim S.  (2018) Stabilization of cyclin dependent kinase 4 by methionyl-tRNA synthetase in p16INK4a-negative cancer. ACS Pharmacology & Translational Science, 1, 21-31.

2017

  1. Fan H, Conn AB, Williams PB, Diggs S, Hahm J, Gamper HB Jr, Hou YM, O'Leary SE, Wang Y, Blaha GM. Transcription-translation coupling: direct interactions of RNA polymerase with ribosomes and ribosomal subunits. Nucleic Acids Res. 2017 Nov.

  2. Oprescu SN, Chepa-Lotrea X, Takase R, Golas G, Markello TC, Adams DR, Toro C, Gropman AL, Hou YM, Malicdan MCV, Gahl WA, Tifft CJ, Antonellis A. Compound heterozygosity for loss-of-function GARS variants results in a multisystem developmental syndrome that includes severe growth retardation. Hum Mutat. 2017 Oct.

  3. Hou YM, Matsubara R, Takase R, Masuda I, Sulkowska JI. TrmD: A Methyl Transferase for tRNA Methylation With m1G37. Enzymes. 41:89-115. 2017.

  4. Po P, Delaney E, Gamper H, Szantai-Kis DM, Speight L, Tu L, Kosolapov A, Petersson EJ, Hou YM, Deutsch C. Effect of Nascent Peptide Steric Bulk on Elongation Kinetics in the Ribosome Exit Tunnel. J Bol Miol. 429(12):1873-1888. Jun16 2017.

  5. Masuda I, Igarashi T, Sakaguchi R, Nitharwal RG, Takase R, Han KY, Leslie BJ, Liu C, Gamper H, Ha T, Sanyal S, Hou YM. A genetically encoded fluorescent tRNA is active in live-cell protein synthesis. Nucleic Acids Res. Apr 20, 2017

2016

  1. Gall AR, Datsenko KA, Figueroa-Bossi N, Bossi L, Masuda I, Hou YM, Csonka LN. Mg2+ regulates transcription of mgtA in Salmonella Typhimurium via translation of proline codons during synthesis of the MgtL peptide. Proc Natl Acad Sci USA. Dec 27 2016.
  2. Ardell DH, Hou YM. Initiator tRNA genes template the 3' CCA end at high frequencies in bacteria. BMC Genomics. 8 Dec 2016
  3. Sakaguchi R, Hou YM. (2016) タンパク質の結び目構造からのシグナルによるtRNAのメチル化修飾. DOI:10.7875/first.author.2016.097.. First Author's
  4. Christian T, Sakaguchi R, Perlinska AP, Lahoud G, Ito T, Taylor EA, Yokoyama S, Sulkowska JI, Hou YM. Methyl transfer by substrate signaling from a knotted protein fold.. Nat Struct Mol Biol. Aug 29, 2016
  5. Liu C, Stonestrom AJ, Christian T, Yong J, Takase R, Hou YM, Yang X. Molecular Basis and Consequences of the Cytochrome c-tRNA Interaction.. J Biol Chem, 291, 10426-36. May 6, 2016
  6. Falk MJ, Gai X, Shigematsu M, Vilardo E, Takase R, McCormick E, Christian T, Place E, Pierce EA, Consugar M, Gamper HB, Rossmanith W, Hou YM. A novel HSD17B10 mutation impairing the activities of the mitochondrial RNase P complex causes X-linked intractable epilepsy and neurodevelopmental regression.. RNA Biol, 13, 477-85 . May 3, 2016

2015

  1. Ito, T, Masuda, I, Yoshida, K, Goto-Ito, S, Suh, SW, Hou, YM, Yokoyama, S. Structural mechanism of site-specific RNA modification by the bacterial tRNA(m1G37)-methyltransferase TrmD. Proc Natl Acad Sci, 112, E4197-204. Aug 4 2015

  2. Gamper, H, Masuda, I, Frenkel-Morgenstern, M, Hou, YM. The UGG isoacceptor of tRNAPro is naturally prone to frameshifts. Int J. Mol Sci. 16, 14866-14883. Jul 1, 2015

  3. Hou, YM, Gamper, H, Yang, W. (2015) Post-transcriptional modifications of tRNA – A response to the genetic code degeneracy. RNA 21, 642-644. Apr 2015

  4. Hou, YM, Masuda, I. (2015) Kinetic analysis of tRNA methyltransferases. Methods in Enzymology. Edited by Chuan He, 560, 91-116.

  5. Gamper HB, Masuda I, Frenkel-Morgenstern M, Hou YM, Maintenance of protein synthesis reading frame by EF-P and m1G37-tRNAAm J Human Benetics96(4):675-81. doi: 10.1016, April2, 2015

  6. Ya-Ming Hou et al., Loss-of-Function Alanyl-tRNA Synthetase Mutations Cause an Autosomal-Recessive Early-Onset Epileptic Encephalopathy with Persistent Myelination DefectAm J Human Genetics96(4):675-81. doi: 10.1016, April2, 2015