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Finer resolution analysis of transcriptional programming during the active migration of chicken primordial germ cells
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Title
Finer resolution analysis of transcriptional programming during the active migration of chicken primordial germ cells
Issued Date
2022-11
Citation
Rengaraja, Deivendran. (2022-11). Finer resolution analysis of transcriptional programming during the active migration of chicken primordial germ cells. Computational and Structural Biotechnology Journal, 20, 5911–5924. doi: 10.1016/j.csbj.2022.10.034
Type
Article
Author Keywords
ChickenPGCsMigrationSingle-cell RNA sequencingSex differencesTranscription factors
Keywords
FAMILY-MEMBERSSMALL RNASEXPRESSIONDAZLGENEPLURIPOTENCYDYNAMICSHOMOLOGPROTEINDIFFERENTIATION
ISSN
2001-0370
Abstract
Primordial germ cells (PGCs) in chickens polarize and move passively toward the anterior region by the morphogenetic movement of the embryo. Further migration of PGCs towards the genital ridge via the germinal crescent region and blood vessels occurs actively through the chemoattractive signals. The mechanisms of initiation of PGCs migration, lodging the PGCs in the vascular system, and colonization of PGCs in the gonads are well-studied. However, transcriptome sequencing-based cues directing the migration of the PGCs towards gonads, some of the relevant molecules, biological processes, and transcription factors (TFs) are less studied in chickens. The current study comprehensively interprets the transcriptional programming of PGCs during their active migration (E2.5 to E8). Current results revealed several vital understandings, including a set of genes that upregulated male-specifically (XPA, GNG10, RPL17, RPS23, and NDUFS4) or female-specifically (HINTW, NIPBL, TERAL2, ATP5F1AW, and SMAD2W) in migrating PGCs, and transcriptionally distinct PGCs, particularly in the gonadal environment. We identified DNA methylation and histone modification-associated genes that are novel in chicken PGCs and show a time-dependent enrichment in migrating PGCs. We further identified a large number of differentially expressed genes (DEGs, including TFs) in blood PGCs (at E2.5) compared to gonadal PGCs (at E8) in both sexes; however, this difference was greater in males. We also revealed the enriched biological processes and signaling pathways of significant DEGs identified commonly, male-specifically, or female-specifically between the PGCs isolated at E2.5, E6, and E8. Collectively, these analyses provide molecular insights into chicken PGCs during their active migration phase. © 2022 The Author(s)
URI
http://hdl.handle.net/20.500.11750/17487
DOI
10.1016/j.csbj.2022.10.034
Publisher
Elsevier B.V.
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