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Cooperative contributions of the klf1 and klf17 genes in zebrafish primitive erythropoiesis
Krüppel-like transcription factors (Klfs), which are characterized by the three conserved C-terminal zinc fingers, are involved in various biological processes, such as haematopoiesis and angiogenesis. However, how the Klf family of transcription factors cooperate in organogenesis remains elusive. D...
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Published in: | Scientific reports 2023-08, Vol.13 (1), p.12279-12279, Article 12279 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Krüppel-like transcription factors (Klfs), which are characterized by the three conserved C-terminal zinc fingers, are involved in various biological processes, such as haematopoiesis and angiogenesis. However, how the Klf family of transcription factors cooperate in organogenesis remains elusive. During zebrafish embryogenesis, both
klf1
and
klf17
are expressed in the intermediate cell mass (ICM), where primitive erythroid cells are produced. Using CRISPR–Cas9 genome editing technology, we established
klf1
-
klf17
double mutant zebrafish to investigate the functionally interactive roles of the
klf1
and
klf17
genes. The
klf1
-
klf17
mutant exhibited a diminished number of circulating primitive erythroid cells at 2 days postfertilization (dpf), while
klf1
or
klf17
single mutants and wild-type embryos produced comparable numbers of primitive erythroid cells. Circulating erythroid cells from the
klf1
-
klf17
mutant possessed larger nuclei at 2 dpf than wild-type cells, suggesting the impairment of primitive erythroid cell maturation. The expression of the erythroid cell maturation markers
band3
and
mitoferrin
, but not the haematopoietic progenitor markers
c-myb
and
scl
, was decreased in the
klf1
-
klf17
mutant at 1 dpf. Thus, these results illustrate the cooperative function of
klf1
and
klf17
in the maturation processes of zebrafish primitive erythroid cells. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-023-39196-1 |