TY - JOUR
T1 - Recent advances in spatially resolved transcriptomics
T2 - challenges and opportunities
AU - Lee, Jongwon
AU - Yoo, Minsu
AU - Choi, Jungmin
N1 - Funding Information:
The authors are grateful to Junho Song for critical reading of the manuscript. This research was supported by the National Research Foundation of Korea (NRF) grants funded by the South Korean government (2020R1F1A1076705)
Publisher Copyright:
© 2022. by the The Korean Society for Biochemistry and Molecular Biology
PY - 2022
Y1 - 2022
N2 - Single-cell RNA sequencing (scRNA-seq) has greatly advanced our understanding of cellular heterogeneity by profiling individual cell transcriptomes. However, cell dissociation from the tissue structure causes a loss of spatial information, which hinders the identification of intercellular communication networks and global transcriptional patterns present in the tissue architecture. To overcome this limitation, novel transcriptomic platforms that preserve spatial information have been actively developed. Significant achievements in imaging technologies have enabled in situ targeted transcriptomic profiling in single cells at singlemolecule resolution. In addition, technologies based on mRNA capture followed by sequencing have made possible profiling of the genome-wide transcriptome at the 55-100 μm resolution. Unfortunately, neither imaging-based technology nor capturebased method elucidates a complete picture of the spatial transcriptome in a tissue. Therefore, addressing specific biological questions requires balancing experimental throughput and spatial resolution, mandating the efforts to develop computational algorithms that are pivotal to circumvent technology-specific limitations. In this review, we focus on the current state-of-the-art spatially resolved transcriptomic technologies, describe their applications in a variety of biological domains, and explore recent discoveries demonstrating their enormous potential in biomedical research.
AB - Single-cell RNA sequencing (scRNA-seq) has greatly advanced our understanding of cellular heterogeneity by profiling individual cell transcriptomes. However, cell dissociation from the tissue structure causes a loss of spatial information, which hinders the identification of intercellular communication networks and global transcriptional patterns present in the tissue architecture. To overcome this limitation, novel transcriptomic platforms that preserve spatial information have been actively developed. Significant achievements in imaging technologies have enabled in situ targeted transcriptomic profiling in single cells at singlemolecule resolution. In addition, technologies based on mRNA capture followed by sequencing have made possible profiling of the genome-wide transcriptome at the 55-100 μm resolution. Unfortunately, neither imaging-based technology nor capturebased method elucidates a complete picture of the spatial transcriptome in a tissue. Therefore, addressing specific biological questions requires balancing experimental throughput and spatial resolution, mandating the efforts to develop computational algorithms that are pivotal to circumvent technology-specific limitations. In this review, we focus on the current state-of-the-art spatially resolved transcriptomic technologies, describe their applications in a variety of biological domains, and explore recent discoveries demonstrating their enormous potential in biomedical research.
KW - Integrative computational algorithm
KW - Multimodal data analysis
KW - Single-cell rna sequencing
KW - Spatially resolved transcriptomics
UR - http://www.scopus.com/inward/record.url?scp=85128001011&partnerID=8YFLogxK
U2 - 10.5483/BMBRep.2022.55.3.014
DO - 10.5483/BMBRep.2022.55.3.014
M3 - Article
C2 - 35168703
AN - SCOPUS:85128001011
SN - 1976-6696
VL - 55
SP - 113
EP - 124
JO - BMB Reports
JF - BMB Reports
IS - 3
ER -